Prof.Dr. SERAP DEMİRCİOĞLU
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. Özdemir Hülya,MEMİŞOĞLU ASLI,Alp Ünkar Zeynep,ARCAGÖK BARAN CENGİZ,BİLGEN HÜLYA SELVA,TURAN SERAP,ÖZEK EREN. Persistent hyperglycemia in a neonate: is it a complication of therapeutic hypothermia?. The Turkish Journal of Pediatrics. Cilt 59. sf 193-, 2017. (Yayına Ulaşmak İçin Tıklayınız)
2. EREN ERDAL,Törel Ergür Ayça,İŞGÜVEN ŞÜKRİYE PINAR,BERBEROĞLU MERİH,ŞIKLAR ZEYNEP,BAŞ FİRDEVS,YEL SERVET,BAŞ SERPİL,SÖBÜ ELİF,BEREKET ABDULLAH,DEMİRCİOĞLU SERAP,SAĞLAM HALİL,ATAY ZEYNEP,ERCAN OYA,GÜRAN TÜLAY,ATABEK MEHMET EMRE,Korkmaz Hüseyin Anıl,Kılınç Uğurlu Aylin,AKINCI AYŞEHAN,DÖĞER ESRA,ŞİMŞEK ENVER,Akbaş Emine Demet,ABACI AYHAN,Gül Ülkü,Acar Sezer,Mengen Uçaktürk Eda,YILDIZ MELEK,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)
3. HALİLOĞLU BELMA,ABALI SAYGIN,BUĞRUL FUAT,Çelik Enes,BAŞ SERPİL,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. Sunter Gulin,Enver Ece Oge,Akbarzade Azad,DEMİRCİOĞLU SERAP,Vatansever Pinar,Gunal Dilek Ince,HAKLAR GONCAGÜL,BEREKET ABDULLAH,AGAN Kadriye,GÜRAN TÜLAY. Acquired modification of sphingosine-1-phosphate lyase activity is not related to adrenal insufficiency. BMC Neurology. Cilt 18. sf 48-48, 2018. (Yayına Ulaşmak İçin Tıklayınız)
5. POYRAZOĞLU ŞÜKRAN,BUNDAK RÜVEYDE,YAVAŞ ABALI ZEHRA,ÖNAL HASAN,AKGÜN ABDURRAHMAN,BAŞ SERPİL,ABALI SAYGIN,BEREKET ABDULLAH,EREN ERDAL,TARIM ÖMER FARUK,GÜVEN AYLA,YILDIZ METİN,KARAMAN AKSAKAL DERYA,YÜKSEL AYŞEGÜL,SEYMEN KARABULUT GÜLCAN,HATUN ŞÜKRÜ,ÖZGEN İLKER TOLGA,CESUR YAŞAR,DİLEK EMİNE,TÜTÜNCÜLER FİLİZ,ÇAKIIR ESRA PAPATYA,Özcabı Bahar,EVLİYAOĞLU SAADET OLCAY,Karadeniz Songül,Dursun Fatma,BOLU SEMİH,ARSLANOĞLU İLKNUR,YEŞİLTEPE MUTLU RAHİME GÜL,Kırmızıbekmez Heves,İŞGÜVEN ŞÜKRİYE PINAR,ÜSTYOL ALA,ADAL SERVET ERDAL,Uçar Ahmet,CEBECİ AYŞE NURCAN,Binay Çigdem,SEMİZ SERAP,Korkmaz Hüseyin Anıl,Memioğlu Nihal,Sagsak Elif,PELTEK KENDİRCİ HAVVA NUR,YILDIZ MELEK,Akçay Teoman,DEMİRCİOĞLU SERAP,GÜRAN TÜLAY,ATAY ZEYNEP,AKCAN 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)
6. TURAN SERAP. Current Nomenclature of Pseudohypoparathyroidism: Inactivating Parathyroid Hormone/Parathyroid Hormone-Related Protein Signaling Disorder. Journal of Clinical Research in Pediatric Endocrinology. Cilt 9. sf 58-68, 2018. (Yayına Ulaşmak İçin Tıklayınız)
7. BEREKET ABDULLAH,YEŞİLKAYA EDİZ,DARENDELİLER FATMA FEYZA,BAŞ FİRDEVS,DARCAN ŞÜKRAN,ADAL SERVET ERDAL,AKINCI AYŞEHAN,ATABEK MEHMET EMRE,DEMİREL FATMA,ÖZKAN BEHZAT,ÖZHAN BAYRAM,ORBAK ZERRİN,ERSOY BETÜL,TURAN SERAP,GÖKŞEN ŞİMŞEK RUHSAR DAMLA,TARIM ÖMER FARUK,YÜKSEL BİLGİN,ERCAN OYA,HATUN ŞÜKRÜ,ŞİMŞEK ENVER,ABACI AYHAN,DÖNERAY HAKAN,KESKİN MEHMET,DEMİR KORCAN,TOPALOĞLU ALİ KEMAL,EREN ERDAL,ÖZEN SAMİM,AKIN LEYLA,SAĞLAM HALİL,ÖZGEN İLKER TOLGA,ŞEN YAŞAR,ANDIRAN NESİBE,ÇİZMECİOĞLU FİLİZ MİNE,EVLİYAOĞLU SAADET OLCAY,KARAGÜZEL GÜLAY,PİRGON MUSTAFA ÖZGÜR,DEMİRBİLEK HÜSEYİN,CİNAZ PEYAMİ. Turner Syndrome and Associated Problems in Turkish Children A Multicenter Study. Journal of Clinical Research in Pediatric Endocrinology. Cilt 7. sf 27-36, 2015. (Yayına Ulaşmak İçin Tıklayınız)
8. ÖZTÜRK MAKBULE NİLÜFER,CİNEL İSMAİL HAKKI,YAMAN ALİ,HAKLAR GONCAGÜL,ŞİRİKÇİ ÖNDER,TURAN SERAP,ALTINKANAT GELMEZ GÜLŞEN. The diagnostic value of soluble urokinase plasminogen activator receptor suPAR compared to C reactive protein CRP and procalcitonin PCT in children with systemic inflammatory response syndrome SIRS. Journal of Infection and Chemotherapy. Cilt 23. sf 17-22, 2017. (Yayına Ulaşmak İçin Tıklayınız)
9. 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)
10. Belma Haliloglu,Atay Zeynep,GÜRAN TÜLAY,ABALI SAYGIN,Serpil Bas,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)
11. CİNEL İSMAİL HAKKI,KOÇ AHMET,TOKUÇ AYŞE GÜLNUR,YAMAN ALİ,HAKLAR GONCAGÜL,ŞİRİKÇİ ÖNDER,TURAN SERAP,ALTINKANAT GELMEZ GÜLŞEN. The diagnostic value of soluble urokinase plasminogen activator receptor compared with C reactive protein and procalcitonin in children with febrile neutropenia. Pediatric Hematology and Oncology. Cilt 33. sf 200-208, 2016. (Yayına Ulaşmak İçin Tıklayınız)
12. ŞIKLAR ZEYNEP,POYRAZOĞLU ŞÜKRAN,BAŞ FİRDEVS,DARENDELİLER FATMA FEYZA,BUNDAK RÜVEYDE,AYCAN ZEHRA,GÜVEN AYLA,ABALI SAYGIN,ATAY ZEYNEP,TURAN SERAP,KARA CENGİZ,ABACI AYHAN,BOLU SEMİH,ŞİMŞEK ENVER,ÇATLI GÖNÜL,EVLİYAOĞLU SAADET OLCAY,İŞGÜVEN ŞÜKRİYE PINAR,ÖZGEN İLKER TOLGA,HATİPOĞLU NİHAL,ELHAN ATİLLA HALİL,BERBEROĞLU MERİH. The Growth Characteristics of Patients with Noonan Syndrome Results of Three Years of Growth Hormone Treatment A Nationwide Multicenter Study. Journal of Clinical Research in Pediatric Endocrinology. Cilt 8. sf 305-312, 2016. (Yayına Ulaşmak İçin Tıklayınız)
13. 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)
14. Mantovani Giovanna,Bastepe Murat,Monk David,de Sanctis Luisa,Thiele Susanne,Usardi Alessia,Ahmed S Faisal,Bufo Roberto,Choplin Timothée,De Filippo Gianpaolo,Devernois Guillemette,Eggermann Thomas,Elli Francesca M,Freson Kathleen,García Ramirez Aurora,Germain-Lee Emily L,Groussin Lionel,Hamdy Neveen,Hanna Patrick,Hiort Olaf,Jüppner Harald,Peter Kamenický,Knight Nina,Kottler Marie-Laure,Le Norcy Elvire,Lecumberri Beatriz,Levine Michael A,Mäkitie Outi,Martin Regina,Martos-Moreno Gabriel Ángel,Minagawa Masanori,Murray Philip,Pereda Arrate,Pignolo Robert,Rejnmark Lars,Rodado Rebecca,Rothenbuhler Anya,Saraff Vrinda,Shoemaker Ashley H,Shore Eileen M,Silve Caroline,DEMİRCİOĞLU SERAP,Woods Philip,Zillikens M Carola,Perez de Nanclares,Linglart Agnès. Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement. Nature Reviews Endocrinology. Cilt 14. sf 476-500, 2018. (Yayına Ulaşmak İçin Tıklayınız)
15. 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)
16. Akesen Eda,TURAN SERAP,GÜRAN TÜLAY,Atay Zeynep,SAVE DİLŞAD,BEREKET ABDULLAH. Prevalence of type 1 diabetes mellitus in 6-18-yr-old school children living in Istanbul, Turkey. Pediatric Diabetes. Cilt 12. sf 567-571, 2011. (Yayına Ulaşmak İçin Tıklayınız)
17. Thiele Susanne,Mantovani Giovanna,Barlier Anne,Boldrin Valentina,Bordoga Paolo,De Sanctis Luisa,Elli Francesca M,Freson Kathleen,Garin Intza,Grybek Virginie,Hanna Patrick,Izzi Benedetta,Hiort Olaf,Lecumberri Beatriz,Pereda Arrate,Saraff Vrinda,Silve Caroline,TURAN SERAP,Usardi Alessia,Werner Ralf,de Nanclares Guiomar Perez,Linglart Agns. From pseudohypoparathyroidism to inactivating PTH PTHrP signalling disorder iPPSD a novel classification proposed by the EuroPHP network. European Journal of Endocrinology. Cilt 175. sf 1-17, 2016. (Yayına Ulaşmak İçin Tıklayınız)
18. Brömme Dieter,Panwar Preety,TURAN SERAP. Cathepsin K osteoporosis trials pycnodysostosis and mouse deficiency models Commonalities and differences. Expert Opinion on Drug Discovery. Cilt 11. sf 457-472, 2016. (Yayına Ulaşmak İçin Tıklayınız)
19. Baglam Tekin,Binnetoglu Adem,Fatih Topuz Muhammet,Baş Ikizoglu Nilay,Ersu Refika,TURAN SERAP,Sarı Murat. Pycnodysostosis at otorhinolaryngology. International Journal of Pediatric Otorhinolaryngology. Cilt 95. sf 91-96, 2017. (Yayına Ulaşmak İçin Tıklayınız)
20. Bastepe Murat,TURAN SERAP,He Qing. Heterotrimeric G proteins in the control of parathyroid hormone actions. Journal of Molecular Endocrinology. Cilt 58. sf 203-224, 2017. (Yayına Ulaşmak İçin Tıklayınız)
21. 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.
22. TURAN SERAP,Aydin Cumhur,BEREKET ABDULLAH,Akcay Teoman,GÜRAN TÜLAY,Akcay Teoman,Yaralioglu Betul Akmen,Bastepe Murat,Jüppner Harald. 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)
23. Chillambhi Smitha,TURAN SERAP,Hwang Daw-Yang,Chen Hung-Chun,Jüppner Harald,Bastepe Murat. Deletion of the Noncoding GNAS Antisense Transcript Causes Pseudohypoparathyroidism Type Ib and Biparental Defects of GNAS Methylation in cis. The Journal of Clinical Endocrinology & Metabolism. Cilt 95. sf 3993-4002, 2010. (Yayına Ulaşmak İçin Tıklayınız)
24. POYRAZOĞLU ŞÜKRAN,ATABEK MEHMET EMRE,ŞİMŞEK ENVER,ÖZGEN İLKER TOLGA,KESKİN MEHMET,KARA CENGİZ,GÜVEN AYLA,DEMİR KORCAN,DARCAN ŞÜKRAN,CESUR YAŞAR,BÖBER ECE,BİRCAN İFFET,ŞIKLAR ZEYNEP,YÜKSEL BİLGİN,ERSOY BETÜL,BERBEROĞLU MERİH,KURTOĞLU SELİM,BİDECİ AYSUN,BEREKET ABDULLAH,YEŞİLKAYA EDİZ,TURAN SERAP,Özbek Mehmet Nuri,Memioglu Nihal,Sarı Erkan,Can Şule,ESEN İHSAN,DARENDELİLER FATMA FEYZA. Current Practice in Diagnosis and Treatment of Growth Hormone Deficiency in Childhood A Survey from Turkey. Journal of Clinical Research in Pediatric Endocrinology. Cilt 7. sf 37-44, 2015. (Yayına Ulaşmak İçin Tıklayınız)
25. ATAY ZEYNEP,TURAN SERAP,AKIN LEYLA,EREN ERDAL,DÖĞER ESRA,AYCAN ZEHRA,YAVAŞ ABALI ZEHRA,AKINCI AYŞEHAN,ŞIKLAR ZEYNEP,ÖZEN SAMİM,YEŞİLKAYA EDİZ,KARA CENGİZ,TÜTÜNCÜLER FİLİZ,KARAGÜZEL GÜLAY,Erdeve Senay Savas,SAĞLAM HALİL,BİDECİ AYSUN,Sarı Erkan,SEYMEN KARABULUT GÜLCAN,Çetinkaya Semra,Tayfun Meltem,KURTOĞLU SELİM,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)
26. GÜRAN TÜLAY,AYCAN ZEHRA,BEREKET ABDULLAH,BAŞ FİRDEVS,DARCAN ŞÜKRAN,BİDECİ AYSUN,GÜVEN AYLA,DEMİR KORCAN,Ozbek Mehmet Nuri,AKINCI AYŞEHAN,Buyukinan Muammer,Aydin Banu Kucukemre,TURAN SERAP,Agladioglu Sebahat Yilmaz,Atay Zeynep,Abali Zehra Yavas,TARIM ÖMER FARUK,Catli Gonul,YÜKSEL BİLGİN,Akcay Teoman,Yildiz Metin,ÖZEN SAMİM,Doger Esra,DEMİRBİLEK HÜSEYİN,Ucar Ahmet,Isik Emregul,ÖZHAN BAYRAM,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)
27. Haliloğlu Belma,ATAY ZEYNEP,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)
28. Aydıner Ömer,Aydıner Karakoç Elif,AKPINAR İHSAN NURİ,TURAN SERAP,BEREKET ABDULLAH. Normative Data of Thyroid Volume Ultrasonographic Evaluation of 422 Subjects Aged 0 55 Years. Journal of Clinical Research in Pediatric Endocrinology. Cilt 7. sf 98-101, 2015. (Yayına Ulaşmak İçin Tıklayınız)
29. BAYRAM YAVUZ,ABACI AYHAN,TURAN SERAP,BÖBER ECE,BEREKET ABDULLAH,Gulsuner Suleyman,Yesil Gozde,Gulsuner Hilal Unal,Atay Zeynep,Pierce Sarah B,Tomasz Gambin,Lee Ming,Atik Mehmed M,Walsh Tom,Karaca Ender,PEHLİVAN DAVUT,Jhangiani Shalini N,Donna Muzny,Buyukgebiz Atilla,Boerwinkle Eric,Gibbs Richard A,King Mary-Claire,Lupski James R. Homozygous Loss of function Mutations in SOHLH1 in Patients With Nonsyndromic Hypergonadotropic Hypogonadism. The Journal of Clinical Endocrinology & Metabolism. Cilt 100. sf 808-814, 2015. (Yayına Ulaşmak İçin Tıklayınız)
30. AKALIN FİGEN,GÜLAY ALPER,ÖZTUNÇ FİGEN,KOTİLOĞLU ESİN,TURAN SERAP. A case of glycogen storage disease type II with double aortic arch. Acta Paediatr. Cilt 89. sf 884-6, 2000.
31. BEREKET ABDULLAH,TURAN SERAP,GÜLAY ALPER,ÇOMU SİNAN,ALPAY HARİKA,AKALIN FİGEN. Two patients with Kabuki syndrome presenting with endocrine problems. J Pediatr Endocrinol Metab.. Cilt 14. sf 215-20, 2001.
32. ÖZKAN BEHZAT,BEREKET ABDULLAH,TURAN SERAP,Keskin Sabiha. Addition of orlistat to conventional treatment in adolescents with severe obesity. European Journal of Pediatrics. Cilt 163. sf 738-741, 2004. (Yayına Ulaşmak İçin Tıklayınız)
33. AKALIN FİGEN,TURAN SERAP,GÜRAN TÜLAY,AYABAKAN CANAN. Increased QT dispersion in breath holding spells. Acta Paediatr. Cilt 93. sf 770-4, 2004.
34. BEREKET ABDULLAH,TURAN SERAP,Karaman M Goksin,HAKLAR GONCAGÜL,Ozbay Fatih,Yazgan M Yanki. Height Weight IGF I IGFBP 3 and Thyroid Functions in Prepubertal Children with Attention Deficit Hyperactivity Disorder Effect of Methylphenidate Treatment. Hormone Research. Cilt 63. sf 159-164, 2005. (Yayına Ulaşmak İçin Tıklayınız)
35. TURAN SERAP,BEREKET ABDULLAH,Omar Anjumara,Berber Mustafa,ÖZEN AHMET OĞUZHAN. Upper segment lower segment ratio and armspan height difference in healthy Turkish children. Acta Paediatr. Cilt 94. sf 407-13, 2005.
36. Çam Sabahat,BEREKET ABDULLAH,TURAN SERAP,Taga Yavuz,HAKLAR GONCAGÜL. Effect of zinc supplementation on growth hormone secretion IGF I IGFBP 3 somatomedin generation alkaline phosphatase osteocalcin and growth in prepubertal children with idiopathic short stature. J Pediatr Endocrinol Metab.. Cilt 18. sf 69-74, 2005.
37. TURAN SERAP,Saka Nurcin,GÜNEY AHMET İLTER,BEREKET ABDULLAH. A Patient with Hypopituitarism and Isochromosome 18q Mosaicism. Hormone Research. Cilt 64. sf 261-265, 2005. (Yayına Ulaşmak İçin Tıklayınız)
38. BEREKET ABDULLAH,TURAN SERAP,Omar Anjumanara,Berber Mustafa,Ozen Ahmet,Akbenlioglu Cengiz,HAKLAR GONCAGÜL. Serum IGF I and IGFBP 3 Levels of Turkish Children during Childhood and Adolescence Establishment of Reference Ranges with Emphasis on Puberty. Hormone Research. Cilt 65. sf 96-105, 2006. (Yayına Ulaşmak İçin Tıklayınız)
39. TURAN SERAP,BEREKET ABDULLAH,FURMAN ANDRZEJ,Anjumara Omar,Berber Mustafa,Ozen Ahmet,Akbenlioglu Cengiz. The effect of economic status on height insulin like growth factor IGF I and IGF binding protein 3 concentrations in healthy Turkish children. European Journal of Clinical Nutrition. Cilt 61. sf 752-758, 2006. (Yayına Ulaşmak İçin Tıklayınız)
40. TURAN SERAP,GÜRAN TÜLAY,Topcu Burcu,Akcay Teoman,BEREKET ABDULLAH. Severe diabetic ketoacidosis hyperventilation or relative hypoventilation. Pediatric Critical Care Medicine. Cilt 7. sf 291-, 2006. (Yayına Ulaşmak İçin Tıklayınız)
41. Semerci C Nur,Satiroglu-Tufan N Lale,TURAN SERAP,BEREKET ABDULLAH,Tuysuz Beyhan,Yilmaz Elif,KAYSERİLİ KARABEY HÜLYA,KARAMAN BİRSEN,SEMİZ SERAP,DÜZCAN FÜSUN,BAĞCI HÜSEYİN. Detection of Y Chromosomal Material in Patients with a 45 X Karyotype by PCR Method. The Tohoku Journal of Experimental Medicine. Cilt 211. sf 243-249, 2007. (Yayına Ulaşmak İçin Tıklayınız)
42. GÜRAN TÜLAY,TURAN SERAP,KARADAĞ BÜLENT TANER,Ersu Refika,Fazilet Karakoç,BEREKET ABDULLAH,DAĞLI ELİF. Bone mineral density in children with non cystic fibrosis bronchiectasis. Respiration. Cilt 75. sf 432-6, 2007.
43. TURAN SERAP,BEREKET ABDULLAH,Angaji Meryem,Köroğlu Özge Altun,BİLGEN HÜLYA SELVA,Onver Tamer,AKMAN İPEK,ÖZEK EREN. The effect of the mode of delivery on neonatal thyroid function. Journal of Maternal-Fetal and Neonatal Medicine. Cilt 20. sf 473-476, 2007. (Yayına Ulaşmak İçin Tıklayınız)
44. TURAN SERAP,GÜRAN TÜLAY,BEREKET ABDULLAH,Akçay Teoman. Alendronate treatment in children with osteogenesis imperfecta. Indian Pediatr. Cilt 45. sf 105-9, 2008.
45. TURAN SERAP,Omar Anjumanara,BEREKET ABDULLAH. Comparison of capillary blood ketone measurement by electrochemical method and urinary ketone in treatment of diabetic ketosis and ketoacidosis in children. Acta Diabetologica. Cilt 45. sf 83-85, 2008. (Yayına Ulaşmak İçin Tıklayınız)
46. POYRAZOĞLU ŞÜKRAN,BAŞ FİRDEVS,TURAN SERAP,BEREKET ABDULLAH,DARENDELİLER FATMA FEYZA,Saka Nurcin,Dogu A,İŞGÜVEN ŞÜKRİYE PINAR,ADAL SERVET ERDAL,ÇİZMECİOĞLU FİLİZ MİNE,SAĞLAM HALİL,ERCAN OYA,HATUN ŞÜKRÜ,BUNDAK RÜVEYDE,AKIN LEYLA,Akçay Teoman,Yıldız metin,Memioğlu Nihal,Sarikaya Sevil. Evaluation of diagnosis and treatment results in children with Graves disease with emphasis on the pubertal status of patients. J Pediatr Endocrinol Metab. Cilt 21. sf 745-51, 2008.
47. 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)
48. Elif Karakoc,TURAN SERAP,AKPINAR İHSAN NURİ,İŞGÜVEN ŞÜKRİYE PINAR,ADAL SERVET ERDAL,HAKLAR GONCAGÜL,DEDE FUAT,BEREKET ABDULLAH. Screening of Parents and Siblings of Patients with Thyroid Dysgenesis by Thyroid Function Tests and Ultrasound. Hormone Research. Cilt 70. sf 329-339, 2008. (Yayına Ulaşmak İçin Tıklayınız)
49. TURAN SERAP,BEREKET ABDULLAH,GÜRAN TÜLAY,Akcay Teoman,Papari-Zareei M,Auchus R J. 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)
50. BEREKET ABDULLAH,TURAN SERAP,BUNDAK RÜVEYDE,DARENDELİLER FATMA FEYZA,DARCAN ŞÜKRAN. Adult height in Turkish patients with Turner syndrome without growth hormone treatment. Turk J Pediatr. Cilt 50. sf 415-7, 2008.
51. GÜRAN TÜLAY,TURAN SERAP,BEREKET ABDULLAH,BAŞ FİRDEVS,BUNDAK RÜVEYDE,DARENDELİLER FATMA FEYZA,Akcay Teoman,Akcay Teoman,Unluguzel Goksenin,Gunoz Hulya,Saka Nurcin,İŞGÜVEN ŞÜKRİYE PINAR,ADAL SERVET ERDAL,Yildiz Metin,Sarikaya Sevil,AKIN LEYLA,Memioglu Nihal,Onal Hasan,ERCAN OYA,HAKLAR GONCAGÜL. 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)
52. GÜRAN TÜLAY,BİRCAN RIFAT,TURAN SERAP,BEREKET ABDULLAH. Alopecia association with resistance to thyroid hormones. J Pediatr Endocrinol Metab.. Cilt 22. sf 1075-81, 2009.
53. GÜRAN TÜLAY,BEREKET ABDULLAH,TURAN SERAP,TOPALOĞLU ALİ 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)
54. TURAN SERAP,Fernandez-Rebollo Eduardo,Aydin Cumhur,Zoto Teuta,Reyes Monica,Bounoutas George,Chen Min,Weinstein Lee S. Postnatal Establishment of Allelic G s Silencing as a Plausible Explanation for Delayed Onset of Parathyroid Hormone Resistance Owing to Heterozygous G s Disruption. Journal of Bone and Mineral Research. Cilt 29. sf 749-760, 2014. (Yayına Ulaşmak İçin Tıklayınız)
55. GÜRAN TÜLAY,TURAN SERAP,BİRCAN 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. J Pediatr Endocrinol Metab. Cilt 22. sf 971-8, 2009.
56. GÜRAN TÜLAY,TURAN SERAP,ÖZKAN BEHZAT,BEREKET ABDULLAH. Cushing s syndrome due to a non adrenal ectopic adrenocorticotropin secreting Ewing s sarcoma in a child. J Pediatr Endocrinol Metab. Cilt 22. sf 363-8, 2009.
57. Akcay Teoman,TURAN SERAP,GÜRAN TÜLAY,Unluguzel Goksenin,HAKLAR GONCAGÜL,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)
58. Mäkitie Outi,Pereira Renata C,Ilkka Kaitila,TURAN SERAP,Bastepe Murat,Laine Tero,Kröger Heikki,William G Cole. Long term clinical outcome and carrier phenotype in autosomal recessive hypophosphatemia caused by a novel DMP1 mutation. Journal of Bone and Mineral Research. Cilt 25. sf 2165-2174, 2010. (Yayına Ulaşmak İçin Tıklayınız)
59. GÜRAN TÜLAY,TURAN SERAP,Akcay Teoman,Degirmenci Fatih,Avci Okan,Asan Abdulkerim,Erdil Emre,Majid Abdulaziz,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)
60. GÜRAN TÜLAY,EKİNCİ GAZANFER,Atay Zeynep,TURAN SERAP,Akcay Teoman,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)
61. Fernández-Rebollo Eduardo,de Nanclares Pérez,Lecumberri Beatriz,TURAN SERAP,Anda Emma,Pérez-Nanclares Gustavo,Feig Denice,Nik-Zainal Serena. Exclusion of the GNAS locus in PHP Ib patients with broad GNAS methylation changes Evidence for an autosomal recessive form of PHP Ib. Journal of Bone and Mineral Research. Cilt 26. sf 1854-1863, 2011. (Yayına Ulaşmak İçin Tıklayınız)
62. TURAN SERAP,AKIN LEYLA,Akcay T,ADAL SERVET ERDAL,Sarikaya S,Bastepe M,Juppner H. Recessive versus imprinted disorder consanguinity can impede establishing the diagnosis of autosomal dominant pseudohypoparathyroidism type Ib. European Journal of Endocrinology. Cilt 163. sf 489-493, 2010. (Yayına Ulaşmak İçin Tıklayınız)
63. BEREKET ABDULLAH,CESUR YAŞAR,ÖZKAN BEHZAT,ADAL SERVET ERDAL,TURAN SERAP,Hanedan Onan Sertac,DÖNERAY HAKAN,Akcay Teoman,HAKLAR GONCAGÜL. Circulating Insulin like Growth Factor Binding Protein 4. Journal of Clinical Research in Pediatric Endocrinology. Cilt 2. sf 17-20, 2010. (Yayına Ulaşmak İçin Tıklayınız)
64. TURAN SERAP,Topcu Burcu,Gökce İbrahim,GÜRAN TÜLAY,Atay Zeynep,Omar Anjumanara,Akçay Teoman,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)
65. GÜRAN TÜLAY,ARMAN AYŞE,AKÇAY TEOMAN,KAYAN E,ATAY ZEYNEP,TURAN SERAP,BEREKET ABDULLAH. Cognitive and psychosocial development in children with familial hypomagnesaemia. Magnes Res.. Cilt 24. sf 7-12, 2011.
66. TURAN SERAP,ÖZDEMİR GÜL NİHAL,GÜRAN TÜLAY,AKALIN FİGEN,Akçay Teoman,AYABAKAN CANAN,Yılmaz Yüksel,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)
67. AYDINER KARAKOÇ ELİF,TURAN SERAP,AKPINAR İHSAN NURİ,DEDE FUAT,İŞGÜVEN ŞÜKRİYE PINAR,ADAL SERVET 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)
68. ATAY ZEYNEP,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)
69. Liu Z,TURAN SERAP,Wehbi V L,Vilardaga J-P,Bastepe M. Extra long G s Variant XL s Protein Escapes Activation induced Subcellular Redistribution and Is Able to Provide Sustained Signaling. Journal of Biological Chemistry. Cilt 286. sf 38558-38569, 2011. (Yayına Ulaşmak İçin Tıklayınız)
70. GÜRAN TÜLAY,Akcay T,BEREKET ABDULLAH,Atay Z,TURAN SERAP,Haisch L,Konrad M,Schlingmann K P. 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)
71. BAŞ FİRDEVS,DARENDELİLER FATMA FEYZA,AYCAN ZEHRA,BERBEROĞLU MERİH,ŞIKLAR ZEYNEP,DARCAN ŞÜKRAN,GÖKŞEN ŞİMŞEK RUHSAR DAMLA,BİDECİ AYSUN,CİNAZ PEYAMİ,BÖBER ECE,DEMİR KORCAN,BEREKET ABDULLAH,TURAN SERAP,ATABEK MEHMET EMRE,TÜTÜNCÜLER FİLİZ,BUNDAK RÜVEYDE. The Exon 3 Deleted Full Length Growth Hormone Receptor Polymorphism and Response to Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome A Multicenter Study. Hormone Research in Paediatrics. Cilt 77. sf 85-93, 2012. (Yayına Ulaşmak İçin Tıklayınız)
72. 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)
73. Fernandez-Rebollo E,Maeda A,Reyes M,TURAN SERAP,Frohlich L F,Plagge A,Kelsey G,Juppner H. Loss of XL s extra large s imprinting results in early postnatal hypoglycemia and lethality in a mouse model of pseudohypoparathyroidism Ib. Proceedings of the National Academy of Sciences. Cilt 109. sf 6638-6643, 2012. (Yayına Ulaşmak İçin Tıklayınız)
74. TURAN SERAP,Jaakko Ignatius,Moilanen Jukka S,Kuismin Outi,Stewart Helen,Mann Nicholas P,Linglart Agnès,Bastepe Murat,Jüppner Harald. De Novo STX16 Deletions An Infrequent Cause of Pseudohypoparathyroidism Type Ib that Should Be Excluded in Sporadic Cases. The Journal of Clinical Endocrinology & Metabolism. Cilt 97. sf 2314-2319, 2012. (Yayına Ulaşmak İçin Tıklayınız)
75. Atay Zeynep,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)
76. Atay Zeynep,TURAN SERAP,BEREKET ABDULLAH,Haliloglu Belma,MEMİŞOĞLU ASLI,Khayat Morad,Shalev Stavit A,Spiegel Ronen. A novel homozygous TMEM70 mutation results in congenital cataract and neonatal mitochondrial encephalo cardiomyopathy. Gene. Cilt 515. sf 197-199, 2013. (Yayına Ulaşmak İçin Tıklayınız)
77. Ozdemir Hulya,AKMAN İPEK,Coskun Senay,Demirel Utku,TURAN SERAP,BEREKET ABDULLAH,BİLGEN HÜLYA SELVA,ÖZEK EREN. Maternal Thyroid Dysfunction and Neonatal Thyroid Problems. International Journal of Endocrinology. Cilt 2013. sf 1-6, 2013. (Yayına Ulaşmak İçin Tıklayınız)
78. Haliloglu Belma,GÜRAN TÜLAY,Atay Zeynep,ABALI SAYGIN,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)
79. TURAN SERAP,Bastepe Murat. The GNAS Complex Locus and Human Diseases Associated with Loss of Function Mutations or Epimutations within This Imprinted Gene. Hormone Research in Paediatrics. Cilt 80. sf 229-241, 2013. (Yayına Ulaşmak İçin Tıklayınız)
80. TURAN SERAP,Bastepe Murat. GNAS Spectrum of Disorders. Current Osteoporosis Reports. Cilt 13. sf 146-158, 2015. (Yayına Ulaşmak İçin Tıklayınız)
81. BEREKET ABDULLAH,BAŞ FİRDEVS,BUNDAK RÜVEYDE,DARCAN ŞÜKRAN,DÜNDAR BUMİN NURİ,KARA CENGİZ,ADAL SERVET ERDAL,AKINCI AYŞEHAN,ATABEK MEHMET EMRE,DEMİREL FATMA,ÖZKAN BEHZAT,ÖZHAN BAYRAM,ORBAK ZERRİN,ERSOY BETÜL,Doğan Murat,ATAŞ ALİ,TURAN SERAP,GÖKŞEN ŞİMŞEK RUHSAR DAMLA,TARIM ÖMER FARUK,YÜKSEL BİLGİN,ERCAN OYA,HATUN ŞÜKRÜ,ŞİMŞEK ENVER,ABACI AYHAN,DÖNERAY HAKAN,KESKİN MEHMET,TOPALOĞLU ALİ KEMAL,EREN ERDAL,DEMİRBİLEK HÜSEYİN,ABALI SAYGIN,AKIN LEYLA,KABA SULTAN,ANIK AHMET,BAŞ SERPİL,ÇİZMECİOĞLU FİLİZ MİNE,EVLİYAOĞLU SAADET OLCAY,KARAGÜZEL GÜLAY,PİRGON MUSTAFA ÖZGÜR,ÇATLI GÖNÜL,GÜRBÜZ FATİH,CİNAZ PEYAMİ,DARENDELİLER FATMA FEYZA. Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome. American Journal of Medical Genetics Part A. Cilt 170. sf 942-948, 2016. (Yayına Ulaşmak İçin Tıklayınız)
82. TUĞTEPE HALİL,Thomas David Terence,TURAN SERAP,ÇİZMECİOĞLU FİLİZ MİNE,HATUN ŞÜKRÜ,BEREKET ABDULLAH,DAĞLI EMRULLAH TOLGA. Does common channel length affect surgical choice in female congenital adrenal hyperplasia patients. Journal of Pediatric Urology. Cilt 10. sf 948-954, 2014. (Yayına Ulaşmak İçin Tıklayınız)
83. TURAN SERAP,Erdoğan Hilal Kaya,Altunay İlknur Kıvanç. Prevalence of acne in primary school children and the relationship of acne with pubertal maturation. TURKDERM. Cilt 48. sf 182-186, 2014. (Yayına Ulaşmak İçin Tıklayınız)
84. Kühnen Peter,TURAN SERAP,Fröhler Sebastian,GÜRAN TÜLAY,ABALI SAYGIN,Biebermann Heike,BEREKET ABDULLAH,Grüters Annette. 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)
85. Atay Zeynep,BEREKET ABDULLAH,Belma Haliloglu,ABALI SAYGIN,Ozdogan Tutku,Altuncu Emel,Canaff Lucie,Vilaça Tatiane,Wong Betty YL,Cole David EC,Geoffrey N Hendy,TURAN SERAP. Novel homozygous inactivating mutation of the calcium sensing receptor gene CASR in neonatal severe hyperparathyroidism lack of effect of cinacalcet. Bone. Cilt 64. sf 102-107, 2014. (Yayına Ulaşmak İçin Tıklayınız)
86. ARMAN AHMET,BEREKET ABDULLAH,Coker Ajda,ŞİMŞEK KİPER PELİN ÖZLEM,GÜRAN TÜLAY,ÖZKAN BEHZAT,Atay Zeynep,AKÇAY TEOMAN,HALİLOĞLU BELMA,BODUROĞLU OSMAN 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)
87. TURAN SERAP. Current research on pycnodysostosis. Intractable & Rare Diseases Research. Cilt 3. sf 91-93, 2014. (Yayına Ulaşmak İçin Tıklayınız)
88. Kirac Deniz,GÜNEY AHMET İLTER,Akcay Teoman,GÜRAN TÜLAY,ULUCAN KORKUT,TURAN SERAP,Ergec Deniz,Koc Gulsah,Eren Fatih,Kaspar Elif Cigdem,Elif Cigdem Kaspar,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)
89. Akcay Teoman,Fernandez-Cancio M,TURAN SERAP,GÜRAN TÜLAY,Audi Laura,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)
90. Garin Intza,Mantovani Giovanna,Aguirre Urko,Barlier Anne,Brix Bettina,Elli Francesca M,Freson Kathleen,Virginie Grybek,TURAN SERAP. European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS an EQA study. European Journal of Human Genetics. Cilt 23. sf 438-444, 2014. (Yayına Ulaşmak İçin Tıklayınız)
91. 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)
92. TURAN SERAP,Thiele Susanne,Tafaj Olta,Brix Bettina,Atay Zeynep,ABALI SAYGIN,Haliloglu Belma,BEREKET ABDULLAH. Evidence of hormone resistance in a pseudo pseudohypoparathyroidism patient with a novel paternal mutation in GNAS. Bone. Cilt 71. sf 53-57, 2015. (Yayına Ulaşmak İçin Tıklayınız)
93. 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)
94. 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)
95. DARENDELİLER FATMA FEYZA,BEREKET ABDULLAH,BUNDAK RÜVEYDE,DARCAN ŞÜKRAN,KARA CENGİZ,DÜNDAR BUMİN NURİ,ADAL SERVET ERDAL,ATABEK MEHMET EMRE,DEMİREL FATMA,ÖZKAN BEHZAT,ÖZHAN BAYRAM,ORBAK ZERRİN,ERSOY BETÜL,TURAN SERAP,GÖKŞEN ŞİMŞEK RUHSAR DAMLA,TARIM ÖMER FARUK,YÜKSEL BİLGİN,ERCAN OYA,HATUN ŞÜKRÜ,ŞİMŞEK ENVER,ABACI AYHAN,DÖNERAY HAKAN,KESKİN MEHMET,DEMİR KORCAN,TOPALOĞLU ALİ KEMAL,EREN ERDAL,ÖZEN SAMİM,DEMİRBİLEK HÜSEYİN,AKIN LEYLA,SAĞLAM HALİL,Yeşilkaya Ediz,Sarı Erkan,Küçükemre Aydın Banu,Büyükinan Muammer,Mazıcıoğlu Mümtaz M,Çelik Nurullah,Doğan Murat,ATAŞ ALİ,Ayşenur Ökten,Özbek Mehmet Nuri,Önal Hasan,Akyürek Nesibe,Bulan Kezban,Tepe Derya,ÖZALP KIZILAY DENİZ,EMEKSİZ HAMDİ CİHAN,ABALI SAYGIN,Eklioğlu Beray Selver,KABA SULTAN,ANIK AHMET,BAŞ SERPİL,ÜNÜVAR TOLGA,BOLU SEMİH,ÖZGEN İLKER TOLGA,DOĞAN DURMUŞ,Çakır Esra Deniz,ŞEN YAŞAR,ANDIRAN NESİBE,ÇİZMECİOĞLU FİLİZ MİNE,EVLİYAOĞLU SAADET OLCAY,KARAGÜZEL GÜLAY,PİRGON MUSTAFA ÖZGÜR,ÇATLI GÖNÜL,Can Hatice Dilek,Gürbüz Fatih,Binay Çiğdem,Baş Veysel Nijat,Sağlam Celal,Gül Davut,Polat Adem,Cengizhan Açıkel,CİNAZ PEYAMİ. Growth curves for Turkish Girls with Turner Syndrome Results of the Turkish Turner Syndrome Study Group. Journal of Clinical Research in Pediatric Endocrinology. Cilt 7. sf 183-191, 2015. (Yayına Ulaşmak İçin Tıklayınız)
96. TEKİN BURAK,Atay Zeynep,ERGUN SAFİYE ATLAS TÜLİN,Can M,TÜNEY DAVUT,Babay S,TURAN SERAP,BEREKET ABDULLAH. H Syndrome A Multifaceted Histiocytic Disorder with Hyperpigmentation and Hypertrichosis. Acta Dermato Venereologica. Cilt 95. sf 1021-1023, 2015. (Yayına Ulaşmak İçin Tıklayınız)
DİĞER DERGİLERDE YAYIMLANAN MAKALELER
1. Anjum Omar,TURAN SERAP,BEREKET ABDULLAH. Reference data for bone speed of sound measurement by quantitative ultrasound in healthy children. Archives of Osteoporosis. Cilt 1. sf 37-41, 2007. (Yayına Ulaşmak İçin Tıklayınız)
2. Eser Çapan,TURAN SERAP,KILIÇOĞLU HÜLYA. CLINICAL AND CEPHALOMETRIC ANALYSIS OF THREE CASES WITH PYCNODYSOSTOSIS CASE REPORTS. Journal of Istanbul University Faculty of Dentistry. Cilt 49. sf 51-, 2015. (Yayına Ulaşmak İçin Tıklayınız)
3. DEMİRCİOĞLU SERAP,Bastepe Murat. Maternal Uniparental Disomy for Chromosome 20: Physical and Endocrinological Characteristics of Five Patients. The Journal of Clinical Endocrinology Metabolism. Cilt 103. sf 2083-2088, 2018. (Yayına Ulaşmak İçin Tıklayınız)
KİTAPLAR
ULUSLARARASI
BİLİMSEL KİTAP
KİTAP BÖLÜMÜ
1. DEMİRCİOĞLU SERAP,Bastepe Murat, Encyclopedia of Signaling Molecules, Cham. 2018.
2. TURAN SERAP,Bastepe Murat, Encyclopedia of Signaling Molecules, NewYork. 2017. (Yayına Ulaşmak İçin Tıklayınız)
ULUSAL
BİLİMSEL KİTAP
KİTAP BÖLÜMÜ
3. Özşen Ahu,TURAN SERAP, Yurdakök Pediatri, 2017.
4. BAŞ SERPİL,TURAN SERAP, Adolesan Sağlığı Koruyucu Hekimlik ve Erken Tanı, 2015.
5. BAŞ SERPİL,TURAN SERAP, Adolesan Sağlığı Koruyucu Hekimlik ve Erken Tanı, 2015.
6. TURAN SERAP,BAŞ SERPİL, Adolesan Sağlığı Koruyucu Hekimlik ve Erken Tanı, 2015.
7. TURAN SERAP,Çayır Atilla, Çocuk Endokrinolojisinde Uzlaşı II, 2015.
8. TURAN SERAP,BEREKET ABDULLAH, Neonatolojinin Temel İlkeleri ve Acilleri, 2007.
9. TURAN SERAP,BEREKET ABDULLAH, Neonatolojinin Temel İlkeleri ve Acilleri, 2007.
10. TURAN SERAP, Yenidoğan Dönemi Endokrin Hastalıkları, 2011.
11. Haliloğlu Belma,TURAN SERAP, Çocuklarda acil endokrin hastalıklar, 2013.
12. TURAN SERAP,BEREKET ABDULLAH, Çocuk Yoğun BakımEsaslar ve Uygulamalar, 2008.
13. BEREKET ABDULLAH,TURAN SERAP, Çocuk ve Adölasanda Endokrin Testler, 2006.
EDİTÖRLÜKLER
ULUSLARARASI
DERGİ
1. DEMİRCİOĞLU SERAP,BEREKET ABDULLAH,DARENDELİLER FATMA FEYZA,GÖKŞEN ŞİMŞEK RUHSAR DAMLA,ÖZEN SAMİM,DEMİR KORCAN Journal of Clinical Research in Pediatric Endocrinology
2. GÖKŞEN ŞİMŞEK RUHSAR DAMLA,TURAN SERAP,BEREKET ABDULLAH,DEMİR KORCAN,ÖZEN SAMİM,DARENDELİLER FATMA FEYZA Journal of Clinical Resarch in Pediatric Endocrinology
3. DARENDELİLER FATMA FEYZA,BEREKET ABDULLAH,GÖKŞEN ŞİMŞEK RUHSAR DAMLA,TURAN SERAP,DEMİR KORCAN,ÖZEN SAMİM Journal of Clinical Research in Pediatric Endocrinology (Yayına Ulaşmak İçin Tıklayınız)
BİLDİRİLER
ULUSLARARASI
1. DEMİRCİOĞLU SERAP, "Metabolic bone diseases in children, diagnosis related to oral and dental manifestations", International Association of Pediatric Dentistry Regional Meeting, 2018. (Yayına Ulaşmak İçin Tıklayınız)
2. KIRKGÖZ TARIK,ÖZHAN BAYRAM,ÇETİN GÖKHAN OZAN,KAYGUSUZ SARE BETÜL,DEMİRCİOĞLU SERAP,BEREKET ABDULLAH,GÜRAN TÜLAY, "Isolated Congenital Central Hypothyroidism due to a Novel Mutation in TSH Beta Subunit Gene", HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology, 2018.
3. BEREKET ABDULLAH,BUGRUL FUAT,KIRKGÖZ TARIK,KARADENİZ CERİT KIVILCIM,CANMEMİS ARZU,DEMİRCİOĞLU SERAP,PICARD JEAN YVES,TUĞTEPE HALİL,GÜRAN TÜLAY, "Persistent Mullerian duct syndrome: Rare But Important Aetiology of an Inguinal Hernia and Cryptorchidism in Boys", HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology, 2018.
4. KAYGUSUZ SARE BETÜL,YEŞİL GÖZDE,KIRKGÖZ TARIK,DEMİRCİOĞLU SERAP,BEREKET ABDULLAH, "An 18 Month Old Boy with Hypoglycemic Convulsion and Obesity Due to POMC Deficiency", HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology, 2018.
5. 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)
6. [Mantovani Giovanna,Bastepe Murat,Monk David,De Sanctis Luisa,Thiele Susanne,Usardi Alessia,Ahmed Faisal,Bufo Roberto,Choplin Timothee,DeFillipo Gianpaolo,Devernois Guillemette,Eggermann Thomas,Elli Francesca,Freson Kathleen,Garcia Ramirez Aurora,Germain-Lee Emily,Groussin Lionel,Hamdy Neveen,Hanna Patrick,Hiort Olaf,Juppner Harald,Kamenicky Peter,Knight Nina,Kottler MarieLaure,Le Norcy Elvire,Lecumberri Beatriz,Levine Michael A,Makiti Outi,Martin Regina,Angel MartosMoreno Gabriel,Minagawa Masanori,Muray Philip,Pereda Arrate,Pignolo Roberto,Rejnmark Lars,Rodado Rebecca,Rothenbuhler Anya,Saraff Vrinda,Shoemaker Ashley,Shore Eileen M,Silve Caroline,Turan Serap,DEMİRCİOĞLU SERAP,Woods Philip,Zillikens M Carola,Perez de Nanclares Guimar,Linglart Agnes, "Diagnosis and Management of Pseudohypoparathyroidism and Related Disorders: First International Consensus Statement", HORMONE RESEARCH IN PAEDIATRICS, 2018. (Yayına Ulaşmak İçin Tıklayınız)
7. 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.
8. 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)
9. 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.
10. Yıldız Melek,TURAN SERAP,Akçay Teoman,Atay Zeynep,ÖNAL HASAN,Barış Tugba,HAKLAR GONCAGÜL,BEREKET ABDULLAH,Guran Tulay, "17OH-pregnenolone seems a major drive of androgen excess in patient with 11 beta hydroxylase deficiency", 10th Joint Meeting of Paediatric Endocrinology, Washington, 2017.
11. 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.
12. 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.
13. HATUN ŞÜKRÜ,YEŞİLTEPE MUTLU GÜL,CİNAS PEYAMİ,YILDIZ ERBAŞ MELEK,AKÇAY TEOMAN,ÖNAL HASAN,TURAN SERAP,EKBERZADE AZAD,BEREKET ABDULLAH,BOLU SEMİH,ARSLANOĞLU İLKNUR,DÖĞER ESRA,ARASLI YILMAZ ASLIHAN,UÇAKTÜRK AHMET,SEYMEN kARABULUT GÜLCAN,ÜNVER TUHAN HALE,DEMİR KORCAN,SAVAŞ ERDEVE ŞENAY,AYCAN ZEHRA,GÜNGÖR NESLİHAN, "CLINICAL CHARACTERISTICS OF TURKISH CHILDREN AND ADOLESCENTS WITH TYPE 2 DIABETES", 10th International Meeting of Pediatric Endocrinology, 2017.
14. 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.
15. 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.
16. HATUN ŞÜKRÜ,Yeşiltepe Mutlu Gül,CİNAZ PEYAMİ,Yıldız Erbaş melek,Akçay Teoman,ÖNAL HASAN,TURAN SERAP,ekberzade azad,BEREKET ABDULLAH,bolu semih,döger esra,araslı yılmaz aslıhan,uçaktürk ahmet,seymen karabulut gülcan,ÜNVER TUHAN HALE,DEMİR KORCAN,SAVAŞ ERDEVE ŞENAY,AYCAN ZEHRA,Güngör Neslihan, "Clinical characteristics of Turkish children and adolescents with type 2 diabetes", 10th International Meeting of Pediatric Endocrinology, 2017.
17. TURAN SERAP, "Current Perspective on Pseudohypoparathyroidism New Classification", Current Trends in Pediatric Endocrinology-A PES Perspective, 2016.
18. BAŞ SERPİL,GÜRAN TÜLAY,ATAY ZEYNEP,Haliloğlu Belma,ABALI SAYGIN,TURAN SERAP,BEREKET ABDULLAH, "Premature Puberche Hyperinsülinemia Hypothyroxenemia and Hyperintensities in Basal Ganglia All Caused by a Single Congenital Defect", Current Trends in Pediatric Endocrinology- A, 2016.
19. Thiele Susanne,Mantovani Giovanna,Barlier Anne,Bordogna Paola,Elli Francesca,Freson Kathleen,Garin Intza,Grybek Virginie,Hanna Patrick,Izzi Benedetta,Hiort Olaf,Lecumberri Beatriz,Pereda Arrate,de Sanctis Luisa,Silve Caroline,TURAN SERAP,Usardi Alessia,Saraff Vrinda,de Nanclares Guiomar Perez,Linglart Agnes, "From Pseudohypoparathyroidism to Inactivating PTH PTHrP Signaling Disorder iPPSD a Novel Classification Proposed by the European EuroPHP Network", 55th Annual Meeting of the ESPE, 2016.
20. ABALI SAYGIN,ARMAN AHMET,ATAY ZEYNEP,BAŞ SERPİL,ÇAM SEVDA,Görmez Zeliha,Demirci Hüseyin,ALANAY YASEMİN,AKARSU AYŞE NURTEN,BEREKET ABDULLAH,TURAN SERAP, "Nonsense Mutation in SPARC Gene Causing Autosomal Recessive Ostegenesis Imperfecta", 55th Annual Metting of the ESPE Paris, 2016.
21. Fernandez Isabelle,Ahmed Syed Faisal,Bishop Nick,Brandi Maria Luisa,Doulgeraki Artemis,Haeusler Gabriele,Hogler Wolfgang,Kostik Mikhail,Makitie Outi,Moreno Gabriel Martos,Nilsson Ola,Schnabel Dirk,Sumnik Zdenek,Tillmann Vallo,TURAN SERAP,Zillikens Carola,Linglart Agnes, "A European Survey to Identify New Roads for Care Training and Research Around Rare Metabolic Bone Diseases", 55th Annual Meeting of the ESPE, Paris, 2016.
22. ABALI SAYGIN,ARMAN AHMET,ATAY ZEYNEP,BEREKET ABDULLAH,BAŞ SERPİL,Haliloğlu Belma,GÜRAN TÜLAY,Görmez Zeliha,Demirci Hüseyin,AKARSU AYŞE NURTEN,TURAN SERAP, "Frequency of Recessive Osteogenesis Imperfecta in a Turkish Cohort and Genetic Causes", 55th Annual Meeting of the ESPE, Paris, 2016.
23. Ozcan Sibel,ABALI SAYGIN,ATAY ZEYNEP,Haliloğlu Belma,BAŞ SERPİL,Öztürk Gamze,ÇAM SEVDA,Akçay Teoman,GÜRAN TÜLAY,BEREKET ABDULLAH,TURAN SERAP, "Etiologic Distribution and Characteristics of Patients with Short Stature in a Pediatric Endocrinology Clinic", 55th Annual Meeting of the ESPE, 2016.
24. BEREKET ABDULLAH,Bugur Ibrahin Sinan,GÜRAN TÜLAY,ATAY ZEYNEP,Ekberzade Azad,Gurbanov Ziya,ÖGE ECE,Tas Cektar Seyid Riza,TURAN SERAP,FURMAN ANDRZEJ, "Reconsideration of Mid Parental Height Calculation", 55th Annual Meeting of the ESPE, 2016.
25. Ekberzade Azad,ABALI SAYGIN,BAŞ SERPİL,ATAY ZEYNEP,Gurbanov Ziya,TURAN SERAP,GÜRAN TÜLAY,BEREKET ABDULLAH, "beta hCG from an Occult Source Causing Peripheral Precocious Puberty Identification of the Tumour 6 Years After Presentation", 55th Annual Meeting of the ESPE, 2016.
26. BAŞ SERPİL,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", 55th Annual Meeting of the ESPE, 2016.
27. Muzafferova Nigar,BAŞ SERPİL,ATAY ZEYNEP,BEREKET ABDULLAH,TURAN SERAP, "The Effect of Subclinical Hypothyroidism SH and Treatment of SH with L T4 on Basal Metabolic Rate in Obese Children A Prospective Study", 55th Annual Meeting of the ESPE, Paris, 2016.
28. TURAN SERAP,ABALI SAYGIN, "Neonatal Hypocalcemia", 55th Annual Meeting of the ESPE, Paris, 2016.
29. TURAN SERAP, "Growth Hormone Deficiency and Treatment", 59th Turkish National Pediatric Congress joint with the 3rd Italian-Turkish-Iranian Pediatric Congress, 2015.
30. GÜRAN TÜLAY,Buonocore Federica,SAKA NURÇİN,ÖZBEK MEHMET NURİ,AYCAN ZEHRA,BEREKET ABDULLAH,BAŞ FİRDEVS,DARCAN ŞÜKRAN,BİDECİ AYSUN,TURAN SERAP,GÜVEN AYLA,TARIM ÖMER FARUK,YILMAZ AĞLADIOĞLU SEBAHAT,ATAY ZEYNEP,ÖZEN SAMİM,DEMİR KORCAN,AKINCI AYŞEHAN,KÜÇÜKEMRE AYDIN BANU,BÜYÜKİNAN MUAMMER,YÜKSEL BİLGİN,YILDIZ METİN,AKÇAY TEOMAN,KARA CENGİZ,ÖZGEN İLKER TOLGA,ÇATLI GÖNÜL,IŞIK EMREGÜL,BOLU SEMİH,ÖZHAN BAYRAM,GÜRBÜZ FATİH,UÇAR AHMET,DEMİRBİLEK HÜSEYİN,YAVAŞ ABALI ZEHRA,ESRA DÖGER,EREN ERDAL,BERBEROĞLU MERİH,HACIHAMDİOĞLU BÜLENT,ACHERMANN JOHN, "Primary Adrenal Insufficiency in Children without Congenital Adrenal Hyperplasia Molecular and Clinical Characterisation of a Nationwide Cohort", 54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 2015.
31. Atay Zeynep,Yeşilkaya Ediz,Erdeve Şenay,AKIN LEYLA,EREN ERDAL,Döger Esra,AYCAN ZEHRA,Abali Zehra,AKINCI AYŞEHAN,ŞIKLAR ZEYNEP,ÖZEN SAMİM,KARA CENGİZ,TAYFUN MELTEM,TÜTÜNCÜLER FİLİZ,SEYMEN KARABULUT GÜLCAN,KARAGÜZEL GÜLAY,SAĞLAM HALİL,BİDECİ AYSUN,KURTOĞLU SELİM,BEREKET ABDULLAH,TURAN SERAP,SARI ERKAN,ÇETİNKAYA SEMRA,GÜRAN TÜLAY, "Aetiological Spectrum and Clinical Characteristics of 129 Children with Gonadotropin Independent Precocious Puberty A Nationwide Cohort Study", 54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 2015.
32. ABALI SAYGIN,TAMURA MAYUKO,ATAY ZEYNEP,İŞGÜVEN ŞÜKRİYE PINAR,GÜRAN TÜLAY,HALİLOĞLU TÜLAY,BAŞ SERPİL,ISOJIMA TSUYOSHI,TURAN SERAP,KITANAKA SACHIKA,BEREKET ABDULLAH, "Hereditary Vitamin D Resistant Rickets Report of Four Cases with Successful Use of Intermittent Intravenous Calcium Via Peripheral Route", 54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 2015.
33. BAŞ SERPİL,ABALI SAYGIN,ATAY ZEYNEP,GURBANOV ZİYA,TURAN SERAP,BEREKET ABDULLAH, "Friedreich s Ataxia Presenting with Diabetes Mellitusin an Adolescent", 54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 2015.
34. TURAN SERAP,GURBANOV ZİYA,BAŞ SERPİL,ABALI SAYGIN,ATAY ZEYNEP,BEREKET ABDULLAH, "Central or Primary Hypothyroidism How toDifferentiate in Patients with Low T4 but MildlyElevated TSH Levels", 54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 2015.
35. ABALI SAYGIN,BAŞ SERPİL,AKBARZADE AZAD,ATAY ZEYNEP,HALİLOĞLU BELMA,GÜRAN TÜLAY,TURAN SERAP,BEREKET ABDULLAH, "Evaluating First Year Response and Final Height toGrowth Hormone Treatment in Growth HormoneDeficiency Based on Peak GH Levels on Testing", 54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 2015.
36. BAŞ SERPİL,ABALI SAYGIN,ATAY ZEYNEP,HALİLOĞLU BELMA,GURBANOV ZİYA,GÜRAN TÜLAY,BEREKET ABDULLAH,TURAN SERAP, "Factors Effecting Response to Growth HormoneTreatment in Children with Turner Syndrome", 54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 2015.
37. BİDECİ AYSUN,YEŞİLKAYA EDİZ,BERBEROĞLU MERİH,ŞIKLAR ZEYNEP,DARCAN ŞÜKRAN,ÖZEN SAMİM,BAŞ SERPİL,DÖGER ESRA,EREN ERDAL,TURAN SERAP,AKINCI AYŞEHAN,DEMİREL FATMA,ŞİMŞEK ENVER,ÇETİNKAYA SEMRA,BİRCAN İFFET,AYDIN HASAN MURAT,BÖBER ECE,SARI ERKAN,HATİPOĞLU NİHAL,TAYFUN MELTEM,SAĞLAM HALİL,ÖZBEK MEHMET NURİ,YILDIRIM RUKEN,DÜNDAR BUMİN NURİ,ÇAYIR ATİLLA,ALAGÖZ ENGİN,ATAŞ ERMAN, "The Diagnostic Treatment and Follow Up Features of Childhood Thyroid Malignancies A Preliminary Report", 54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 2015.
38. TURAN SERAP,Mumm Steven,Gottesman Gary S,ABALI SAYGIN,BAŞ SERPİL,atay zeynep,H McAlister William,Whyte Michael P, "Dysosteosclerosis from a unique mutation in SLC29A3", 7th International Conference on Children's Bone Health, 2015.
39. POYRAZOĞLU ŞÜKRAN,AKÇAY TEOMAN,ATABEK MEHMET EMRE,BİDECİ AYSUN,BİRCAN İFFET,BÖBER ECE,CAN ŞULE,DARCAN ŞÜKRAN,ERSOY BETÜL,GÜVEN AYLA,KARA CENGİZ,KESKİN MEHMET,KURTOĞLU SELİM,ÖZBEK MEHMET NURİ,ÖZGEN İLKER TOLGA,ŞIKLAR ZEYNEP,ŞİMŞEK ENVER,TURAN SERAP,YÜKSEL BİLGİN,DARENDELİLER FATMA FEYZA, "Current Practice in Diagnosis and Treatment of GH Deficiency in Childhood A Survey from Turkey", 54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 2015.
ULUSAL
40. DEMİRCİOĞLU SERAP, "KEMİK MİNERAL DENSİTE YÜKSEKLİĞİ İLE KARAKTERİZE İSKELETİN GENETİK HASTALIKLARI", İSKELETİN GENETİK HASTALIKLARI KURSU, 2018.
41. TURAN SERAP,Gurbanov Ziya,BAŞ SERPİL,ABALI SAYGIN,ATAY ZEYNEP, "Serbest T4 Düşük TSH Hafif Yüksek Olgularda Santral Hipotiroidi Primer Hipotiroidi Ayrımını Nasıl Yapabiliriz", 19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, 2015.
42. TURAN SERAP, "GEÇ ÇOCUKLUK ERKEN ERGENLİK", KANUNİ SULTAN SÜLEYMAN GÜNLERİ, 2015.
43. TURAN SERAP, "YILLIK", 19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, 2015.
44. TURAN SERAP, "Temel genetik kavramlar ve kalıtım şekilleri", 1. Pediatrik Endokrinolojiye Giriş Kursu, 2015.
45. BAŞ SERPİL,ABALI SAYGIN,ATAY ZEYNEP,GURBANOV ZİYA,HALİLOGLU BELMA,GÜRAN TÜLAY,TURAN SERAP,BEREKET ABDULLAH, "Merkezi Yenidogan Tarama Programi ile Tani Almis Konjenital Hipotiroidili Vakalarimizin İzlemi", 19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, 2015.
46. ÖZCAN SİBEL,ABALI SAYGIN,ATAY ZEYNEP,HALİLOĞLU BELMA,BAŞ SERPİL,ÖZTÜRK GAMZE,AKÇAY TEOMAN,GÜRAN TÜLAY,TURAN SERAP,BEREKET ABDULLAH, "Boy Kısalığı Olan Hastalarda Özellikler ve Etiyolojik Dağılım Bir Çocuk Endokrinoloji Kliniği Verileri", 19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, 2015.
47. ATAY ZEYNEP,YEŞİLKAYA EDİZ,SAVAŞ ŞENAY,TURAN SERAP,AKIN LEYLA,EREN ERDAL,DÖĞER ESRA,AYCAN ZEHRA,YAVAŞ ABALI ZEHRA,AKINCI AYŞEHAN,ŞIKLAR ZEYNEP,ÖZEN SAMİM,KARA CENGİZ,TAYFUN MELTEM,SARI ERKAN,TÜTÜNCÜLER FİLİZ,SEYMEN KARABULUT GÜLCAN,KARAGÜZEL GÜLAY,ÇETİNKAYA SEMRA,SAĞLAM HALİL,BİDECİ AYSUN,KURTOĞLU SELİM,GÜRAN TÜLAY,BEREKET ABDULLAH, "Periferal Puberte Prekokslu 129 Çocukta Etiyolojik Dağılım Ve Klinik Özellikler", 19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, 2015.
48. ABALI SAYGIN,ARMAN AHMET,ATAY ZEYNEP,BAŞ SERPİL,GÜRAN TÜLAY,GÖRMEZ ZELİHA,DEMİRCİ HÜSEYİN,BEREKET ABDULLAH,TURAN SERAP, "Otozomal Resesif Osteogenezis İmperfekta Populasyonumuzdaki Sıklığı Ve Genetik Nedenleri", 19. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, 2015.
49. ABALI SAYGIN,AKCAN NEŞE,TOKSOY GÜVEN,ATAY ZEYNEP,UYGUNER ZEHRA OYA,BAŞ FİRDEVS,GÜRAN TÜLAY,BAŞ SERPİL,KIRMIZIPEKMEZ HEVES,POYRAZOĞLU ŞÜKRAN,KAYSERİLİ KARABEY HÜLYA,TURAN SERAP,DARENDELİLER FATMA FEYZA,BEREKET ABDULLAH,BUNDAK RÜVEYDE, "Nonklasik Konjenital Adrenal Hiperplazi Hastalarının Genotip Ve Fenotip Özellikleri", 19. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, 2015.
50. ŞIKLAR ZEYNEP,BERBEROĞLU MERİH,GENENS MİKAYİR,POYRAZOĞLU ŞÜKRAN,BAŞ FİRDEVS,DARENDELİLER FATMA FEYZA,BUNDAK RÜVEYDE,AYCAN ZEHRA,ERDEVE SAVAŞ,ÇETİNKAYA SEMRA,GÜVEN AYLA,ABALI SAYGIN,ATAY ZEYNEP,TURAN SERAP,KARA CENGİZ, "Ulusal Düzeyde Noonan Sendromlu Olgularin Klinik Özellikleri ve Büyüme İzlemlerinin Değerlendirilmesi", 19. ÇOCUK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, 2015.
YAYINLANMAMIŞ BİLDİRİLER
ULUSLARARASI
1. TURAN SERAP, "CAH Congenital Adrenal Hyperplasia", ESPE Winter School
2. DEMİRCİOĞLU SERAP, "CONGENITAL ADRENAL HYPERPLASIA", EUROPEAN SOCİETY FOR PEDIATRIC ENDOCRINOLOGY WINTER SCHOOL
3. TURAN SERAP, "Congenital Adreal Hyperplasia", European Society for Paediatric Endocrinology-Winter School
4. DEMİRCİOĞLU SERAP, "DISORDER OF ADRENAL EXCESS AND ADRENAL MEDULLA", EUROPEAN SOCİETY FOR PEDIATRIC ENDOCRINOLOGY WINTER SCHOOL
5. DEMİRCİOĞLU SERAP, "DISORDER OF SEXUEL DEVELOPMENT", EUROPEAN SOCİETY FOR PEDIATRIC ENDOCRINOLOGY WINTER SCHOOL
6. TURAN SERAP, "Disoerder of Adrenocortical Excess and Adrenal Medulla", ESPE Winter School
7. TURAN SERAP, "Disorders of adrenocortical excess and adrenal medulla", European Society for Paediatric Endocrinology Winter School
8. TURAN SERAP, "Disorders of sexual differentiation", European Society for Paediatric Endocrinology Winter School
9. TURAN SERAP, "Disorders of SExual Differentiation", ESPE Winter School
10. DEMİRCİOĞLU SERAP, "ESPE Bone and Growth Plate Working Group (BGP)- Case Presentation", 57th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE)
11. DEMİRCİOĞLU SERAP, "INTRODUCTION TO MOLECULAR ENDOCRINOLOGY", EUROPEAN SOCİETY FOR PEDIATRIC ENDOCRINOLOGY WINTER SCHOOL
12. TURAN SERAP, "Introduction to molecular endocrinology", European Society for Paediatric Endocrinology Winter School
13. TURAN SERAP, "Introduction to Molecular Endocrinology", ESPE Winter School
14. TURAN SERAP,TOPALOĞLU ALİ KEMAL, "Late Breaking news", Current Trends in Pediatric Endocrinology-A PES perspective
ULUSAL
15. DEMİRCİOĞLU SERAP, "BOY KISALIĞINA GENEL YAKLAŞIM", İSKELETİN GENETİK HASTALIKLARI KURSU
16. TURAN SERAP, "Diyabet ile yaşam", Diyabet ile Yaşam- Cerrahpaşa
17. DEMİRCİOĞLU SERAP, "Düşük Alkali Fosfotaz Düzeyinin Önemi", 40. Pediatri Günleri ve 19. Pediatri Hemşireliği Günleri
18. TURAN SERAP, "HİPOTİROİDİ VE TİROTOKSİKOZUN YENİDOĞAN ÜZERİNE ETKİSİ", GEBELİK VE TİROİD SEMPOZYUMU
19. TURAN SERAP, "HPP Genel Değerlendirme", HİPOFOSFATAZYA DANIŞMA KURULU TOPLANTISI
20. DEMİRCİOĞLU SERAP, "KEMİK MİNERAL DANSİTE DÜŞÜKLÜĞÜ İLE KARAKTERİZE İSKELETİN GENETİK HASTALIKLATI", İSKELETİN GENETİK HASTALIKLARI KURSU
21. DEMİRCİOĞLU SERAP, "Psödohipoparatiroidi tanı ve tedavisi", Pediatrik Endokrinoloji İleri Kursu
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