Prof.Dr. TÜLAY GÜRAN
Tıp Fakültesi / Dahili Tıp Bilimleri Bölümü

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Marmara Üniversitesi - Tıp Fakültesi / Dahili Tıp Bilimleri Bölümü / Oda No (Belirtilmemiş)
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YAYINLAR & ESERLER
MAKALELER
ULUSLARARASI
SCI, SSCI, AHCI İNDEKSLERİNE GİREN DERGİLERDE YAYINLANAN MAKALELER
1. EREN ERDAL,ERGÜR AYÇA,İŞGÜVEN ŞÜKRİYE PINAR,Çelebi Bitkin Eda,BERBEROĞLU MERİH,ŞIKLAR ZEYNEP,BAŞ FİRDEVS,BEREKET ABDULLAH,Turan Serap,SAĞLAM HALİL,ATAY ZEYNEP,ERCAN OYA,GÜRAN TÜLAY,ATABEK MEHMET EMRE,Korkmaz Hüseyin Anıl,KILINÇ UĞURLU AYLİN,AKINCI AYŞEHAN,DÖĞER ESRA,ŞİMŞEK ENVER,DEMET AKBAŞ EMİNE,ABACI AYHAN,Gül Ülkü,Acar Sezer,Mengen Uçaktürk Eda,Unal Edip,TARIM ÖMER FARUK. Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey. Journal of Clinical Research in Pediatric Endocrinology. 2018. (Yayına Ulaşmak İçin Tıklayınız)
2. ÇETİNKAYA SEMRA,GÜRAN TÜLAY,KURNAZ ERDAL,Keskin Melikşah,Sağsak Elif,Suntharalingham Jenifer P,Savaş Erdeve Senay,Buonocore Federica,Achermann John C,Aycan Zehra. A Patient with Proopiomelanocortin Deficiency: An Increasingly Important Diagnosis to Make. Journal of Clinical Research in Pediatric Endocrinology. Cilt 10. sf 68-73, 2018. (Yayına Ulaşmak İçin Tıklayınız)
3. Haliloğlu Belma,Abalı Saygın,Buğrul Fuat,Çelik Enes,Baş Serpil,ATAY ZEYNEP,GÜRAN TÜLAY,DEMİRCİOĞLU SERAP,BEREKET ABDULLAH. The Distribution of Different Types of Diabetes in Childhood: A Single Center Experience. Journal of Clinical Research in Pediatric Endocrinology. Cilt 10. sf 125-130, 2018. (Yayına Ulaşmak İçin Tıklayınız)
4. AYDIN BANU,SAKA NURÇİN,BAŞ FİRDEVS,YILMAZ Y,HALİLOĞLU BELMA,GÜRAN TÜLAY,TURAN SERAP,BEREKET ABDULLAH,YEŞİLTEPE MUTLU GÜL,ÇİZMECİOĞLU FİLİZ MİNE,HATUN ŞÜKRÜ,BEZEN DİĞDEM,TÜTÜNCÜLER FİLİZ,CEBECİ NURDAN,İŞGÜVEN ŞÜKRİYE PINAR,MEMİOĞLU NİHAL,ERCAN OYA,POYRAZOĞLU ŞÜKRAN,BUNDAK RÜVEYDE,DARENDELİLER FATMA FEYZA. Evaluation and Treatment Results of Ovarian Cysts in Childhood and Adolescence: A Multicenter, Retrospective Study of 100 Patients. Journal of Pediatric and Adolescent Gynecology. Cilt 30. sf 449-455, 2017. (Yayına Ulaşmak İçin Tıklayınız)
5. Sunter Gulin,Enver Ece Oge,Akbarzade Azad,Turan Serap,Vatansever Pinar,Gunal Dilek Ince,Haklar Goncagul,Agan Kadriye,GÜRAN TÜLAY. Acquired modification of sphingosine-1-phosphate lyase activity is not related to adrenal insufficiency. BMC Neurology. Cilt 18. 2018. (Yayına Ulaşmak İçin Tıklayınız)
6. GÜRAN TÜLAY,Tezel Başak,Gürbüz Fatih,Eklioğlu Beray Selver,Hatipoğlu Nihal,Kara Cengiz,Aydın Murat,Simşek Enver,Çizmecioğlu Filiz Mine,Ozon Alev. Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants. Journal of Clinical Research in Pediatric Endocrinology. 2018. (Yayına Ulaşmak İçin Tıklayınız)
7. POYRAZOĞLU ŞÜKRAN,Bundak Rüveyda,YAVAŞ ABALI ZEHRA,ÖNAL HASAN,Sarıkaya Sevil,Akgün Abdurrahman,Baş Serpil,ABALI SAYGIN,BEREKET ABDULLAH,EREN ERDAL,TARIM ÖMER FARUK,GÜVEN AYLA,Yıldız Metin,Karaman Aksakal Derya,Yüksel Ayşegül,Seymen Karabulut Gülcan,HATUN ŞÜKRÜ,ÖZGEN İLKER TOLGA,CESUR YAŞAR,Azizoğlu Mehmet,DİLEK EMİNE,TÜTÜNCÜLER FİLİZ,Papatya Çakır Esra,Özcabı Bahar,EVLİYAOĞLU SAADET OLCAY,Karadeniz Songül,Dursun Fatma,Bolu Semih,ARSLANOĞLU İLKNUR,YEŞİLTEPE MUTLU RAHİME GÜL,Kırmızıbekmez Heves,İŞGÜVEN ŞÜKRİYE PINAR,Üstyol Ala,ADAL SERVET ERDAL,Uçar Ahmet,CEBECİ AYŞE NURCAN,Bezen Didem,BİNAY ÇİĞDEM,SEMİZ SERAP,Korkmaz Hüseyin Anıl,Memioğlu Nihal,Sağsak Elif,Nur Peltek Havva,Yıldız Melek,Akçay Teoman,Turan Serap,GÜRAN TÜLAY,Atay Zeynep,Akçan Neşe,ÇİZMECİOĞLU FİLİZ MİNE,ERCAN OYA,DAĞDEVİREN ÇAKIR AYDİLEK,BAŞ FİRDEVS,İŞSEVER HALİM,DARENDELİLER FATMA FEYZA. Incidence of Type 1 Diabetes in Children Aged Below 18 Years During 2013-2015 in Northwest Turkey. Journal of Clinical Research in Pediatric Endocrinology. Cilt 10. sf 336-342, 2018. (Yayına Ulaşmak İçin Tıklayınız)
8. ÇETİNKAYA SEMRA,GÜRAN TÜLAY,KURNAZ ERDAL,keskin meliksah,SAVAŞ ERDEVE ŞENAY,Suntharalingham Jenifer P,Buonocore Federica,Achermann John,AYCAN ZEHRA. The description of a new case with proopiomelanocortin (POMC) deficiency: an increasingly important diagnosis to make. Journal of Clinical Research in Pediatric Endocrinology. 2017. (Yayına Ulaşmak İçin Tıklayınız)
9. Prasad Rathi,Hadjidemetriou Irene,Maharaj Avinaash,Meimaridou Eirini,Buonocore Federica,Saleem Moin,Hurcombe Jenny,Bierzynska Agnieszka,Barbagelata Eliana,Bergadá Ignacio,Cassinelli Hamilton,Das Urmi,Krone Ruth,Hacihamdioglu Bulent,Sari Erkan,Yesilkaya Ediz,Storr Helen L,Maria Clemente,Fernandez-Cancio Monica,Camats Nuria,Ram Nanik,Achermann John C,Van Veldhoven Paul,Guasti Leonardo,Braslavsky Debora,GÜRAN TÜLAY,Metherell Louise A. Sphingosine-1-phosphate lyase mutations cause primary adrenal insufficiency and steroid-resistant nephrotic syndrome. Journal of Clinical Investigation. Cilt 127. sf 942-953, 2017. (Yayına Ulaşmak İçin Tıklayınız)
10. Eachus Helen,Zaucker Andreas,Oakes JA,Griffin Aliesha,Weger Meltem,GÜRAN TÜLAY,Taylor Angela,Harris Abigail,Greenfield Andy,Quanson Jonathan L,Storbeck Karl-Heinz,Cunliffe Vincent T,Müller Ferenc,Krone Nils. Genetic Disruption of 21-Hydroxylase in Zebrafish Causes Interrenal Hyperplasia. Endocrinology. Cilt 158. sf 4165-4173, 2017. (Yayına Ulaşmak İçin Tıklayınız)
11. GÜRAN TÜLAY. Latest Insights on the Etiology and Management of Primary Adrenal Insufficiency in Children.. Journal of Clinical Research in Pediatric Endocrinology. 2017. (Yayına Ulaşmak İçin Tıklayınız)
12. SAVAŞ ERDEVE ŞENAY,ÇETİNKAYA SEMRA,Abali Zehra Yavas,POYRAZOĞLU ŞÜKRAN,BAŞ FİRDEVS,BERBEROĞLU MERİH,ŞIKLAR ZEYNEP,Korkmaz Özlem,DERYA BULUŞ,Akbaş Emine Demet,GÜRAN TÜLAY,BÖBER ECE,Akın Onur,Gülay Can Yılmaz,AYCAN ZEHRA. Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height. Journal of Pediatric Endocrinology and Metabolism. Cilt 30. 2017. (Yayına Ulaşmak İçin Tıklayınız)
13. SAVAS ERDEVE SENAY,CETİNKAYA SEMRA,YAVAŞ ABALI ZEHRA,POYRAZOĞLU ŞÜKRAN,BAŞ FİRDEVS,BERBEROĞLU MERİH,ŞIKLAR ZEYNEP,KORKMAZ ÖZLEM,BULUŞ DERYA,AKBAŞ ED,GÜRAN TÜLAY,BÖBER ECE,AKIN O,YILMAZ GC,AYCAN ZEHRA. Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height. Journal of Pediatric Endocrinology and Metabolism. Cilt 30. sf 759-766, 2017. (Yayına Ulaşmak İçin Tıklayınız)
14. AYDIN KÜÇÜKEMRE BANU,SAKA NURÇİN,BAŞ FİRDEVS,YILMAZ YASİN,HALİLOĞLU BELMA,GÜRAN TÜLAY,TURAN SERAP,BEREKET ABDULLAH,YEŞİLTEPE MUTLU GÜL,ÇİZMECİOĞLU FİLİZ MİNE,HATUN ŞÜKRÜ,BEZEN DİDEM,TÜTÜNCÜLER FİLİZ,CEBECİ AYŞE NURCAN,İŞGÜVEN ŞÜKRİYE PINAR,MEMİOĞLU NİHAL,ERCAN OYA,POYRAZOĞLU ŞÜKRAN,BUNDAK RÜVEYDE,DARENDELİLER FATMA FEYZA. Evaluation and Treatment Results of Ovarian Cysts in Childhood and Adolescence: A Multicenter, Retrospective Study of 100 Patients. Journal of Pediatric and Adolescent Gynecology. Cilt 30. sf 449-455, 2017. (Yayına Ulaşmak İçin Tıklayınız)
15. ÇETİNKAYA SEMRA,GÜRAN TÜLAY,Kurnaz Erdal,Keşkin Melikşah,Sağsak Elif,Erdeve Senay Savaş,Suntharalingham Jenifer P,Buonocore Federica,AYCAN ZEHRA. The description of a new case with proopiomelanocortin (POMC) deficiency: an increasingly important diagnosis to make. Journal of Clinical Research in Pediatric Endocrinology. 2017. (Yayına Ulaşmak İçin Tıklayınız)
16. Aydın Banu,Saka Nurçin,BAŞ FİRDEVS,YILMAZ RAVZA SÜMEYYE,HALİLOĞLU BELMA,GÜRAN TÜLAY,TURAN SERAP,BEREKET ABDULLAH,Yeşiltepe Gül,ÇİZMECİOĞLU FİLİZ MİNE,HATUN ŞÜKRÜ,Bezen Diğdem,TÜTÜNCÜLER FİLİZ,CEBECİ AYŞE NURCAN,İŞGÜVEN ŞÜKRİYE PINAR,Memioğlu Nihal,ERCAN OYA,POYRAZOĞLU ŞÜKRAN,BUNDAK RÜVEYDE,DARENDELİLER FATMA FEYZA. Evaluation and Treatment Results of Ovarian Cysts in Childhood and Adolescence: A Multicenter, Retrospective Study of 100 Patients. Journal of Pediatric and Adolescent Gynecology. Cilt 30. sf 449-455, 2017. (Yayına Ulaşmak İçin Tıklayınız)
17. kashyap a patel,colclough kevin,özbek mehmet nuri,yıldız melek,GÜRAN TÜLAY,koçyiğit cemil,ACAR SEZER,ŞIKLAR ZEYNEP,ATAR MÜGE,Johnson Matthew B,Flanagan Sarah E,Ellard Sian,ÇİZMECİOĞLU FİLİZ MİNE,BERBEROĞLU MERİH,DEMİR KORCAN,ÇATLI GÖNÜL,BAŞ SERPİL,akçay teoman,DEMİRBİLEK HÜSEYİN,weedon michael N,Hattersley Andrew T. Comprehensive genetic testing shows one in five children with diabetes and nonautoimmune extra-pancreatic features have monogenic aetiology. 57th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE). Hormone Research in Paediatrics. Cilt 90. sf 213-213, 2018. (Yayına Ulaşmak İçin Tıklayınız)
18. Kirkgoz Tarik,Ozhan Bayram,Cetin Ozan,Kaygusuz Sare Betul,DEMİRCİOĞLU SERAP,BEREKET ABDULLAH,GÜRAN TÜLAY. Isolated Congenital Central Hypothyroidism due to a Novel Mutation in TSH Beta Subunit Gene.. Hormone Research in Paediatrics. 2018.
19. Kaygusuz Sare Betul,ATAY ZEYNEP,Kirkgoz Tarik,GÜRAN TÜLAY,BEREKET ABDULLAH,DEMİRCİOĞLU SERAP. An Unusual Cause of Short Stature. Hormone Research in Paediatrics. 2018.
20. Tarik Kirkgoz,Bas Serpil,Abali Zehra Yavas,DEMİRCİOĞLU SERAP,BEREKET ABDULLAH,GÜRAN TÜLAY. Delayed Diagnosis of a Patient with Antley-Bixler Syndrome.. Hormone Research in Paediatrics. 2018.
21. Ozbek Mehmet Nuri,Karasin Nezehat Dogan,DEMİRBİLEK HÜSEYİN,DEMİRAL MELİHA,BARAN RIZA TANER,GÜRAN TÜLAY. Presenting Features, Clinical Characteristics and Follow up of Familial Isolated Glucocorticoid Deficiency (FGD) due to Mutations in MC2R and MRAP Genes. Hormone Research in Pediatrics. 2018.
22. GÜRAN TÜLAY,Tezel Basak,Gurbuz Fatih,Eklioglu Beray Selver,Hatipoglu Nihal,Kara Cengiz,Sahin Nuran,Simsek Enver,Cizmecioglu Filiz Mine,Alev Ozon,Bas Firdevs,Aydin Murat,Ozdemir Gulsum,DARENDELİLER FATMA FEYZA. Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey:A Pilot Study with 38 935 Infants.. Hormone Research in Paediatrics. 2018.
23. Maharaj Avinaash,Bradshaw Teisha,Williams Jack,GÜRAN TÜLAY,Braslavsky Debora,Brugger Britta,Metherell Lou,Prasad Rathi. Sphingosine-1-Phosphate Lyase (SGPL1) Deficiency is Associated with Mitochondrial Dysfunction. Horm Res Paediatr. 2018.
24. KIRKGOZ TARIK,GÜRAN TÜLAY. Primary adrenal insufficiency in children: Diagnosis and management. Best Practice Research Clinical Endocrinology Metabolism. Cilt 32. sf 397-424, 2018. (Yayına Ulaşmak İçin Tıklayınız)
25. Baetens Dorien,GÜRAN TÜLAY,Mendonca Berenice B,Gomes Nathalia L,De Cauwer Lode,Peelman Frank,Verdin Hannah,Vuylsteke Marnik,Van der Linden,ATAY ZEYNEP,BEREKET ABDULLAH,de Krijger Ronald,Preter Katleen de,Domenice Sorahia,TURAN SERAP,Stoop Hans,Looijenga Leendert H,De Bosscher Karolien,Cools Martine,De Baere Elfride. Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex development. Genetics in Medicine. Cilt 20. sf 717-727, 2018. (Yayına Ulaşmak İçin Tıklayınız)
26. Chen Anlu,Tiosano Dov,GÜRAN TÜLAY,Baris Hagit N,BAYRAM YAVUZ,Mory Adi,Shapiro-Kulnane Laura,Craig A Hodges,Akdemir Zeynep C,DEMİRCİOĞLU SERAP,Jhangiani Shalini N,van den Akker,Hoppel Charles L,Salz Helen K,Lupski James R,Buchner David A. Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency. Human Molecular Genetics. Cilt 27. sf 1913-1926, 2018. (Yayına Ulaşmak İçin Tıklayınız)
27. POYRAZOĞLU ŞÜKRAN,DARENDELİLER FATMA FEYZA,AHMED SF,HUGHES I,Bryce J,Jiang J,Rodie M,Hiort O,Hannema SE,Bertelloni S,Lisa L,GÜRAN TÜLAY,Cools M,Desloovere A,Desloovere A,Claahsenvan der Grinten HL,Claahsenvan der Grinten HL,Nordenstrom A,Holterhus PM,Kohler B,Niedziela M,Nils K. Birth Weight in Different Etiologies of Disorders of Sex Development. The Journal of Clinical Endocrinology Metabolism. 2017. (Yayına Ulaşmak İçin Tıklayınız)
28. ŞIKLAR ZEYNEP,turan serap,BEREKET ABDULLAH,ABACI AYHAN,BAŞ FİRDEVS,DEMİR KORCAN,GÜRAN TÜLAY,akbarzade azad,BÖBER ECE,özbek MEHMET NURİ,KARA CENGİZ,POYRAZOĞLU ŞÜKRAN,AYDIN HASAN MURAT,KARDELEN ASLI,TARIM ÖMER FARUK,EREN ERDAL,HATİPOĞLU NİHAL,BÜYÜKİNAN MUAMMER,AKYÜREK NESİBE,ÇETİNKAYA SEMRA,BAYRAMOĞLU ELVAN,SELVER EKLİOĞLU BERAY,UÇAKTÜRK AHMET,ABALI SAYGIN,GÖKŞEN ŞİMŞEK RUHSAR DAMLA,kor yılmaz,ünal edip,ESEN İHSAN,YILDIRIM RUKEN,AKIN ONUR,ÇAYIR ATİLLA,DİLEK EMİNE,KİREL BİRGÜL,ANIK AHMET,ÇATLI GÖNÜL,BERBEROĞLU MERİH. nationwide hypophosphatemic rickets study57th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE). Hormone Research in Paediatrics. Cilt 90. sf 109-110, 2018. (Yayına Ulaşmak İçin Tıklayınız)
29. Savaş-Erdeve Şenay,ÇETİNKAYA SEMRA,Abalı Zehra Yavaş,POYRAZOĞLU ŞÜKRAN,BAŞ FİRDEVS,BERBEROĞLU MERİH,ŞIKLAR ZEYNEP,Korkmaz Özlem,Buluş Derya,Akbaş Emine Demet,GÜRAN TÜLAY,BÖBER ECE,Akın Onur,Yılmaz Gülay Can,AYCAN ZEHRA. Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height. Journal of Pediatric Endocrinology and Metabolism. Cilt 30. 2017. (Yayına Ulaşmak İçin Tıklayınız)
30. ABACI AYHAN,ÇATLI GÖNÜL,kırbıyık özgür,Şahin N M,Abalı Z Y,Ünal Edip,ŞIKLAR ZEYNEP,Mengen E,ÖZEN SAMİM,GÜRAN TÜLAY,KARA CENGİZ,Yıldız Metin,EREN ERDAL,Nalbantoğlu Ö,GÜVEN AYLA,Çayır Atilla,Akbaş E D,KÖR YILMAZ,çürek yusuf,AYCAN ZEHRA,BAŞ FİRDEVS,DARCAN ŞÜKRAN,BERBEROĞLU MERİH. Genotype–phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey. Journal of Endocrinological Investigation. 2018. (Yayına Ulaşmak İçin Tıklayınız)
31. SAVAŞ ERDEVE ŞENAY,ÇETİNKAYA SEMRA,YAVAŞ ABALI ZEHRA,poyrazoglu sükran,BAŞ FİRDEVS,BERBEROĞLU MERİH,ŞIKLAR ZEYNEP,KORKMAZ ÖZLEM,bulus derya,akbas emine demet,GÜRAN TÜLAY,BÖBER ECE,akın onur,yılmaz gülay can,AYCAN ZEHRA. Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height. Journal of Pediatric Endocrinology and Metabolism. Cilt 30. 2017. (Yayına Ulaşmak İçin Tıklayınız)
32. HALİLOĞLU BELMA,GÖKDEMİR YASEMİN,ATAY ZEYNEP,ABALI SAYGIN,GÜRAN TÜLAY,KARAKOÇ FAZİLET,ERSU REFİKA,KARADAĞ BÜLENT TANER,TURAN SERAP,BEREKET ABDULLAH. Hypoglycemia is common in children with cystic fibrosis and seen predominantly in females. PEDIATRIC DIABETES. Cilt 18. sf 607-613, 2017.
33. GÜRAN TÜLAY,BEREKET ABDULLAH. Oral bisphosphonate therapy for vitamin D intoxication of the infant. Pediatrics. Cilt 111. sf 899-901, 2003.
34. AKALIN FİGEN,TURAN SERAP,AYABAKAN CANAN,GÜRAN TÜLAY,YILMAZ YUKSEL. Increased QT dispersion in breath holding spells. Acta Pediatrica. Cilt 93. sf 770-774, 2004.
35. BIYIKLI NK,ALPAY HARİKA,GÜRAN TÜLAY. Hypercalciuria and recurrent urinary tract infections incidence and symptoms in children over 5 years of age. Pediatric Nephrology. Cilt 20. sf 1435-1438, 2005.
36. TURAN SERAP,GÜRAN TÜLAY,TOPCU B,AKCAY TEOMAN,BEREKET ABDULLAH. Severe diabetic ketoacidosis hyperventilation or relative hypoventilation. Pediatric Critical Care Medicine. Cilt 7. sf 291-, 2006.
37. GÜRAN TÜLAY,ERSU R,KARADAG BULENT,AKPINAR IN,DEMIREL GULDEREN,HEKIM NEZIH,DAGLI ELIF. Association between inflammatory markers in induced sputum and clinical characteristics in children with non cystic fibrosis bronchiectasis. Pediatric Pulmonology. Cilt 42. sf 362-369, 2007.
38. TURAN SERAP,BEREKET ABDULLAH,GÜRAN TÜLAY,AKCAY TEOMAN,PapariZareei M,AUCHUS R. Puberty in a case with novel 17 hydroxylase mutation and the putative role of estrogen in development of pubic hair. European Journal of Endocrinology. Cilt 160. sf 325-330, 2008. (Yayına Ulaşmak İçin Tıklayınız)
39. GÜRAN TÜLAY,TURAN SERAP,ERSU REFIKA,KARADAG BULENT, KARAKOC FAZILET,BEREKET ABDULLAH,DAGLI ELIF. Bone mineral density in children with non cystic fibrosis bronchiectasis. Respiration. Cilt 75. sf 432-436, 2008.
40. AKCAY TEOMAN,GÜRAN TÜLAY,TURAN SERAP,BEREKET ABDULLAH. Alendronate treatment in children with osteogenesis imperfecta. Indian Pediatrics. Cilt 45. sf 105-109, 2008.
41. GÜRAN TÜLAY,ERSU REFIKA,KARADAG BULENT,KARAKOC FAZILET,DEMIREL GY,HEKIM NEZIH,DAGLI ELIF. Withdrawal of inhaled steroids in children with non cystic fibrosis bronchiectasis. Journal of Clinical Pharmacy and Therapeutics. Cilt 33. sf 603-611, 2008. (Yayına Ulaşmak İçin Tıklayınız)
42. POYRAZOGLU S,SAKA NURCIN,BAS FIRDEVS,ISGUVEN PINAR,DOGU A,DARENDELİLER FATMA FEYZA,TURAN SERAP,SARIKAYA SEVIL,ADAL SERVET ERDAL,CIZMECIOGLU FILIZ,SAGLAM HALIL,ERCAN OYA,MEMIOGLU NIHAL,GUNOZ HULYA,BEREKET ABDULLAH,BUNDAK RUVEYDE,YILDIZ METIN,GÜRAN TÜLAY,AKCAY TEOMAN,AKIN LEYLA,HATUN SUKRU. Evaluation of diagnosis and treatment results in children with Graves disease with emphasis on the pubertal status of patients. Journal of Pediatric Endocrinology and Metabolism. Cilt 21. sf 745-751, 2008.
43. GÜRAN TÜLAY,TURAN SERAP,AKCAY TEOMAN,BEREKET ABDULLAH. Significance of acanthosis nigricans in childhood obesity. Journal of Paediatrics and Child Health. Cilt 44. sf 338-341, 2008. (Yayına Ulaşmak İçin Tıklayınız)
44. GÜRAN TÜLAY,TURAN SERAP,BEREKET ABDULLAH,DARENDELİLER FATMA FEYZA,AKCAY TEOMAN,UNLUGUZEL G,BAS FIRDEVS,GUNOZ HULYA,SAKA NURCIN,BUNDAK RUVEYDE,ISGUVEN PINAR,YILDIZ METIN,ADAL ERDAL,SARIKAYA SEVIL,AKIN LEYLA,MEMIOGLU NIHAL,ONAL HASAN,ERCAN OYA,HAKLAR GONCAGUL. The role of leptin soluble leptin receptor resistin and insulin secretory dynamics in the pathogenesis of hypothalamic obesity in children. European Journal of Pediatrics. Cilt 168. sf 1043-1048, 2009. (Yayına Ulaşmak İçin Tıklayınız)
45. Bottomley WE,SOOS MA,ADAMS C,GÜRAN TÜLAY,Howlett TA,Mackie A,Miell J,Monson JP,Temple J,TEMPLE R,TenenbaumRakover Y,Tymms J,Savage DB,Semple RK,ORahilly S,Barroso I. IRS2 variants and syndromes of severe insulin resistance. Diabetologia. Cilt 52. sf 1208-1211, 2009. (Yayına Ulaşmak İçin Tıklayınız)
46. GÜRAN TÜLAY,Tolhurst Gwen,BEREKET ABDULLAH,Rocha Nuno,Porter Keith,TURAN SERAP,Gribble Fiona M,Kotan L Damla,Akcay Teoman,Atay Zeynep,Canan Husniye,Serin Ayse,O'Rahilly Stephen,Reimann Frank,Semple Robert K,Topaloglu A Kemal. Hypogonadotropic Hypogonadism due to a Novel Missense Mutation in the First Extracellular Loop of the Neurokinin B Receptor. The Journal of Clinical Endocrinology & Metabolism. Cilt 94. sf 3633-3639, 2009. (Yayına Ulaşmak İçin Tıklayınız)
47. GÜRAN TÜLAY,TURAN SERAP,OZKAN B,BERRAK SG,CANPOLAT CENGİZ,DAGLI T,EREN FS,BEREKET ABDULLAH. Cushing s syndrome due to a non adrenal ectopic adrenocorticotropin secreting Ewing s sarcoma in a child. Journal of Pediatric Endocrinology and Metabolism. Cilt 22. sf 363-368, 2009.
48. RubioCabezas O,Patch AM,Minton JA,Flanagan SE,Edghill EL,Hussain K,Balafrej A,A Deeb,Buchanan CR,Jefferson IG,Mutair A,GÜRAN TÜLAY,Hattersley AT,ELLARD S. Wolcott Rallison Syndrome Is the Most Common Genetic Cause of Permanent Neonatal Diabetes in Consanguineous Families. The Journal of Clinical Endocrinology & Metabolism. Cilt 94. sf 4162-4170, 2009. (Yayına Ulaşmak İçin Tıklayınız)
49. GÜRAN TÜLAY,BIRCAN RIFAT,TURAN SERAP,BEREKET ABDULLAH. Alopecia association with resistance to thyroid hormones. Journal of Pediatric Endocrinology and Metabolism. Cilt 22. sf 1075-1081, 2009.
50. GÜRAN TÜLAY,TURAN SERAP,BIRCAN RIFAT,BEREKET ABDULLAH. 9 years follow up of a patient with pituitary form of resistance to thyroid hormones PRTH comparison of two treatment periods of D thyroxine and triiodothyroacetic acid TRIAC. Journal of Pediatric Endocrinology and Metabolism. Cilt 22. sf 971-978, 2009.
51. GÜRAN TÜLAY,TURAN SERAP,AKCAY T,DEGIRMENCI F,AVCI O,A Asan,Erdil E,A Majid,BEREKET ABDULLAH. Content analysis of food advertising in Turkish television. Journal of Paediatrics and Child Health. Cilt 46. sf 427-430, 2010. (Yayına Ulaşmak İçin Tıklayınız)
52. AKCAY T,TURAN SERAP,GÜRAN TÜLAY,UNLUGUZEL G,HAKLAR GONCAGUL,BEREKET ABDULLAH. T4 plus T3 Treatment in Children with Hypothyroidism and Inappropriately Elevated Thyroid Stimulating Hormone despite Euthyroidism on T4 Treatment. Hormone Research in Paediatrics. Cilt 73. sf 108-114, 2010. (Yayına Ulaşmak İçin Tıklayınız)
53. TURAN SERAP,C AYDIN,BEREKET ABDULLAH,AKCAY T,GÜRAN TÜLAY,YARALIOGLUU BA,BASTEPE M,Jüppner H. Identification of a novel dentin matrix protein 1 DMP 1 mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia. Bone. Cilt 46. sf 402-409, 2010. (Yayına Ulaşmak İçin Tıklayınız)
54. GÜRAN TÜLAY,DEGIRMENCI S,BULUT IK,SAY A,Riepe FG,GURAN O. Critical Points in the Management of Pseudohypoaldosteronism Type 1 Case Report. journal of Clinical Research in Pediatric Endocrinology. Cilt 3. sf 98-100, 2011. (Yayına Ulaşmak İçin Tıklayınız)
55. TURAN SERAP,OZDEMIR NIHAL,GÜRAN TÜLAY,AKALIN FİGEN,AKCAY TEOMAN,AYABAKAN CANAN,YILMAZ YUKSEL,BEREKET ABDULLAH. Constitutional Growth Delay Pattern of Growth in Velo Cardio Facial Syndrome Longitudinal follow up and final height of two cases. Journal of Clinical Research in Pediatric Endocrinology. Cilt 1. sf 43-48, 2011. (Yayına Ulaşmak İçin Tıklayınız)
56. Schlingmann KP,Kaufmann M,Weber S,Irwin A,GOOD C,JOHN U,Misselwitz J,Klaus G,KLAUS G,KuwertzBröking E,Fehrenbach H,Wingen AM,GÜRAN TÜLAY,Hoenderop JG,Bindels RJ,Prosser DE,Jones G,KONRAD M. Mutations in CYP24A1 and idiopathic infantile hypercalcemia. New England Journal of Medicine. Cilt 365. sf 410-421, 2011. (Yayına Ulaşmak İçin Tıklayınız)
57. KarakocAydiner ELIF,TURAN SERAP,AKPINAR IN,DEDE FUAT,ISGUVEN PINAR,ADAL ERDAL,GÜRAN TÜLAY,AKCAY TEOMAN,BEREKET ABDULLAH. Pitfalls in the diagnosis of thyroid dysgenesis by thyroid ultrasonography and scintigraphy. European Journal of Endocrinology. Cilt 166. sf 43-48, 2011. (Yayına Ulaşmak İçin Tıklayınız)
58. ATAY Z,TURAN SERAP,GÜRAN TÜLAY,FURMAN ANDRZEJ,BEREKET ABDULLAH. Puberty and Influencing Factors in Schoolgirls Living in Istanbul End of the Secular Trend. PEDIATRICS. Cilt 128. sf 40-45, 2011. (Yayına Ulaşmak İçin Tıklayınız)
59. GÜRAN TÜLAY,ARMAN A,AKCAY T,KAYAN E,ATAY Z,TURAN S,BEREKET ABDULLAH. Cognitive and psychosocial development in children with familial hypomagnesaemia. Magnesium Research. Cilt 24. sf 7-12, 2011.
60. AKESEN E,TURAN SERAP,GÜRAN TÜLAY,ATAY Z,SAVE DİLŞAD,BEREKET ABDULLAH. Prevalence of type 1 diabetes mellitus in 6 18 yr old school children living in Istanbul Turkey. Pediatric Diabetes. 2011. (Yayına Ulaşmak İçin Tıklayınız)
61. GÜRAN TÜLAY,BEREKET ABDULLAH. International epidemic of childhood obesity and television viewing. Minerva Pediatrica. Cilt 63. sf 483-490, 2011.
62. GÜRAN TÜLAY,EKINCI G,ATAY Z,TURAN SERAP,AKCAY T,BEREKET ABDULLAH. Radiologic and hormonal evaluation of pituitary abnormalities in patients with Bardet Biedl syndrome. Clinical Dysmorphology. Cilt 20. sf 26-31, 2011. (Yayına Ulaşmak İçin Tıklayınız)
63. TURAN SERAP,GÜRAN TÜLAY,TOPCU B,GOKCE I,OMAR A,ATAY Z,AKCAY T,BEREKET ABDULLAH. Serum Alkaline Phosphatase Levels in Healthy Children and Evaluation of Alkaline Phosphatase z scores in Different Types of Rickets. Journal of Clinical Research in Pediatric Endocrinology. Cilt 3. sf 7-11, 2011. (Yayına Ulaşmak İçin Tıklayınız)
64. GÜRAN TÜLAY,KARASU GT,DEGIRMENCI S,SAY A,GURAN O,PAKETCI AT,KORNAK UWE. A Rare Cause of a Relatively Common Neonatal Emergency. Pediatric Hematology-Oncology. Cilt 29. sf 365-367, 2012. (Yayına Ulaşmak İçin Tıklayınız)
65. GÜRAN TÜLAY,Yeşil Gözde,Güran Ömer,Cesur Suna,Bosnalı Oktav,Celayir Ayşenur,Topçuoğlu Sevilay,BEREKET ABDULLAH. A Giant Ovarian Cyst in a Neonate with Classical 21 Hydroxylase Deficiency with Very High Testosterone Levels Demonstrating a High Dose Hook Effect. Journal of Clinical Research in Pediatric Endocrinology. Cilt 4. sf 151-153, 2012. (Yayına Ulaşmak İçin Tıklayınız)
66. TURAN SERAP,Hughes Claire,Atay Zeynep,GÜRAN TÜLAY,Haliloglu Belma,Clark Adrian J,BEREKET ABDULLAH,Metherell Louise A. An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R T152K and MC1R R160W. The Journal of Clinical Endocrinology & Metabolism. Cilt 97. sf 771-774, 2012. (Yayına Ulaşmak İçin Tıklayınız)
67. Bonnard Carine,Strobl Anna C,Shboul Mohammad,Lee Hane,Barry Merriman,Nelson Stanley F,Ababneh Osama H,UZ ELİF,GÜRAN TÜLAY,Kayserili Hülya,Hamamy Hanan,Reversade Bruno. Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1. Nature Genetics. Cilt 44. sf 709-713, 2012. (Yayına Ulaşmak İçin Tıklayınız)
68. GÜRAN TÜLAY,AKCAY T,BEREKET ABDULLAH,ATAY Z,TURAN SERAP,Haisch L,KONRAD M,Schlingmann KP. Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia novel mutations in TRPM6 and CLDN16 genes. Nephrology Dialysis Transplantation. Cilt 27. sf 667-673, 2012. (Yayına Ulaşmak İçin Tıklayınız)
69. SEZER RG,GÜRAN TÜLAY,PAKETCI C,SEREN LP,BOZAYKUT A,BEREKET ABDULLAH. Comparison of oral alendronate versus prednisolone in treatment of infants with vitamin D intoxication. Acta Paediatrica. Cilt 101. sf 122-125, 2012. (Yayına Ulaşmak İçin Tıklayınız)
70. ATAY Z,TURAN SERAP,GÜRAN TÜLAY,FURMAN ANDRZEJ,BEREKET ABDULLAH. The prevalence and risk factors of premature thelarche and pubarche in 4 to 8 year old girls. Acta Paediatrica. Cilt 101. sf 71-75, 2012. (Yayına Ulaşmak İçin Tıklayınız)
71. Welzel M,AKIN LEYLA,Buscher A,GÜRAN TÜLAY,Hauffa B P,Hogler W,Leonards J,KARGES B,KENTRUP H,KİREL BİRGÜL,SENSES EE,TEKİN NESLİHAN,Holterhus PM,Riepe F. Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1. European Journal of Endocrinology. Cilt 168. sf 707-715, 2013. (Yayına Ulaşmak İçin Tıklayınız)
72. Sezer Rabia Gönül,Aydemir Gökhan,Akcan Abdullah Barıs,Bayoglu Duygu Somen,GÜRAN TÜLAY,Bozaykut Abdulkadir. Effect of Breastfeeding on Serum Zinc Levels and Growth in Healthy Infants. Breastfeeding Medicine. Cilt 8. sf 159-163, 2013. (Yayına Ulaşmak İçin Tıklayınız)
73. Haliloglu Belma,GÜRAN TÜLAY,Atay Zeynep,Abali Saygın,Mornet Etienne,BEREKET ABDULLAH,TURAN SERAP. Infantile loss of teeth odontohypophosphatasia or childhood hypophosphatasia. European Journal of Pediatrics. Cilt 172. sf 851-853, 2013. (Yayına Ulaşmak İçin Tıklayınız)
74. Cox Kathryn,Bryce Jillian,Jiang Jipu,Rodie Martina,Sinnott Richard,Alkhawari Mona,Arlt Wiebke,Audi Laura,Balsamo Antonio,Bertelloni Silvano,Cools Martine,DARENDELİLER FATMA FEYZA,Drop Stenvert,Ellaithi Mona,GÜRAN TÜLAY,Hiort Olaf,Holterhus Paul-Martin,Hughes Ieuan,Krone Nils,Lisa Lidka,Morel Yves,Soder Olle,Wieacker Peter,Ahmed S Faisal. Novel Associations in Disorders of Sex Development Findings From the I DSD Registry. The Journal of Clinical Endocrinology & Metabolism. Cilt 99. sf 348-355, 2014. (Yayına Ulaşmak İçin Tıklayınız)
75. Akcay T,Fernandez-Cancio M,TURAN S,GÜRAN TÜLAY,Audi L,BEREKET ABDULLAH. AR and SRD5A2 gene mutations in a series of 51 Turkish 46 XY DSD children with a clinical diagnosis of androgen insensitivity. Andrology. Cilt 2. sf 572-578, 2014. (Yayına Ulaşmak İçin Tıklayınız)
76. Kühnen Peter,Turan Serap,Fröhler Sebastian,GÜRAN TÜLAY,Abali Saygin,Biebermann Heike,Bereket Abdullah,Grüters Annette,Chen Wei,Krude Heiko. Identification of PENDRIN SLC26A4 Mutations in Patients With Congenital Hypothyroidism and Apparent Thyroid Dysgenesis. The Journal of Clinical Endocrinology & Metabolism. Cilt 99. sf 169-176, 2014. (Yayına Ulaşmak İçin Tıklayınız)
77. Yeşil Gözde,Lebre Anne Sophie,Santos Sofia Dos,Güran Ömer,Özahi Ilke Ipek,Özahi Ilke Ipek,GÜRAN TÜLAY. Stuve Wiedemann syndrome Is it underrecognized. American Journal of Medical Genetics Part A. Cilt 164. sf 2200-2205, 2014. (Yayına Ulaşmak İçin Tıklayınız)
78. ARMAN AHMET,BEREKET ABDULLAH,Coker Ajda,ŞİMŞEK KİPER PELİN ÖZLEM,GÜRAN TÜLAY,ÖZKAN BEHZAT,Atay Zeynep,Akçay Teoman,Haliloglu Belma,Boduroglu Koray,ALANAY YASEMİN,TURAN SERAP. Cathepsin K analysis in a pycnodysostosis cohort demographic genotypic and phenotypic features. Orphanet Journal of Rare Diseases. Cilt 9. sf 60-, 2014. (Yayına Ulaşmak İçin Tıklayınız)
79. Kolesinska Z,Ahmed S F,Niedziela M,Bryce J,Molinska-Glura M,Rodie M,Jiang J,Sinnott R O,Hughes I A,FURMAN ANDRZEJ,Hiort O,van der Zwan,Cools M,GÜRAN TÜLAY,P-M Holterhus,Bertelloni S,L Lisa,Arlt W,Krone N,Ellaithi M,Balsamo A,Mazen I,Nordenstrom A,Lachlan K,Alkhawari M,Chatelain P,Weintrob N. Changes Over Time in Sex Assignment for Disorders of Sex Development. PEDIATRICS. Cilt 134. sf 710-715, 2014. (Yayına Ulaşmak İçin Tıklayınız)
80. Kirac Deniz,Guney Ahmet Ilter,Akcay Teoman,GÜRAN TÜLAY,ULUCAN KORKUT,TURAN SERAP,Ergec Deniz,Koc Gulsah,EREN FATİH,Kaspar Elif Cigdem,Bereket Abdullah. The Frequency and the Effects of 21 Hydroxylase Gene Defects in Congenital Adrenal Hyperplasia Patients. Annals of Human Genetics. Cilt 78. sf 399-409, 2014. (Yayına Ulaşmak İçin Tıklayınız)
81. Simpkin Arabella,Cochran Elaine,Cameron Fergus,Dattani Mehul,de Bock Martin,Dunger David B,Forsander Gun,GÜRAN TÜLAY,Harris Julie,Iona Isaac,Hussain Khalid,Kleta Robert,Peters Catherine,Tasic Velibor,Williams Rachel,Yap Kok Peng,O''Rahilly Stephan,Gorden Philipp,Robert K Semple,Detlef Bockenhauer. Insulin Receptor and the Kidney Nephrocalcinosis in Patients with Recessive INSR Mutations. Nephron Physiology. Cilt 128. sf 55-61, 2014. (Yayına Ulaşmak İçin Tıklayınız)
82. GÜRAN TÜLAY,Guran Omer,Paketci Cem,Kipoglu Osman,Firat Irfan,TURAN SERAP,Atay Zeynep,Haliloglu Belma,BEREKET ABDULLAH. Effects of leukemia inhibitory receptor gene mutations on human hypothalamo pituitary adrenal function. Pituitary. Cilt 18. sf 456-460, 2015. (Yayına Ulaşmak İçin Tıklayınız)
83. GÜRAN TÜLAY,Irfan Firat,YILDIZ FEYZA,Kaplan Bulut Ipek,Dogru Mahmut,BEREKET ABDULLAH. Reference values for serum dehydroepiandrosterone sulphate in healthy children and adolescents with emphasis on the age of adrenarche and pubarche. Clinical Endocrinology. Cilt 82. sf 712-718, 2015. (Yayına Ulaşmak İçin Tıklayınız)
84. GÜRAN TÜLAY. Response to the Letter to the Editor Regarding the Article Reference values for serum dehydroepiandrosterone sulphate in healthy children and adolescents with emphasis on the age of adrenarche and pubarche. Clinical Endocrinology. Cilt 82. sf 913-914, 2015. (Yayına Ulaşmak İçin Tıklayınız)
85. BAYRAM YAVUZ,Gulsuner Suleyman,GÜRAN TÜLAY,Abaci Ayhan,Yesil Gozde,Gulsuner Hilal Unal,Atay Zeynep,Pierce Sarah B,Gambin Tomasz,Lee Ming,TURAN SERAP,Bober Ece,Atik Mehmed M,Walsh Tom,Karaca Ender,Pehlivan Davut,Jhangiani Shalini N,Muzny Donna,BEREKET ABDULLAH,Buyukgebiz Atilla,Boerwinkle Eric,Gibbs Richard A,King Mary-Claire,Lupski James R. Homozygous loss of function mutations in SOHLH1 in patients with non syndromic hypergonadotropic hypogonadism. The Journal of Clinical Endocrinology & Metabolism. Cilt 100. sf 808-814, 2015. (Yayına Ulaşmak İçin Tıklayınız)
86. Bas Serpil,GÜRAN TÜLAY,Atay Zeynep,Haliloglu Belma,Abali Saygin,TURAN SERAP,BEREKET ABDULLAH. Premature Pubarche Hyperinsulinemia and Hypothyroxinemia Novel Manifestations of Congenital Portosystemic Shunts Abernethy Malformation in Children. Hormone Research in Paediatrics. Cilt 83. sf 282-287, 2015. (Yayına Ulaşmak İçin Tıklayınız)
87. Doga Turkkahraman,GÜRAN TÜLAY,Ivison Hannah,Griffin Aliesha,Vijzelaar Raymon,Krone Nils. Identification of a novel large CYP17A1 deletion by MLPA analysis in a family with classic 17 hydroxylase deficiency. Sexual Development. Cilt 9. sf 91-97, 2015. (Yayına Ulaşmak İçin Tıklayınız)
88. ABALI SAYGIN,TURAN SERAP,Atay Zeynep,GÜRAN TÜLAY,Haliloğlu Belma,BEREKET ABDULLAH. Higher insulin detemir doses are required for the similar glycemic control comparison of insulin detemir and glargine in children with type 1 diabetes mellitus. Pediatric Diabetes. Cilt 16. sf 361-366, 2015. (Yayına Ulaşmak İçin Tıklayınız)
89. Özbörü Aşkan Öykü,Bozaykut Abdülkadir,Sezer Rabia Gönül,GÜRAN TÜLAY,BEREKET ABDULLAH. Effect of Maternal Factors and Fetomaternal Glucose Homeostasis on Birth Weight and Postnatal Growth. Journal of Clinical Research in Pediatric Endocrinology. Cilt 7. sf 168-174, 2015. (Yayına Ulaşmak İçin Tıklayınız)
90. ATAY ZZ,YESILKAYA EE,SAVAS ERDEVE SS,TURAN SERAP,AKIN LEYLA,EREN ERDAL,DOGER ESRA,AYCAN ZEHRA,ABALI ZEHRA YAVAS,AKINCI AA,SIKLAR ZZ,OZEN SS,KARA CC,MM Tayfun,Sari EE,Tutunculer FF,Seymen Karabulut GG,Karaguzel GG,Cetinkaya SS,Saglam HH,BİDECİ AYSUN,Kurtoglu SS,GÜRAN TÜLAY,BEREKET ABDULLAH. The Etiology and Clinical Features of Non CAH Gonadotropin Independent Precocious Puberty A Multicenter Study. The Journal of Clinical Endocrinology & Metabolism. Cilt 101. sf 1980-1988, 2016. (Yayına Ulaşmak İçin Tıklayınız)
91. Haliloglu B,Atay Z,GÜRAN TÜLAY,ABALI SAYGIN,Bas S,S Turan,TURAN SERAP,BEREKET ABDULLAH. Risk factors for mortality caused by hypothalamic obesity in children with hypothalamic tumours. Pediatric Obesity. Cilt 11. sf 383-388, 2016. (Yayına Ulaşmak İçin Tıklayınız)
92. Dikoglu Esra,Alfaiz Ali,Gorna Maria,Bertola Deborah,Chae Jong Hee,Cho Tae-Joon,Derbent Murat,ALANAY YASEMİN,GÜRAN TÜLAY,Kim Ok-Hwa,Llerenar Jr Juan,Yamamoto Guillerme,Superti-Furga Giulio,Reymond Alexandre,Xenarios Ioannis,Stevenson Brian,Campos-Xavier Belinda,Bonafé Luisa,Superti-Furga Andrea,Unger Sheila. Mutations in LONP1 a mitochondrial matrix protease cause CODAS syndrome. American Journal of Medical Genetics Part A. Cilt 167. sf 1501-1509, 2015. (Yayına Ulaşmak İçin Tıklayınız)
93. Karaca Ender,Harel Tamar,Pehlivan Davut,Jhangiani Shalini N,Gambin Tomasz,Coban Akdemir Zeynep,Gonzaga-Jauregui Claudia,Erdin Serkan,Bayram Yavuz,Campbell Ian M,Hunter Jill V,Atik Mehmed M,Van Esch Hilde,Yuan Bo,Wiszniewski Wojciech,Isikay Sedat,Yesil Gozde,Yuregir Ozge O,Tug Bozdogan Sevcan,Aslan Huseyin,Aydin Hatip,Tos Tulay,Aksoy Ayse,De Vivo Darryl,Jain Preti,Geckinli B Bilge,Sezer Ozlem,Gul Davut,Durmaz Burak,Cogulu Ozgur,Ozkinay Ferda,Vehap Topcu,Sukru Candan,Alper Han Cebi,Mevlit Ikbal,Gulec Elif Yilmaz,Yilmaz Gulec Elif,Alper Gezdirici,Gezdirici Alper,Koparir Erkan,Ekici Fatma,Coskun Salih,Cicek Salih,Karaer Kadri,Koparir Asuman,Duz Mehmet Bugrahan,Kirat Emre,Fenercioglu Elif,Ulucan Hakan,Seven Mehmet,GÜRAN TÜLAY,Elcioglu Nursel,Yildirim Mahmut Selman,Aktas Dilek,Alikaşifoğlu Mehmet,Ture Mehmet,Yakut Tahsin,Overton John D,Yuksel Adnan,Ozen Mustafa,Muzny Donna M,Adams David R,Boerwinkle Eric,Chung Wendy K,Gibbs Richard A,Lupski James R. Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease. Neuron. Cilt 88. sf 499-513, 2015. (Yayına Ulaşmak İçin Tıklayınız)
94. GÜRAN TÜLAY,Buonocore Federica,Saka Nurcin,Ozbek Mehmet Nuri,AYCAN ZEHRA,BEREKET ABDULLAH,BAS FIRDEVS,Darcan Sukran,BİDECİ AYSUN,Ayla Guven,Demir Korcan,Akinci Aysehan,Buyukinan Muammer,Aydin Banu Kucukemre,TURAN SERAP,Sebahat Yilmaz Agladioglu,Agladioglu Sebahat Yilmaz,Agladioglu Sebahat Yilmaz,Atay Zeynep,Abali Zehra Yavas,Tarim Omer,Catli Gonul,Bilgin Yuksel,Akcay Teoman,Yildiz Metin,Ozen Samim,Doger Esra,Demirbilek Huseyin,Ucar Ahmet,Isik Emregul,Ozhan Bayram,Bolu Semih,Bolu Semih,Ozgen Ilker Tolga,Suntharalingham Jenifer P,Achermann John C. Rare Causes of Primary Adrenal Insufficiency Genetic and Clinical Characterization of a Large Nationwide Cohort. The Journal of Clinical Endocrinology & Metabolism. Cilt 101. sf 284-292, 2016. (Yayına Ulaşmak İçin Tıklayınız)
95. Haliloglu BB,Hysenaj GG,Atay ZZ,GÜRAN TÜLAY,ABALI SAYGIN,TURAN SERAP,BEREKET ABDULLAH. GCK Gene Mutations are a Common Cause of Childhood Onset MODY Maturity Onset Diabetes Of The Young in Turkey. Clinical Endocrinology. Cilt 85. sf 393-399, 2016. (Yayına Ulaşmak İçin Tıklayınız)
96. LucasHerald AA,Bertelloni SS,Juul AA,Bryce JJ,Jiang JJ,Rodie MM,Sinnott RR,Boroujerdi MM,LindhartJohansen MM,Hiort OO,Holterhus PM,Cools MM,Desloovere AA,GuaragnaFilho GG,GuerraJunior GG,Weintrob NN,Hannema SS,Drop SS,GÜRAN TÜLAY,DARENDELİLER FATMA FEYZA,Nordenstrom AA,Hughes IA,Acerini CC,TadokoroCuccaro RR,SF Ahmed. The Long Term Outcome of Boys With Partial Androgen Insensitivity Syndrome and a Mutation in the Androgen Receptor Gene. The Journal of Clinical Endocrinology & Metabolism. Cilt 101. sf 3959-3967, 2016. (Yayına Ulaşmak İçin Tıklayınız)
DİĞER DERGİLERDE YAYIMLANAN MAKALELER
1. Weger Meltem,Weger Benjamin D,Görling Benjamin,Poschet Gernot,Yildiz Melek,Hell Rüdiger,Luy Burkhard,Akcay Teoman,GÜRAN TÜLAY,Dickmeis Thomas,Müller Ferenc,Krone Nils. Glucocorticoid deficiency causes transcriptional and post-transcriptional reprogramming of glutamine metabolism. EBioMedicine. Cilt 36. sf 376-389, 2018. (Yayına Ulaşmak İçin Tıklayınız)
2. Maharaj Avinaash,Buonocore Federica,Meimaridou Eirini,Ruiz-Babot Gerard,Guasti Leonardo,Peng Hwei-Ming,Capper Cameron P,Burgos-Tirado Neikelyn,Prasad Rathi,Hughes Claire R,Maudhoo Ashwini,Crowne Elizabeth,Cheetham Timothy D,Brain Caroline E,Suntharalingham Jenifer P,Striglioni Niccolò,Yuksel Bilgin,Gurbuz Fatih,Gupta Sangay,Lindsay Robert,Couch Robert,Spoudeas Helen A,GÜRAN TÜLAY,Johnson Stephanie,Conwell Louise S,Fowler Dallas J,McInerney-Leo Aideen M,Drui Delphine,Cariou Bertrand,Lopez-Siguero Juan P,Harris Mark,Duncan Emma L,Hindmarsh Peter C,Auchus Richard J,Donaldson Malcolm D,Achermann John C,Metherell Louise A. title Predicted Benign and Synonymous Variants in iCYP11A1/i Cause Primary Adrenal Insufficiency Through Missplicing/title. Journal of the Endocrine Society. Cilt 3. sf 201-221, 2018. (Yayına Ulaşmak İçin Tıklayınız)
ULUSAL
SCI, SSCI, AHCI İNDEKSLERİNE GİREN DERGİLERDE YAYINLANAN MAKALELER
1. KAVURT Sumru,ÖZBEK Mehmet Nuri,GÜRAN TÜLAY. Familial Glucocorticoid Defificiency in a Newborn Caused by a Mutation in Melanocortin 2 Receptor: Case Report. Turkiye Klinikleri Journal of Case Reports. Cilt 25. sf 95-98, 2017. (Yayına Ulaşmak İçin Tıklayınız)
DİĞER DERGİLERDE YAYIMLANAN MAKALELER
1. YİĞİT ŞULE,KAYNAK TÜRKMEN MÜNEVVER,TUNCER OĞUZ,TAŞKIN ERDAL,GÜRAN TÜLAY,ABACI AYHAN,ÇATLI GÖNÜL,TARIM ÖMER FARUK. Neonatal Adrenal Yetmezlik: Türk Neonatoloji ve Çocuk Endokrinoloji ve Diyabet Dernekleri Uzlaşı raporu. Türk Pediatri Arşivi. sf 239-243, 2018.
KİTAPLAR
ULUSLARARASI
BİLİMSEL KİTAP
KİTAP BÖLÜMÜ
1. Baranowski EE,GÜRAN TÜLAY,Krone NP, Neuroendocrine Disorders in Children, 2016. (Yayına Ulaşmak İçin Tıklayınız)
DERS KİTABI
KİTAP BÖLÜMÜ
2. GÜRLER ESRA BİHTER, DİŞHEKİMLİĞİ BAKIŞ AÇISIYLA SİSTEMİK HASTALIKLAR, 2017.
ULUSAL
BİLİMSEL KİTAP
KİTAP BÖLÜMÜ
3. GÜRAN TÜLAY, Yogun Bakim Hemsireligi: Esaslar ve Uygulamalar, 2018.
4. NORGAZ NİYAZİ TUĞRUL,bahar özcabı,dursun fatma,GÜRAN TÜLAY,erdem ela,derya kocakaya,refika hamutçu,mehmet gökan gönenli,ÇETİNER MUSTAFA,miray cimşit,can ege yalçın,aslıhan taraktaş,KENDİRLİ MUSTAFA TANSEL,güney duman deniz,GÜNDÜZ FEYZA,barutçu dilek,GÜLÇEBİ İDRİZ OĞLU MEDİNE,GÖREN MEHMET ZAFER,ARIKAN İZZET HAKKI, Diş hekimliği bakış açısıyla sistemik hastalıklar, 2017.
5. BERBEROĞLU MERİH,DARCAN ŞÜKRAN,YÜKSEL BİLGİN,AYDIN HASAN MURAT,ORBAK ZERRİN,EVLİYAOĞLU SAADET OLCAY,ŞIKLAR ZEYNEP,ABACI AYHAN,GÜRAN TÜLAY,SAVAŞ ERDEVE ŞENAY,Kırmızıbekmez Heves,Hacıhamdioğlu Bülent,Akın Leyla,ÇATLI GÖNÜL, Çocuk Endokrinolojisinde Uzlaşı, 2017.
DERS KİTABI
KİTAP BÖLÜMÜ
6. OZCABI BB,DURSUN FF,GÜRAN TÜLAY, Dis hekimligi bakis acisi ile sistemik hastaliklar, 2016.
7. GÜRAN TÜLAY, Yurdakok Pediatri, 2016.
EDİTÖRLÜKLER
Henüz içerik girilmemiş.
BİLDİRİLER
ULUSLARARASI
1. ŞIKLAR ZEYNEP,turan serap,BEREKET ABDULLAH,ABACI AYHAN,BAŞ FİRDEVS,DEMİR KORCAN,GÜRAN TÜLAY,akberzade azad,BÖBER ECE,özbek mehmet nuri,KARA CENGİZ,POYRAZOĞLU ŞÜKRAN,AYDIN HASAN MURAT,kardelen aslı,TARIM ÖMER FARUK,EREN ERDAL,HATİPOĞLU NİHAL,büyükinan muammer,akyürek nesibe,ÇETİNKAYA SEMRA,bayramoğlu elvan,SELVER EKLİOĞLU BERAY,UÇAKTÜRK AHMET,ABALI SAYGIN,GÖKŞEN ŞİMŞEK RUHSAR DAMLA,kor yılmaz,ünal edip,ESEN İHSAN,YILDIRIM RUKEN,AKIN ONUR,ÇAYIR ATİLLA,DİLEK EMİNE,KİREL BİRGÜL,ANIK AHMET,ÇATLI GÖNÜL,BERBEROĞLU MERİH, "Nationwide Hypophosphatemic Rickets Study", 57th Annual meeting of ESPE, Atina, 2018.
2. kaygusuz sare betul,yesil gozde,Kırkgoz Tarık,DEMİRCİOĞLU SERAP,BEREKET ABDULLAH,GÜRAN TÜLAY, "An 18 Month Old Boy with Hypoglycemic Convulsion and Obesity Due to POMC Deficiency", The 57th Annual ESPE Meeting, 2018.
3. Patel Kashyap A,Colclough Kevin,Ozbek Mehmet Nuri,Yildiz Melek,GÜRAN TÜLAY,Kocyigit Cemil,Sezer Acar,Siklar Zeynep,Atar Muge,Johnson Matt B,Cizmecioglu Filiz Mine,Merih Berberoglu,DEMİR KORCAN,DEMİRBİLEK HÜSEYİN,Hattersley Andrew T, ". Comprehensive Genetic Testing Shows One in Five Children with Diabetes and Non-Autoimmune Extra-Pancreatic Features Have Monogenic Aetiology.", The 57th Annual ESPE Meeting, 2018.
4. yildiz melek,bas firdevs,turan serap,isik emregul,KARA CENGİZ,barnard lisa,DARENDELİLER FATMA FEYZA,baris tuba,karl storbeck,haklar gonca,BEREKET ABDULLAH,GÜRAN TÜLAY, "17OH-Pregnenolone seems a major drive of androgen excess in patients with 11ß-hydroxylase deficiency", The 18th Adrenal cortex conference, 2018.
5. GÜRAN TÜLAY,KARA CENGİZ,yildiz melek,bitkin eda celebi,guven ayla,catli gonul,yesil gozde,haklar goncagul,onder sirikci,Lin JenChieh,Gilligan Lorna,Barnard Lisa,Storbeck Karl,Baris Tugba,Arlt Wiebke,BEREKET ABDULLAH, "Evaluation of molecular characteristics and steroid metabolomics in a large cohort of children with 3β-Hydroxysteroid Dehydrogenase 2 deficiency.", The 18th Adrenal cortex conference, 2018.
6. kashyap patel,colclough kevin,özbek mehmet nuri,yıldız melek,GÜRAN TÜLAY,koçyiğit cemil,ACAR SEZER,ŞIKLAR ZEYNEP,ATAR MÜGE,jonson matt,Flanagan Sarah E,Ellard Sian,ÇİZMECİOĞLU FİLİZ MİNE,BERBEROĞLU MERİH,DEMİR KORCAN,ÇATLI GÖNÜL,BAŞ SERPİL,akçay teoman,DEMİRBİLEK HÜSEYİN,weedon michael,Hattersley Andrew T, "Comprehensive Genetic Testing Shows One in FiveChildren with Diabetes and Non-Autoimmune Extra-Pancreatic Features Have Monogenic Aetiology.", 57th Annual Meeting of the ESPE, 2018.
7. ŞIKLAR ZEYNEP,DEMİRCİOĞLU SERAP,BEREKET ABDULLAH,ABACI AYHAN,BAŞ FİRDEVS,DEMİR KORCAN,GÜRAN TÜLAY,Akberzade Azad,BÖBER ECE,Özbek Mehmet Nuri,KARA CENGİZ,POYRAZOĞLU ŞÜKRAN,AYDIN HASAN MURAT,Kardelen Aslı,TARIM ÖMER FARUK,EREN ERDAL,HATİPOĞLU NİHAL,Büyükinan Muhammer,Akyürek Nesibe,ÇETİNKAYA SEMRA,Bayramoğlu Elvan,SELVER EKLİOĞLU BERAY,Uçaktürk Ahmet,ABALI SAYGIN,GÖKŞEN ŞİMŞEK RUHSAR DAMLA,Kor Yılmaz,Ünal Edip,ESEN İHSAN,YILDIRIM RUKEN,Akın Onur,Çay Atilla,DİLEK EMİNE,KİREL BİRGÜL,ANIK AHMET,ÇATLI GÖNÜL,BERBEROĞLU MERİH, "Nationwide Hypophosphatemic Rickets Study", 57th Annual Meeting of the ESPE, 2018. (Yayına Ulaşmak İçin Tıklayınız)
8. Kırkgöz Tarik,BAŞ SERPİL,YAVAŞ ABALI ZEHRA,DEMİRCİOĞLU SERAP,BEREKET ABDULLAH,GÜRAN TÜLAY, "Delayed Diagnosis of a Patient with Antley-Bixler Syndrome", HORMONE RESEARCH IN PAEDIATRICS, 2018.
9. KAYGUSUZ SARE BETÜL,ATAY ZEYNEP,KIRKGOZ TARIK,GÜRAN TÜLAY,BEREKET ABDULLAH,DEMİRCİOĞLU SERAP, "An Unusual Cause of Short Stature", HORMONE RESEARCH IN PAEDIATRICS 57th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 2018. (Yayına Ulaşmak İçin Tıklayınız)
10. YAVAŞ ABALI ZEHRA,YEŞİL GÖZDE,KIRKGOZ TARIK,KAYGUSUZ SARE BETÜL,DEMİRCİOĞLU SERAP,BEREKET ABDULLAH,GÜRAN TÜLAY, "Recurrent Hypoglycemia in a Preschooler Girl with Overgrowth: Isolated ACTH-Deficiency with a Novel TPIT Mutation", HORMONE RESEARCH IN PAEDIATRICS, 2018.
11. ozbek m nuri,doğan karaşin nezahat,DEMİRBİLEK HÜSEYİN,demiral meliha,BARAN RIZA TANER,GÜRAN TÜLAY, "Presenting Features, Clinical Characteristics andFollow Up of Familial Isolated GlucocorticoidDeficiency (FGD) Due to Mutations in MC2R andMRAP Genes", 57th Annual Meeting of ESPE (European Society for Pediatric Endocrinology, 2018.
12. GÜRAN TÜLAY,tezel başak,GÜRBÜZ FATİH,SELVER EKLİOĞLU BERAY,HATİPOĞLU NİHAL,KARA CENGİZ,şahin nuran,ŞİMŞEK ENVER,ÇİZMECİOĞLU FİLİZ MİNE,ÖZÖN ZEYNEP ALEV,BAŞ FİRDEVS,AYDIN HASAN MURAT,özdemir gülsüm,DARENDELİLER FATMA FEYZA, "Neonatal Screening for Congenital AdrenalHyperplasia in Turkey: A Pilot Study with 38,935Infants", 57th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), atina, 2018. (Yayına Ulaşmak İçin Tıklayınız)
13. GÜRAN TÜLAY,tezel başak,GÜRBÜZ FATİH,SELVER EKLİOĞLU BERAY,HATİPOĞLU NİHAL,KARA CENGİZ,şahin nuran,ŞİMŞEK ENVER,ÇİZMECİOĞLU FİLİZ MİNE,ÖZÖN ZEYNEP ALEV,BAŞ FİRDEVS,AYDIN HASAN MURAT,özdemir gülsüm,DARENDELİLER FATMA FEYZA, "Neonatal Screening for Congenital AdrenalHyperplasia in Turkey: A Pilot Study with 38,935Infants", 57th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), atina, 2018. (Yayına Ulaşmak İçin Tıklayınız)
14. GÜRAN TÜLAY,tezel başak,GÜRBÜZ FATİH,SELVER EKLİOĞLU BERAY,HATİPOĞLU NİHAL,KARA CENGİZ,şahin nuran,ŞİMŞEK ENVER,ÇİZMECİOĞLU FİLİZ MİNE,ÖZÖN ZEYNEP ALEV,BAŞ FİRDEVS,AYDIN HASAN MURAT,özdemir gülsüm,DARENDELİLER FATMA FEYZA, "Neonatal Screening for Congenital AdrenalHyperplasia in Turkey: A Pilot Study with 38,935Infants", 57th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 2018.
15. GÜRAN TÜLAY,Tezel Başak,GÜRBÜZ FATİH,SELVER EKLİOĞLU BERAY,HATİPOĞLU NİHAL,KARA CENGİZ,Sahin Nuran,ŞİMŞEK ENVER,ÇİZMECİOĞLU FİLİZ MİNE,Ozon Alev,BAŞ FİRDEVS,Aydın Murat,ÖZDEMİR İSMAİL,DARENDELİLER FATMA FEYZA, "Neonatal screening for congenital adrenal hyperplasia in Turkey: A pilot study with 38935 infants", 57th Annual Eurepean Society for Pediatric Endocrinology, Athens Greece, 2018.
16. ABACI AYHAN,ÇATLI GÖNÜL,kırbıyık özgür,şahin nursel,YAVAŞ ABALI ZEHRA,ünal edip,ŞIKLAR ZEYNEP,uçaktürk mengen eda,ÖZEN SAMİM,GÜRAN TÜLAY,KARA CENGİZ,yıldız melek,EREN ERDAL,nalbantoğlu özlem,GÜVEN AYLA,çayır atilla,DEMET AKBAŞ EMİNE,kor yılmaz,çürek yusuf,AYCAN ZEHRA,BAŞ FİRDEVS,DARCAN ŞÜKRAN,BERBEROĞLU MERİH, "PHENOTYPIC, HORMONAL AND MOLECULAR GENETIC CHARACTERISTICS OF 5-ALPHA REDUCTASE TYPE 2 DEFICIENCY PATIENTS: A MULTICENTER STUDY FROM TURKEY.", IMPE 2017, 2017.
17. Daniel E,Sandrk M,Blankenstein O,Neumann U,Grinten H,Linde A,DARENDELİLER FATMA FEYZA,POYRAZOĞLU ŞÜKRAN,Mendonca B,Bacheya T,Mirinde M,GÜRAN TÜLAY,Vieites A,Birkebaek N,Cools M,Milenkovic T,Bonfig W,Tomlinson J,Ahmed F,Elsedfy H,Balsamo A,Hannena S,Higham C,Atapatlo N,Lichiardopol C,Krone R,Mohnike K,Krone N, "Defining the dose, type and timing of glucocorticoid and mineralocorticoid replacement in 256 children and adults with CAH in the I-CAH registry", 10th International Meeting Of Pediatric Endocrinology, 2017.
18. GÜRAN TÜLAY,KARA CENGİZ,ATAY ZEYNEP,AKBARZADE AZAD,YILMAZ GÜLAY,ÇELEBİ BİTKİN EDA,AKÇAY TEOMAN,YILDIZ MELEK,GÜVEN AYLA,ÇATLI GÖNÜL,YEŞİL GÖZDE,BAS SERPİL,VATANSEVER PINAR,HAKLAR GONCAGÜL,ŞİRİKÇİ ÖNDER,TURAN SERAP,BEREKET ABDULLAH, "Evaluation of Clinical, Genetical, and Steroid Profile Features of Cases with 3Beta-Hydroxysteroid Dehydrogenase Type 2 Deficiency", American Association of Clinical Chemistry Congress, 2017.
19. KÜÇÜK NURAN,Abalı Saygın,CANPOLAT NUR,Akın Yasemin,Meriç İbrahim,Esmi Esma,Özçelik Gül,GÜRAN TÜLAY, "A RARE ENDOCRINE CAUSE OF HYPERTENSION: APPARENT MINERALOCORTICOID ACCESS SYNDROME", 50th Anniversary Meeting of the ESPN, 2017.
20. GÜVEN AYLA,GÜRAN TÜLAY,KRONE N, "17-Hydroxlase deficiency: Rare Cause of Delayed Puberty", 10th International Meeting of Pediatric Endocrinology, 2017.
21. GÜVEN AYLA,BUONOCORE F,ACHERMANN J,GÜRAN TÜLAY, "CYP11A1 mutations Results Various Clinical Phenotypes.", 10th International Meeting of Pediatric Endocrinology, 2017.
22. EREN ERDAL,ERGÜR AYÇA,İŞGÜVEN ŞÜKRİYE PINAR,ÇELEBİ BİTKİN EDA,BERBEROĞLU MERİH,ŞIKLAR ZEYNEP,genens MİKAYİR,DOĞAN MURAT,YEL SERVET,BAŞ SERPİL,SOBU ELİF,BEREKET ABDULLAH,TURAN SERAP,SAĞLAM HALİL,ATAY ZEYNEP,ERCAN OYA,GÜRAN TÜLAY,ATABEK MEHMET EMRE,korkmaz hüseyin anıl,KILINÇ UĞURLU AYLİN,AKINCI AYŞEHAN,DÖĞER ESRA,ŞİMŞEK ENVER,DEMET AKBAŞ EMİNE,YEŞİLKAYA EDİZ,ABACI AYHAN,GÜL ÜLKÜ,ACAR SEZER,uçaktürk mengen eda,yıldız melek,ünal edip,TARIM ÖMER FARUK, "CLINICAL AND LABORATORY CHARACTERISTICS OF HYPERPROLACTINEMIC CHILDREN AND ADOLESCENTS: NATIONAL SURVEY.", IMPE 2017, 2017.
23. BAS SERPIL,GÜRAN TÜLAY,ATAY ZEYNEP,HALILOGLU BELMA,ABALI SAYGIN,TURAN SERAP,BEREKET ABDULLAH, "Premature Pubarche Hyperinsulinemia Hypothyroxinemia and Hyperintensities in Basal Ganglia All Caused by a Single Congenital Defect", Current Trends in Pediatric Endocrinology- A PES perspective, 2016. (Yayına Ulaşmak İçin Tıklayınız)
24. Prasad RR,Hadjidemetriou II,Avinaash Maharaj A,Meimaridou EE,Van Veldhoven PP,Buonocore FF,Moin Saleem MM,Hurcombe JJ,Bierzynska AA,Barbagelata EE,Bergada II,Cassinelli HH,Das UU,GOSgene GOSgene,Ruth Krone,Hacihamdioglu BB,Sari EE,Yesilkaya EE,Storr HL,Clemente MM,FernandezCancio MM,Camats NN,Ram NN,Achermann JC,Guasti LL,Braslavsky DD,GÜRAN TÜLAY,Metherell LA, "Mutations in SGPL1 cause a novel form of primary adrenal insufficiency with steroid resistant nephrotic syndrome", 55.TH ESPE-Paris-France, 10-12 September, 2016. (Yayına Ulaşmak İçin Tıklayınız)
25. Ozcan Sibel,ABALI SAYGIN,ATAY ZEYNEP,HALILOGLU BELMA,Bas Serpil,Ozturk Gamze,Cam Sevda,Akcay Teoman,GÜRAN TÜLAY,BEREKET ABDULLAH,TURAN SERAP, "Etiologic Distribution and Characteristics of Patients with Short Stature in a Pediatric Endocrinology Clinic", 55.TH ESPE-Paris-France, 10-12 September, 2016. (Yayına Ulaşmak İçin Tıklayınız)
26. BEREKET ABDULLAH,Bugur Ibrahim Sinan,GÜRAN TÜLAY,Atay Zeynep,Ekberzade Azad,Gurbanov Ziya,Oge Ece,Tas Cektar Seyid Riza,TURAN SERAP,FURMAN ANDRZEJ, "Reconsideration of Mid Parental Height Calculation", 55.TH ESPE-Paris-France, 10-12 September, 2016.
27. Ekberzade Azad,ABALI SAYGIN,Atay Zeynep,Bas Serpil,Gurbanov Ziya,TURAN SERAP,GÜRAN TÜLAY,BEREKET ABDULLAH, "b hCG from an Occult Source Causing Peripheral Precocious Puberty Identification of the Tumour 6 Years After Presentation", 55.TH ESPE-Paris-France, 10-12 September, 2016. (Yayına Ulaşmak İçin Tıklayınız)
28. Bas Firdevs,Abali Zehra Yavas,GÜRAN TÜLAY,Genens Mikayir,Poyrazoglu Sukran,bundak ruveyde,DARENDELİLER FATMA FEYZA, "Precocious Puberty in Patients with Primary Adrenal Insufficiency due to Melanocortın Receptor 2 Mutation", 55.TH ESPE-Paris-France, 10-12 September, 2016. (Yayına Ulaşmak İçin Tıklayınız)
29. Kourime Mariam,Bryce Jillian,Jiang Jipu,Karunasena Nayananjani,GÜRAN TÜLAY,Hannema Sabine Elisabeth,Cool Martine,Hedi L Claahsen Van Der Grinten,Krone Nils,DARENDELİLER FATMA FEYZA,Balsamo Antonio,Bonfig Walter,Nordenstrom Anna,Hiort Olaf,Dagmar Lallemand,Ross Richard,Syed Faisal Ahmed,Koehler Birgit,Acerini Carlo,Mendonca Berenice B,Bertelloni Silvano,Lisa Lidka,Elsedfy Heba,Marginean Otilia, "A New International Registry Highlights the Differences in Practice for Reaching a Diagnosis of CAH On Behalf of the I CAH I DSD Registry User Group", 55.TH ESPE-Paris-France, 10-12 September, 2016. (Yayına Ulaşmak İçin Tıklayınız)
30. Lindhardt Johansen Marie,Acerini Carlo,Andrade Juliana,Balsamo Antonio,Cools Martine,Cools Martine,Cuccaro Rieko Tadokoro,DARENDELİLER FATMA FEYZA,Fluck Christa E,Grinspon Romina,GÜRAN TÜLAY,Hannema Sabine,LucasHerald Angela K,Hiort Olaf,Lichiardopol Corina,Ortolano Rita,Riedl Stefan,Ahmed S Faisal,Juul Anders, "A Multicenter Study on Long Term Outcomes in 56 Males with 45 X 46 XY Mosaicism", 55.TH ESPE-Paris-France, 10-12 September, 2016. (Yayına Ulaşmak İçin Tıklayınız)
31. Bas Serpil,Akbarzade Azad,Atay Zeynep,Gurbanov Ziya,GÜRAN TÜLAY,TURAN SERAP,De Franco Elisa,Ellard Sian,BEREKET ABDULLAH, "Thiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine", 55.TH ESPE-Paris-France, 10-12 September, 2016. (Yayına Ulaşmak İçin Tıklayınız)
32. ABALI SAYGIN,ARMAN AHMET,ATAY ZEYNEP,BEREKET ABDULLAH,BAS SERPIL,HALILOGLU BELMA,GÜRAN TÜLAY,Gormez Zeliha,Demirci Huseyin,AKARSU AYŞE NURTEN,TURAN SERAP, "Frequency of Recessive Osteogenesis Imperfecta in a Turkish Cohort and Genetic Causes", 55.TH ESPE-Paris-France, 10-12 September, 2016. (Yayına Ulaşmak İçin Tıklayınız)
33. Karunasena Nayananjani,Daniel Eleni,Bryce Jillian,Jiang Jipu,S Faisal Ahmed,GÜRAN TÜLAY,ET AL,Klaus Mohnike,Heba Elsedfy,Ross Richard, "Adrenal crisis and sick day episodes among CAH patients preliminary report based on International CAH I CAH registry", 18th European Congress of Endocrinology meeting, Munich, 28-31 May 2016, 2016. (Yayına Ulaşmak İçin Tıklayınız)
34. Prasad RR,Hadjidemetriou II,Avinaash Maharaj A,Meimaridou EE,Van Veldhoven PP,Buonocore FF,Moin Saleem MM,Hurcombe JJ,Bierzynska AA,Barbagelata EE,Bergada II,Cassinelli HH,ET AL,Braslavsky DD,GÜRAN TÜLAY,METHERELL LA, "Mutations in SGPL1 causing sphingosine 1 phosphate lyase deficiency cause a novel form of primary adrenal insufficiency with steroid resistant nephrotic syndrome", SfE British Endocrine Society, 2016, 7-9 November, Brighton, United Kingdom, 2016. (Yayına Ulaşmak İçin Tıklayınız)
35. Baranowski Elizabeth S,Bunte Kerstin,Shackleton Cedric HL,Taylor Angela E,Hughes Beverly A,Biehl Michael,Tino Peter,GÜRAN TÜLAY,Wiebke Arlt, "Steroid metabolomics for diagnosis of inborn steroidogenic disorders bridging the gap between biochemist and clinician through computational approaches", SfE British Endocrine Society, 2016. (Yayına Ulaşmak İçin Tıklayınız)
36. Zaucker AA,Griffin AA,Storbeck KarlHeinz,GÜRAN TÜLAY, "A Novel Animal Model to Study 21 Hydroxylase Deficiency in vivo", HORMONE RESEARCH IN PAEDIATRICS, 55.TH ESPE-Paris-France, 10-12 September, 2016.
37. Prasad RR,Hadjidemetriou II,Avinaash Maharaj A,et al,Braslavsky DD,GÜRAN TÜLAY,Metherell LA, "Mutations in SGPL1 the Gene Encoding Sphingosine 1 Phosphate Lyase Cause a Novel Form of Primary Adrenal Insufficiency with Steroid Resistant Nephrotic Syndrome", HORMONE RESEARCH IN PAEDIATRICS, 55.TH ESPE-Paris-France, 10-12 September, 2016. (Yayına Ulaşmak İçin Tıklayınız)
38. GÜRAN TÜLAY, "Urinary steroid Profiling", Disorders of Sex Development (DSD)- the roles of genes and the environment’PhD course, Copenhagen, 2015. (Yayına Ulaşmak İçin Tıklayınız)
39. ABACI AYHAN,ÇATLI GÖNÜL,Kırbıyık Özgür,ŞAHİN NURSEL MURATOĞLU,ABALI ZEHRA YAVAŞ,ÜNAL EDİP,ŞIKLAR ZEYNEP,MENGEN EDA,ÖZEN SAMİM,GÜRAN TÜLAY,KARA CENGİZ,YILDIZ MELEK,EREN ERDAL,NALBANTOPĞLU ÖZLEM,GÜVEN AYLA,ÇAYIR ATİLLA,AKBAŞ EMİNE DEMET,KOR YILMAZ,ÇÜREK YUSUF,AYCAN ZEHRA,BAŞ FİRDEVS,DARCAN ŞÜKRAN,BERBEROĞLU MERİH, "Characteristics in 5-Alpha Reductase Type 2 Deficiency: A Multicenter Study from Turkey.", 10th International Meeting of Pediatric Endocrinology, 2017. (Yayına Ulaşmak İçin Tıklayınız)
40. DÖĞER ESRA,KILINÇ UĞURLU AYLİN,KAZANCIOĞLU ALP,DEMET AKBAŞ EMİNE,GÜRAN TÜLAY,BİDECİ AYSUN,ÇAMURDAN MAHMUT ORHUN,CİNAZ PEYAMİ, "aldosterone synthase deficiency: a new mutation", 10. İnternational meeting of pediatric endocrinology, washington, 2017.
41. BİDECİ AYSUN,DÖĞER ESRA,DEMET AKBAŞ EMİNE,KILINÇ UĞURLU AYLİN,GÜRAN TÜLAY,ÇAMURDAN MAHMUT ORHUN,CİNAZ PEYAMİ, "familial glucocortıcoid deficiency type 2: a new mutation in the mrap gene p. k30del", 10. international meeting of pediatric endocrinology, washington, 2017.
42. Baranowski Elizabeth S,Kerstin Bunte,Shackleton Cedric HL,Taylor Angela E,Hughes Beverley A,Biehl Michael,Tino Peter,GÜRAN TÜLAY,arlt wiebke, "MAPPING THE STEROID METABOLOME IN INBORN STEROIDOGENIC DISORDERS: PERFORMANCE OF A NOVEL COMPUTATIONAL APPROACH IN COMPARISON TO CONVENTIONAL GC-MS ANALYSIS.", 10th Individual Abstracts for International Meeting of Pediatric Endocrinology, 2017.
43. Yildiz Melek,TURAN SERAP,akcay teoman,atay zeynep,onal hasan,baris tugba,haklar goncagul,BEREKET ABDULLAH,GÜRAN TÜLAY, "17OH-PREGNENOLONE SEEMS A MAJOR DRIVE OF ANDROGEN EXCESS IN PATIENTS WITH 11ß-HYDROXYLASE DEFICIENCY", . 10th Individual Abstracts for International Meeting of Pediatric Endocrinology, 2017.
44. Enver Ece Öge,Vatansever Pinar,Guran Omer,BORAN PERRAN,TURAN SERAP,Haklar Goncagul,BEREKET ABDULLAH,GÜRAN TÜLAY, "SIMULTANEOUS PROFILING OF 17 STEROID HORMONES USING LIQUID CHROMATOGRAPHY TANDEM MASS SPECTROMETRY IN NEWBORN AND EARLY INFANCY.", 10th Individual Abstracts for International Meeting of Pediatric Endocrinology, 2017.
45. Prasad R,Hadjidemetriou I,Avinaash Maharaj A,Meimaridou E,Van Veldhoven PP,Buonocore F,Moin Saleem M,Hurcombe J,Bierzynska A,Barbagelata E,Bergada I,Cassinelli H,Das U,GOS gene,Krone R Ruth,Hacihamdioglu B,Sari E,Yesilkaya E,Storr HL,Clemente M,Fernandez Cancio M,Camats N,Ram N,Achermann JC,Guasti L,Braslavsky D,GÜRAN TÜLAY,Metherell LA, "Mutations in SGPL1, causing sphingosine-1-phosphate lyase deficiency, cause a novel form of primary adrenal insufficiency with steroid resistant nephrotic syndrome.", ENDO 2017, 2017.
46. Baranowski Elizabeth,Bunte Kerstin,Shackleton Cedric H L,Taylor Angela E,Hughes Beverley A,Biehl Michael,Tino Peter,GÜRAN TÜLAY,Arlt Wiebke, "Steroid metabolomics for accurate and rapid diagnosis of inborn steroidogenic disorders", 19th European Congress of Endocrinology., 2017.
47. LucasHerald A,Kyriakou A,Bryce J,Rodie M,C Acerini,Arlt W,Audi L,Balsamo A,Bertelloni S,Brooke A B,Chatelain P,Cools M,Lichiardopol C,DARENDELİLER FATMA FEYZA,Li D,Elliathi M,Fica S,Gawlik A,Claahsen HA,GÜRAN TÜLAY,Hannema S,Hewitt J,Hiort O,Holterhus PM,Iotova V,Jennane F,Johnston C,Krone R,Lachlan K,Lisa L,Mazen I,Mohnike K,Niedziela M,Nordenstrom A,Rey R,Vries L De,Weintrob N,SF Ahmed, "Characterisation of adults at risk of long-term, early onset hypogonadism In the International Disorders of Sex Development Registry", 6th International Symposium Disorders of Sex Development., 2017.
48. ABACI AYHAN,ÇATLI GÖNÜL,KIRBIYIK ÖZGÜR,ŞAHİN NURSEL M,Y ABALI ZEHRA,ÜNAL EDİP,ŞIKLAR ZEYNEP,MENGEN EDA,ÖZEN SAMİM,GÜRAN TÜLAY,KARA CENGİZ,YILDIZ METİN,EREN ERDAL,NALBANTOĞLU ÖZLEM,GÜVEN AYLA,ÇAYIR ATİLLA,AKBAŞ EMİNE DEMET,KÖR YILMAZ,ÇÜREK YUSUF,AYCAN ZEHRA,BAŞ FİRDEVS,DARCAN ŞÜKRAN,BERBEROĞLU MERİH, "PHENOTYPIC, HORMONAL AND MOLECULAR GENETIC CHARACTERISTICS OF 5-ALPHA REDUCTASE TYPE 2 DEFICIENCY PATIENTS: AMULTICENTER STUDY FROM TURKEY", 10.th International Meeting of Pediatric Endocrinology, WASHINGTON, 2018.
49. Lucas Herald Angela K,Kyriakou Andreas,Bryce Jillian,Martina Rodie,Carlo Acerini,Arlt Wiebke,Audi Laura,Balsamo Antonio,Bertelloni Silvano,Brooke Antonia,Chatelain Pierre,Van Der Grinten Hedi Claahsen,Cools Martine,DARENDELİLER FATMA FEYZA,Davies Justin H,Ellaithi Mona,Fica Simona,Gawlik Aneta M,GÜRAN TÜLAY,Hannema Sabine E,Jacqueline Hewitt,Hiort Olaf,Holterhus Paul Martin,Lotova Violeta,Jennane Farida,Johnston Colin,Krone E Ruth,Lachlan Katherine,Dejun Li,Lichiardopol Corina,Lidka Lisa,Mazen Inas,Mohnike Klaus,Niedziela Marek,Nordenstrom Anna,Rodolfo A Rey,De Vries Liat,Weintrob Naomi,Ahmed Faisal S, "The prevalence of adults with SDS conditions at risk of hypogonadism in the international disorders of sex development registry", 10 th International Meeting of Pediatric Endocrinology, 2017.
50. GuaragnaFilho G,Junior G Guerra,Darendeliler F,Balsamo A,Holterhus PM,GÜRAN TÜLAY,AHMED SF,Quigley CA, "Pubertal Development in Individuals with Partial Androgen Insensitivity Syndrome PAIS Assigned Female Sex of Rearing", 5th I-DSD Symposium, Ghent, 2015.
51. Baetens Dorien,GÜRAN TÜLAY,De Cauwer Lode,Looijenga Leendert,De Bosscher Karolien,Cools Martine,De Baere Elfride, "Identification and functional characterization of ESR2 a new disease gene for 46 XY disorders of sex development DSD", 5th I-DSD Symposium, Ghent, 2015. (Yayına Ulaşmak İçin Tıklayınız)
52. BAS SERPIL,ABALI SAYGIN,ATAY ZEYNEP,HALILOGLU BELMA,GURBANOV ZIYA,GÜRAN TÜLAY,BEREKET ABDULLAH,TURAN SERAP, "Factors Effecting Response to Growth Hormone Treatment in Children with Turner Syndrome", 54th ESPE (European Society of Pediatric Endocrinology) meeting, Barselona, 2015. (Yayına Ulaşmak İçin Tıklayınız)
53. ABALI SAYGIN,BAS SERPIL,AKBARZADE AZAD,ATAY ZEYNEP,HALILOGLU BELMA,GÜRAN TÜLAY,TURAN SERAP,BEREKET ABDULLAH, "Evaluating First Year Response and Final Height to Growth Hormone Treatment in Growth Hormone Deficiency Based on Peak GH Levels on Testing", 54th ESPE (European Society of Pediatric Endocrinology), Barselona, 2015. (Yayına Ulaşmak İçin Tıklayınız)
54. CETINKAYA SEMRA,GÜRAN TÜLAY,ERDAL KURNAZ,Keskin Meliksah,Sagsak Elif,Savas Erdeve Senay,Buonocore Federica,AYCAN ZEHRA, "A novel mutation cdel209 in the proopiomelanocortin gene in a child with early onset obesity", 54th ESPE (European Society of Pediatric Endocrinology) meeting, Barselona, 2015. (Yayına Ulaşmak İçin Tıklayınız)
55. Poyrazoglu Sukran,Darendeliler Feyza,Ahmed Syed Faisal,Bryce Jillian,Rodie Martina,Jiang Jipu,Hiort Olaf,E Hannemad Sabine,Bertellonie Silvano,Lisa Lidka,GÜRAN TÜLAY,Hughes Ieuan,Cools Martine,Chatelain Pierre,van der Grinten Hedi L Claahsen,Nordenstrom Anna,Holterhus Paul Martin,Köhler Birgit,Niedziela Marek,Krone Nils, "Birthweight in different etiologies of disorder of sex development", 54th ESPE (European Society of Pediatric Endocrinology) meeting, Barselona, 2015. (Yayına Ulaşmak İçin Tıklayınız)
56. Abali Saygin,TAMURA S,ATAY ZEYNEP,GURAN TULAY,ISGUVEN PINAR,HALILOGLU BELMA,BAS SERPIL,GÜRAN TÜLAY,Isojima T,TURAN SERAP,Kitanaka S,BEREKET ABDULLAH, "Hereditary Vitamin D resistant Rickets Report of Four Cases with Successful use of intermittant intravenous calcium via peripheral route", 54th ESPE (European Society of Pediatric Endocrinology) meeting, Barselona, 2015. (Yayına Ulaşmak İçin Tıklayınız)
57. ATAY ZEYNEP,YESILKAYA EDIZ,SAVAS ERDEVE SENAY,AKIN LEYLA,EREN ERDAL,DOGER ESRA,AYCAN ZEHRA,YAVAS ABALI ZEHRA,AKINCI AYSEHAN,SIKLAR ZEYNEP,OZEN SAMIM,KARA CENGIZ,TAYFUN MELTEM,TUTUNCULER FILIZ,SEYMEN KARABULUT GULCAN,KARAGUZEL GULAY,SAGLAM HALIL,BIDECI AYSUN,KURTOGLU SELIM,BEREKET ABDULLAH,TURAN SERAP,SARI ERKAN,CETINKAYA SEMRA,GÜRAN TÜLAY, "Aetiological spectrum and clinical characteristics of 129 children with gonadotropin independent precocious puberty A nationwide cohort study", 54th ESPE (European Society of Pediatric Endocrinology) meeting, Barselona, 2015. (Yayına Ulaşmak İçin Tıklayınız)
58. GÜRAN TÜLAY,Buonocore F,SAKA N,Ozbek MN,Aycan Z,BEREKET ABDULLAH,BAS F,Darcan S,BİDECİ AYSUN,GUVEN A,DEMİR KORCAN,AKINCI A,Buyukinan M,Kucukemre Aydin B,TURAN SERAP,Yilmaz Agladioglu S,ATAY Z,Yavas Abali Z,TARIM O,Catli G,YUKSEL B,AKCAY T,YILDIZ M,OZEN S,DOGER E,DEMİRBİLEK HÜSEYİN,UCAR A,ISIK E,OZHAN B,BOLU SEMİH,OZGEN T,Suntharalingham J,ACHERMANN JC, "Rare causes of primary adrenal insufficiency Genetic and clinical characterization of a large nationwide cohort", 54th ESPE (European Society of Pediatric Endocrinology) meeting, Barcelona, 2015. (Yayına Ulaşmak İçin Tıklayınız)
59. LucasHerald A,AHMED SF,Bertelloni S,JUUL A,BRYCE J,Jiang J,RODIE M,Johansen ML,Hiort O,Holterhus PM,COOLS M,Desloovere A,Weintrob N,Hannema S,DROP SL,GÜRAN TÜLAY,Poyrazoglu S,Darendeliler F,Nordenstrom A,TadokoroCuccaro R,Hughes I,Acerini CL, "Long Term Endocrine Outcome In Men With Partial Androgen Insensitivity Syndrome", 54.th ESPE (European Society of Pediatric Endocrinology) meeting-BARCELONA-SPAIN, Barcelona, 2015. (Yayına Ulaşmak İçin Tıklayınız)
ULUSAL
60. GÜRAN TÜLAY,BAS FIRDEVS,GOKCAY GULDEN,Hughes Beverly A,KAYSERİLİ KARABEY HÜLYA,Shackleton Cedric H,Arlt Wiebke, "5 Reduktaz tip 3 eksikliginin insan steroid metabolizmasina etkisi", XIX. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Istanbul, 2015. (Yayına Ulaşmak İçin Tıklayınız)
61. CETINKAYA SEMRA,AYCAN ZEHRA,GÜRAN TÜLAY,KURNAZ ERDAL,Keskin Melikşah,Sağsak Elif,Savaş Erdeve Şenay,ACHERMANN JOHN, "PROOPİOMELANOKORTİN POMC GENİNDE YENİ MUTASYONLU ERKEN BAŞLANGIÇLI BİR OBEZİTE OLGUSU", Ulusal Cocuk Endokrinoloji Dernegi 7. Olgu sunumlari toplantisi, Izmir, 2015.
62. TURAN SERAP,BAS SERPIL,Akay Tayfun GULSEN,ABALI SAYGIN,ATAY ZEYNEP,Qurbanov ZIYA,CAM SEVDA,HURIYE NURSEL ELCIOGLU,GÜRAN TÜLAY,BEREKET ABDULLAH, "ANTLEY BİXLER SENDROMLU BİR OLGUMUZ", Cocuk Endokrinoloji Dernegi 7.Olgu Sunumlari Toplantisi, Izmir, 2015.
63. KILINÇ UĞURLU AYLİN,DÖĞER ESRA,KAZANCIOĞLU ALP,DEMET AKBAŞ EMİNE,GÜRAN TÜLAY,BİDECİ AYSUN,ÇAMURDAN MAHMUT ORHUN,CİNAZ PEYAMİ, "Aldosteron sentaz eksikliği: yeni bir mutasyon", 21. ulusal pediatrik endokrinoloji ve diyabet kongresi, Antalya, 2017.
64. GÜRAN TÜLAY,tezel başak,GÜRBÜZ FATİH,SELVER EKLİOĞLU BERAY,HATİPOĞLU NİHAL,KARA CENGİZ,ŞİMŞEK ENVER,şahin nuran,ÇİZMECİOĞLU FİLİZ MİNE,ALKAN AFRA,özon alev,BAŞ FİRDEVS,özdemir gülsüm,AYDIN HASAN MURAT,DARENDELİLER FATMA FEYZA, "Türkiye`de Konjenital Adrenal Hiperplazi Yenidoğan Taraması: 38.936 Bebeği Kapsayan Pilot Çalışma Verilerinin Değerlendirilmesi", XXII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, 2018. (Yayına Ulaşmak İçin Tıklayınız)
65. ABACI AYHAN,ÇATLI GÖNÜL,KIRBIYIK Ö,MURATOĞLU ŞAHİN N,YAVAŞ ABALI ZEHRA,ÜNAL E,ŞIKLAR ZEYNEP,UÇAKTÜRK MENGEN E,ÖZEN SAMİM,GÜRAN TÜLAY,KARA CENGİZ,YILDIZ M,EREN ERDAL,NALBANTOĞLU Ö,GÜVEN AYLA,ÇAYIR ATİLLA,AKBAŞ ED,KOR Y,CÜREK Y,AYCAN ZEHRA,BAŞ FİRDEVS,DARCAN ŞÜKRAN,BERBEROĞLU MERİH, "5-alfa redüktaz tip 2 eksikliği tanılı olguların fenotipik, hormonal ve moleküler genetik özellikleri: Çok merkezli ulusal veriler", XXI. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, ANTALYA, 2017.
66. DÖĞER ESRA,DEMET AKBAŞ EMİNE,KILINÇ UĞURLU AYLİN,GÜRAN TÜLAY,BİDECİ AYSUN,ÇAMURDAN MAHMUT ORHUN,CİNAZ PEYAMİ, "Ailevi glukokortikoid eksikliği tip 2: MRAp geninde yeni mutasyon p.K30del", 21. ulusal pediatrik endokrinoloji ve diyabet kongresi, Antalya, 2017.
67. GÜRAN TÜLAY, "Idrar steroid profili", XIX. ULUSAL PEDIATRIK ENDOKRINOLOJI KONGRESI, Istanbul, 2015. (Yayına Ulaşmak İçin Tıklayınız)
68. OZCAN SIBEL,ABALI SAYGIN,ATAY ZEYNEP,BELMA HALILOGLU,BAS SERPIL,Öztürk Gamze,SEVDA CAM,AKCAY TEOMAN,GÜRAN TÜLAY,TURAN SERAP,BEREKET ABDULLAH, "Boy Kısalığı Olan Hastalarda Özellikler ve Etiyolojik Dağılım Bir Çocuk Endokrinoloji Kliniği Verileri", XIX.Ulusal Pediatrik Endokrinoloji Kongresi, Istanbul, 2015. (Yayına Ulaşmak İçin Tıklayınız)
69. ABALI SAYGIN,AKCAN NESE,Toksoy Güven,ATAY ZEYNEP,UYGUNER ZEHRA OYA,BAS FIRDEVS,GÜRAN TÜLAY,BAS SERPIL,Kırmızıbekmez Heves,POYRAZOĞLU ŞÜKRAN,KAYSERİLİ KARABEY HÜLYA,TURAN SERAP,DARENDELİLER FATMA FEYZA, "Nonklasik Konjenital Adrenal Hiperplazi Hastalarının Genotip Ve Fenotip Özellikleri", XIX. Ulusal Pediatrik Endokrinoloji Kongresi, Istanbul, 2015. (Yayına Ulaşmak İçin Tıklayınız)
70. ABALI SAYGIN,ARMAN AHMET,ATAY ZEYNEP,BAS SERPIL,GÜRAN TÜLAY,GORMEZ ZELIHA,DEMIRCI HUSEYIN,AKARSU AYŞE NURTEN,BEREKET ABDULLAH,TURAN SERAP, "Otozomal Resesif Osteogenezis İmperfekta Populasyonumuzdaki Sıklığı Ve Genetik Nedenleri", XIX. Ulusal Pediatrik Endokrinoloji Kongresi, Istanbul, 2015. (Yayına Ulaşmak İçin Tıklayınız)
71. ATAY ZEYNEP,YESILKAYA EDIZ,Savas Erdeve Senay,Akin Leyla,EREN ERDAL,ESRA DOGER,DOGER ESRA,AYCAN ZEHRA,YAVAS ABALI ZEHRA,AYSEHAN AKINCI,SIKLAR ZEYNEP,OZEN SAMIM,KARA CENGIZ,TAYFUN MELTEM,Tutunculer Filiz,SEYMEN KARABULUT GÜLCAN,KARAGÜZEL GÜLAY,SAĞLAM HALİL,BIDECI AYSUN,KURTOGLU SELIM,BEREKET ABDULLAH,TURAN SERAP,SARI ERKAN,Cetinkaya Semra,GÜRAN TÜLAY, "Periferal Puberte Prekokslu 129 Çocukta Etiyolojik Dağılım ve Klinik Özellikler", XIX. Ulusal Pediatrik Endokrinoloji Kongresi, Istanbul, 2015. (Yayına Ulaşmak İçin Tıklayınız)
72. GÜRAN TÜLAY,Taylor Angela,Hughes Beverly A,ONeill Donna,Cedric Shackleton,Arlt Wiebke, "5 Reduktaz tip 2 eksikligi tanisinda GC MS ile steroid olcumlerinde diagnostik oranlarin normatif datasinin olusturulmasi", XIX. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Istanbul, 2015. (Yayına Ulaşmak İçin Tıklayınız)
73. GÜRAN TÜLAY,Shafqat Naeem,Taylor Angela,Bujalska Iwona,Ivison Hannah,Wiebke Arlt, "5 Reduktaz tip 2 eksikligine yol acan yeni mutasyonlarin molekuler karakterizasyonu", XIX. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Istanbul, 2015. (Yayına Ulaşmak İçin Tıklayınız)
74. GÜRAN TÜLAY,ZAUCKER ANDREAS,TAYLOR ANGELA,Doultsinos Dimitrios,Griffin Aliesha,Mueller Ferenc,Krone Nils, "Zebra baliginda zCyp21a2 geninin karakterizasyonu", XIX. Ulusal Pediatrik Endokrinoloji, Istanbul, 2015. (Yayına Ulaşmak İçin Tıklayınız)
75. ABACI AYHAN,ÇATLI GÖNÜL,KIRBIYIK ÖZGÜR,MURATOĞLU ŞAHİN NURSEL,YAVAŞ ABALI ZEHRA,ÜNAL EDİP,ŞIKLAR ZEYNEP,MENGEN UÇAKTÜRK EDA,ÖZEN SAMİM,GÜRAN TÜLAY,KARA CENGİZ,YILDIZ MELEK,EREN ERDAL,NALBANTOĞLU ÖZLEM,GÜVEN AYLA,ÇAYIR ATİLLA,AKBAŞ EMİNE DEMET,KÖR YILMAZ,CÜREK YUSUF,AYCAN ZEHRA,BAŞ FİRDEVS,DARCAN ŞÜKRAN,BERBEROĞLU MERİH, "5-Alfa Redüktaz Tip 2 Eksikliği Tanılı Olguların Fenotipik, Hormonal veMoleküler Genetik Özellikleri: Çok Merkezli Ulusal Veriler", XX1.ULUSAL PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, 2018.
YAYINLANMAMIŞ BİLDİRİLER
ULUSLARARASI
1. ŞIKLAR ZEYNEP,TURAN SERAP,BEREKET ABDULLAH,ABACI AYHAN,BAŞ FİRDEVS,DEMİR KORCAN,GÜRAN TÜLAY,AKBERZADE AZAD,BÖBER ECE,ÖZBEK MEHMET N,KARA CENGİZ,POYRAZOĞLU ŞÜKRAN,AYDIN HASAN MURAT,KARDELEN ASLI,TARIM ÖMER FARUK,EREN ERDAL,HATİPOĞLU NİHAL,BÜYÜKİNAN MUAMMER,AKYÜREK NESİBE,ÇETİNKAYA SEMRA,BAYRAMOĞLU ELVAN,EKLİOĞLU BERAY SELVER,UCAKTÜRK AHMET,ABALI SAYGIN,GÖKŞEN ŞİMŞEK RUHSAR DAMLA,KÖR YILMAZ,ÜNAL EDİP,ESEN İHSAN,YILDIRIM RUKEN,AKIN ONUR,CAYIR ATİLLA,DİLEK EMİNE,KİREL BİRGÜL,ANIK AHMET,ÇATLI GÖNÜL,BERBEROĞLU MERİH, "Nationwide Hypophosphatemic Rickets Study", 57.th Annual Meeting of the European Society for Paediatric Endocrinology(ESPE), ATİNA
ULUSAL
2. SAVAŞ ERDEVE ŞENAY,ÇETİNKAYA SEMRA,YAVAŞ ABALI ZEHRA,POYRAZOĞLU ŞÜKRAN,BAŞ FİRDEVS,BERBEROĞLU MERİH,ŞIKLAR ZEYNEP,KORKMAZ ÖZLEM,BULUŞ DERYA,DEMET AKBAŞ EMİNE,GÜRAN TÜLAY,BÖBER ECE,AKIN ONUR,CAN YILMAZ GÜLAY,AYCAN ZEHRA, "21 HİDROKSİLAZ EKSİKLİĞİNE BAĞLI KLASİK OLMAYAN KONJENİTAL ADRENAL HİPERPLAZİDE KLİNİK, LABORATUVAR, GENETİK ÖZELLİKLER, TEDAVİYE ALINAN YANITLAR VE ULAŞILAN FİNAL BOY VERİLERİ", 22. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET DERNEĞİ, ANTALYA
3. ŞIKLAR ZEYNEP,TURAN SERAP,BEREKET ABDULLAH,ABACI AYHAN,GÜRAN TÜLAY,DEMİR KORCAN,AKBERZADE AZAD,BAŞ FİRDEVS,BÖBER ECE,ÖZBEK MEHMET NURİ,KARA CENGİZ,POYRAZOĞLU ŞÜKRAN,AYDIN MURAT,KARDELEN ASLI,TARIM ÖMER FARUK,EREN ERDAL,HATİPOĞLU NİHAL,BÜYÜKİNAN MUAMMER,AKYÜREK NESİBE,ÇETİNKAYA SEMRA,BAYRAMOĞLU ELVAN,SELVER EKLİOĞLU BERAY,UÇAKTÜRK AHMET,ABALI SAYGIN,KOR YILMAZ,ÜNAL EDİP,ESEN İHSAN,YILDIRIM RUKEN,AKIN ONUR,ÇAY ATİLLA,DİLEK EMİNE,KIRAL BİRGÜL,ANIK AHMET,BERBEROĞLU MERİH, "Çok Merkezli Olarak Hipofosfatemik Riketsli Olguların Değerlendirilmesi", 22. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, ANTALYA
4. ŞIKLAR ZEYNEP,TURAN SERAP,BEREKET ABDULLAH,ABACI AYHAN,GÜRAN TÜLAY,DEMİR KORCAN,AKBARZADE AZAD,BAŞ FİRDEVS,BÖBER ECE,ÖZBEK MEHMET NURİ,KARA CENGİZ,POYRAZOĞLU ŞÜKRAN,AYDIN HASAN MURAT,KARDELEN ASLI,TARIM ÖMER FARUK,EREN ERDAL,HATİPOĞLU NİHAL,BÜYÜKİNAN MUAMMER,AKYÜREK NESİBE,ÇETİNKAYA SEMRA,BAYRAMOĞLU ELVAN,EKLİOĞLU BERAY SELVER,UÇAKTÜRK AHMET,ABALI SAYGIN,GÖKŞEN ŞİMŞEK RUHSAR DAMLA,KÖR YILMAZ,ÜNAL EDİP,ESEN İHSAN,YILDIRIM RUKEN,AKIN ONUR,ÇAYIR ATİLLA,DİLEK EMİNE,KİREL BİRGÜL,ANIK AHMET,ÇATLI GÖNÜL,BERBEROĞLU MERİH, "Çok Merkezli Olarak Hipofosfatemik Riketsli Olguların Değerlendirilmesi", XXII.ULUSAL PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, ANTALYA
5. GÜRAN TÜLAY,Tezel Başak,GÜRBÜZ FATİH,SELVER EKLİOĞLU BERAY,HATİPOĞLU NİHAL,KARA CENGİZ,ŞİMŞEK ENVER,Şahin Nuran,ÇİZMECİOĞLU FİLİZ MİNE,Özon Alev,BAŞ FİRDEVS,Özdemir Gülsüm,Aydın Murat,DARENDELİLER FATMA FEYZA, "Türkiyede Konjenital Adrenal Hiperplazi Yenidoğan Taraması", XXII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi
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2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
BİLDİRİ
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş
2018
YAYINLAR
MAKALE
Belirtilmemiş