Faculty of Medicine

Academic Members

Cengiz  Kara

Cengiz Kara,  Prof.

Öğretim Üyesi

Professor Dr. Cengiz Kara graduated from Ankara High School in 1985 and Ankara University Faculty of Medicine in 1991. He completed his residency in Pediatrics in 1996 and his fellowship program in Pediatric Endocrinology and Metabolism in 2005 at Dr. Sami Ulus Children’s Hospital (Ankara). Since joining Ondokuz Mayıs University of Samsun in 2007 as an Assistant Professor of Pediatrics, along with his regular faculty responsibilities, Dr. Kara also completed a PhD program in Molecular Medicine at the Institute of Graduate Studies. Dr. Kara received his Associate Professor and Professor degrees in 2010 and 2016, respectively. He is currently the faculty member of the Department of Pediatrics, Faculty of Medicine, Istinye University. He is the author of numerous national /international scientific articles and awards with h-index of 13. His primary research interest is focused on the clinic and genetics of congenital hypothyroidism. Dr. Kara is a member of European Society for Pediatric Endocrinology (ESPE). Since 2017, he has been the deputy vice-president of the Turkish Society for Pediatric Endocrinology and Diabetes (TSPED). Dr. Kara has organized and chaired a number of basic and advanced educational meetings for fellows and specialists of pediatric endocrinology, that have shaped clinical practice in Turkey. He speaks English and is married with two children.

Research Areas: Pediatric Endocrinology, Congenital Hypothyroidism

Main Areas: Çocuk Endokrinolojisi, 

2020 - Revisiting Classical 3β-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric Cases
GÜRAN TÜLAY, KARA CENGİZ, YILDIZ MELEK, ÇELEBİ BİTKİN EDA, HAKLAR GONCAGÜL, Lin Jen-Chiech, KESKİN MEHMET, BERNARD LISE, ANIK AHMET, ÇATLI GÖNÜL, GÜVEN AYLA, KIREL BİRGÜL, TÜTÜNCÜLER KÖKENLİ FİLİZ, ÖNAL HASAN, DEMİRCİOĞLU SERAP, Akçay Teoman, ATAY ZEYNEP, CAN YILMAZ GÜLAY, MAMMADOVA JAMALA, AKBARZADE AZAD, ŞİRİKÇİ ÖNDER, BARIŞ TUĞBA, CHUNG BON CHU, BEREKET ABDULLAH. The Journal of Clinical Endocrinology & Metabolism, 105(4), 1718-1728.
2020 - Utility of estimated glucose disposal rate for predicting metabolic syndrome in children and adolescents with type-1 diabetes
YAYICI KÖKEN ÖZLEM, KARA CENGİZ, CAN YILMAZ GÜLAY, AYDIN HASAN MURAT. Journal of Pediatric Endocrinology and Metabolism, 33(7), 859-864.
2020 - Prevalence of Obesity and Metabolic Syndrome in Children with Type 1 Diabetes: A Comparative Assessment Based on Criteria Established by the International Diabetes Federation, World Health Organisation and National Cholesterol Education Program
YAYICI KÖKEN ÖZLEM, KARA CENGİZ, CAN YILMAZ GÜLAY, AYDIN HASAN MURAT. Journal of Clinical Research in Pediatric Endocrinology, 12(1), 55-62.
2020 - Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 Infants
GÜRAN TÜLAY, TEZEL BAŞAK, ÇAKIR MELTEM, AKINCI AYŞEHAN, ORBAK ZERRİN, KESKİN MEHMET, SELVER EKLİOĞLU BERAY, ÖZÖN ZEYNEP ALEV, Özbek Mehmet Nuri, KARAGÜZEL GÜLAY, HATİPOĞLU NİHAL, ÇİZMECİOĞLU FİLİZ MİNE, KARA CENGİZ, ŞİMŞEK ENVER, BAŞ FİRDEVS, AYDIN HASAN MURAT, DARENDELİLER FATMA FEYZA. Journal of Clinical Research in Pediatric Endocrinology, 12(3),
2019 - Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants
GÜRAN TÜLAY,TEZEL BAŞAK,GÜRBÜZ FATİH,Eklioğlu Beray Selver,HATİPOĞLU NİHAL,KARA CENGİZ,AYDIN HASAN MURAT,ŞİMŞEK ENVER,ÇİZMECİOĞLU FİLİZ MİNE,ÖZÖN ZEYNEP ALEV,BAŞ FİRDEVS,DARENDELİLER FATMA FEYZA. Journal of Clinical Research in Pediatric Endocrinology, 13-23.
2019 - 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
ABACI AYHAN,ÇATLI GÖNÜL,ÖZGÜR KIRBIYIK,MURATOĞLU ŞAHİN NURSEL,YAVAŞ ABALI ZEHRA,ÜNAL EDİP,ŞIKLAR ZEYNEP,MENGEN EDA,ÖZEN SAMİM,GÜRAN TÜLAY,KARA CENGİZ,YILDIZ METİN,EREN ERDAL,NALBANTOĞLU ÖZLEM,GÜVEN AYLA,ÇAYIR ATİLLA,DEMİR AKBAŞ EMİNE,KOR YILMAZ,ÇÜREK YUSUF,BAŞ FİRDEVS,DARCAN ŞÜKRAN,BERBEROĞLU MERİH. Journal of Endocrinological Investigation, 42(4), 453-470.
2018 - Acoustic Radiation Force Impulse Quantification in the Evaluation of Thyroid Elasticity in Pediatric Patients With Hashimoto Thyroiditis
YÜCEL SERAP,CEYHAN BİLGİCİ MELTEM NECİBE,KARA CENGİZ,Can Yilmaz Gulay,AYDIN HASAN MURAT,ELMALI MUZAFFER,TOMAK LEMAN,SAĞLAM DİLEK. Journal of ultrasound in medicine, 37(5), 1143-1149.
2018 - Comparison of Treatment Regimens for the Management of Severe Hypercalcemia due to Vitamin D Intoxication in Children
DEMİR KORCAN,DÖNERAY HAKAN,KARA CENGİZ,ATAY ZEYNEP,Çayır Atilla,ANIK AHMET,EREN ERDAL,UÇAKTÜRK AHMET,CAN YILMAZ GÜLAY,Törel Ergür Ayça,KENDİRCİ MUSTAFA,AYCAN ZEHRA,BEREKET ABDULLAH,AYDIN HASAN MURAT,ORBAK ZERRİN,ÖZKAN BEHZAT. Journal of Clinical Research in Pediatric Endocrinology, 9(), 182-184.
2018 - Nationwide hypophosphatemic rickets study57th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE)
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. Hormone Research in Paediatrics, 90(1), 109-110.
2018 - Gebelikte tiroid hastalıklarının neonatal etkileri ve TSH yüksekliği olan bebeğe yaklaşım: Türk Neonatoloji ve Çocuk Endokrinoloji ve Diabet Dernekleri Uzlaşı Raporu
ÖZÖN ZEYNEP ALEV,TEKİN AYŞE NESLİHAN,ŞIKLAR ZEYNEP,KARA CENGİZ,GÜLCAN HANDE,TAŞTEKİN AYHAN,DEMİR KORCAN,KOÇ ESİN,EVLİYAOĞLU SAADET OLCAY,Kurtoğlu Selim. Türk Pediatri Arşivi, 53(), 209-223.
2018 - Analysis of the GCK gene in 79 MODY type 2 patients: A multicenter Turkish study, mutation profile and description of twenty novel mutations
AYKUT AYÇA,KARACA EMİN,ONAY HÜSEYİN,Goksen Damla,ÇETİNKALP ŞEVKİ,EREN ERDAL,ERSOY BETÜL,Çakır Esra Papatya,BÜYÜKİNAN MUAMMER,KARA CENGİZ,ANIK AHMET,Kırel Birgül,ÖZEN SAMİM,ATİK TAHİR,DARCAN ŞÜKRAN,ÖZKINAY FERİŞTAH FERDA. Gene, 641(), 186-189.
2018 - Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants.
GÜRAN TULAY,TEZEL BAŞAK,GÜRBÜZ FATİH,SELVER EKLİOĞLU BERAY,HATİPOĞLU NİHAL,KARA CENGİZ,ŞİMŞEK ENVER,ÇİZMECİOĞLU FİLİZ MİNE,OZON ALEV,BAŞ FİRDEVS,AYDIN HASAN MURAT,DARENDELİLER FATMA FEYZA. Journal of Clinical Research in Pediatric Endocrinology,
2017 - Transient Neonatal Diabetes with Fanconi Bickel Syndrome
OZSU ELİF,KARA CENGİZ,YILMAZ GÜLAY CAN,TEPE DERYA,AYDIN HASAN MURAT. Medicine Science | International Medical Journal, 6(1), 111-113.
2017 - Does Type 1 Diabetes Mellitus Affect the Shear Wave Velocity of the Thyroid Gland of Children Without Autoimmune Thyroiditis?
SAĞLAM DİLEK,CEYHAN BİLGİCİ MELTEM NECİBE,KARA CENGİZ,Can Yılmaz Gülay,TANRIVERMİŞ SAYIT ASLI. Ultrasound Quarterly, 33(3), 225-228.
2017 - Acoustic Radiation Force Impulse Imaging in the Differential Diagnosis of an Ectopic Intrathyroidal Thymus
SAĞLAM DİLEK,CEYHAN BİLGİCİ MELTEM NECİBE,KARA CENGİZ,ELMALI MUZAFFER,TANRIVERMİŞ SAYIT ASLI. International Journal of Radiology and Radiation Oncology, 3(1), 10-12.
2017 - Role of Point Shear Wave Elastography in the Determination of the Severity of Fibrosis in Pediatric Liver Diseases With Pathologic Correlations
Özkan Mehmet Burak,CEYHAN BİLGİCİ MELTEM NECİBE,EREN ESRA,ÇALTEPE GÖNÜL,Yilmaz Gulay,KARA CENGİZ,Gün Seda. Journal of Ultrasound in Medicine, 36(11), 2337-2344.
2016 - Pubertenin Epigenetik Kontrolü
KARA CENGİZ,OĞUR METHİYE GÖNÜL. Türkiye Klinikleri Pediatrik Bilimleri, 12(4), 136-45.
2016 - Multisystemic Severe Form Pseudohypoaldosteronism Can Gastrostomy be Useful in the Management
ÖNDER AŞAN,ÇETİNKAYA SEMRA,KARA CENGİZ,ZENCİROĞLU AYŞEGÜL,AYCAN ZEHRA. Turkish Journal of Pediatric Disease, 10(2), 134-136.
2016 - The Growth Characteristics of Patients with Noonan Syndrome Results of Three Years of Growth Hormone Treatment A Nationwide Multicenter Study
ŞIKLAR ZEYNEP,MİKAYİR GENENS,POYRAZOĞLU ŞÜKRAN,BAŞ FİRDEVS,DARENDELİLER FATMA FEYZA,BUNDAK RÜVEYDE,AYCAN ZEHRA,ERDEVE ŞENAY,ÇETİNKAYA SEMRA,GÜVEN AYLA,ABALI SAYGIN,ATAY ZEYNEP,TURAN SERAP,KARA CENGİZ,CAN YILMAZ GÜLAY,AKYÜREK NESİBE,ABACI AYHAN,ÇELMELİ GAMZE,SARI ERKAN,BOLU SEMİH,KORKMAZ HÜSEYİN AVNİ,ŞİMŞEK ENVER,ÇATLI GÖNÜL,BÜYÜKİNAN MUAMMER,ÇAYIR ATİLLA,EVLİYAOĞLU SAADET OLCAY,İŞGÜVEN ŞÜKRİYE PINAR,ÖZGEN İLKER TOLGA,ELHAN ATİLLA HALİL,BERBEROĞLU MERİH. Journal of Clinical Research in Pediatric Endocrinology, 8(3), 305-312.
2016 - The Etiology and Clinical Features of Non CAH Gonadotropin Independent Precocious Puberty A Multicenter Study
ATAY ZEYNEP,YEŞİLKAYA EDİZ,ERDEVE ŞENAY,TURAN SERAP,AKIN LEYLA,EREN ERDAL,DOGER 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. The Journal of Clinical Endocrinology & Metabolism, 101(5), 1980-1988.
2016 - Evaluation of therapeutics management patterns and glycemic control of pediatric type 1 diabetes mellitus patients in Turkey A nationwide cross sectional study
HATUN ŞÜKRÜ,DEMİRBİLEK HÜSEYİN,DARCAN ŞÜKRAN,YÜKSEL AYŞEGÜL,BİNAY ÇİĞDEM,GÖKŞEN ŞİMŞEK RUHSAR DAMLA,KARA CENGİZ,ÇETİNKAYA ERGUN,ÜNÜVAR TOLGA,UÇAKTÜRK AHMET,TÜTÜNCÜLER FİLİZ,CESUR YAŞAR,BUNDAK RÜVEYDE,SAĞLAM HALİL,ŞİMŞEK ENVER,BEREKET ABDULLAH. Diabetes Research and Clinical Practice, 119(), 32-40.
2016 - Transient Congenital Hypothyroidism in Turkey An Analysis on Frequency and Natural Course
KARA CENGİZ,GÜNİNDİ GÜLSÜM FİGEN,CAN YILMAZ GÜLAY,AYDIN HASAN MURAT. Journal of Clinical Research in Pediatric Endocrinology, 8(2), 170-179.
2016 - Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome
Sarı Erkan,BEREKET ABDULLAH,YEŞİLKAYA EDİZ,BAŞ FİRDEVS,BUNDAK RÜVEYDE,AYDIN BANU KÜÇÜKEMRE,DARCAN ŞÜKRAN,DÜNDAR BUMİN NURİ,BÜYÜKİNAN MUAMMER,KARA CENGİZ,ADAL SERVET ERDAL,AKINCI AYŞEHAN,ATABEK MEHMET EMRE,DEMİREL FATMA,ÇELİK NURULLAH,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,ÖKTEN AYŞENUR,ABACI AYHAN,DÖNERAY HAKAN,ÖZBEK MEHMET NURİ,KESKİN MEHMET,ÖNAL HASAN,AKYÜREK NESİBE,BULAN K,TEPE DERYA,EMEKSİZ HAMDİ CİHAN,DEMİR KORCAN,ÖZALP KIZILAY DENİZ,TOPALOĞLU ALİ KEMAL,EREN ERDAL,ÖZEN SAMİM,DEMİRBİLEK HÜSEYİN,ABALI SAYGIN,AKIN LEYLA,SELVER EKLİOĞLU BERAY,KABA SULTAN,ANIK AHMET,BAŞ SERPİL,ÜNÜVAR TOLGA,SAĞLAM HALİL,BOLU SEMİH,ÖZGEN İLKER TOLGA,CİNAZ PEYAMİ. American Journal of Medical Genetics Part A, 170(4), 942-948.
2016 - Efficacy and safety of pamidronate in children with vitamin D intoxication
KARA CENGİZ,ÇETİNKAYA SEMRA,GÜNDÜZ SUZAN,Can Yılmaz Gülay,AYCAN ZEHRA,AYDIN HASAN MURAT. Pediatrics International, 58(7), 562-568.
2015 - Association between autoimmune thyroid diseases and Neurofibromatosis type 1 is endocrinological evaluation necessary for children with Neurofibromatosis type 1
KARA CENGİZ. Journal of Clinical Research in Pediatric Endocrinology,
2015 - A homozygous nonsense TPO mutation R540X consistently causes congenital hypothyroidism in two siblings born to a consanguineous family
KARA CENGİZ. Journal of Clinical Research in Pediatric Endocrinology,
2015 - ASSOCIATION OF CONGENITAL ADRENAL HYPERPLASIA WITH AUTISM CASE REPORT
KARA CENGİZ. Journal of Clinical Research in Pediatric Endocrinology,
2015 - Association among vitamin B12 status obesity severity and metabolic syndrome in obese Turkish children
KARA CENGİZ. Journal of Clinical Research in Pediatric Endocrinology,
2015 - Growth curves for Turkish Girls with Turner Syndrome Results of the Turkish Turner Syndrome Study Group
DARENDELİLER FATMA FEYZA,YEŞİLKAYA EDİZ,BEREKET ABDULLAH,BAŞ FİRDEVS,BUNDAK RÜVEYDE,SARI ERKAN,AYDIN BANU,DARCAN ŞÜKRAN,DÜNDAR BUMİN NURİ,BÜYÜKİNAN MUAMMER,KARA CENGİZ,MAZICIOĞLU MUSTAFA MÜMTAZ,ADAL SERVET ERDAL,AKINCI AYŞEHAN,ATABEK MEHMET EMRE,DEMİREL FATMA,ÇELİK NURULLAH,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,ÖKTEN AYŞENUR,ABACI AYHAN,DÖNERAY HAKAN,ÖZBEK MEHMET NURİ,KESKİN MEHMET,ÖNAL HASAN,AKYÜREK NESİBE,BULAN KEZBAN,TEPE DERYA,EMEKSİZ HAMDİ CİHAN,DEMİR KORCAN,ÖZALP KIZILAY DENİZ,TOPALOĞLU ALİ KEMAL,EREN ERDAL,ÖZEN SAMİM,DEMİRBİLEK HÜSEYİN,ABALI SAYGIN,AKIN LEYLA,SELVER EKLİOĞLU BERAY,KABA SULTAN,ANIK AHMET,BAŞ SERPİL,ÜNÜVAR TOLGA,SAĞLAM HALİL,BOLU SEMİH,ÖZGEN İLKER TOLGA,DOĞAN DURMUŞ,ÇAKIR ESRA DENİZ,ŞEN YAŞAR,ANDIRAN NESİBE,ÇİZMECİOĞLU FİLİZ MİNE,EVLİYAOĞLU SAADET OLCAY,KARAGÜZEL GÜLAY,PİRGON MUSTAFA ÖZGÜR,ÇATLI GÖNÜL,CAN HATİCE DİLEK,GÜRBÜZ FATİH,BİNAY ÇİĞDEM,BAŞ VEYSEL,SAĞLAM CELAL,GÜL DAVUT,POLAT ADEM,AÇIKEL CENGİZHAN,CİNAZ PEYAMİ. Journal of Clinical Research in Pediatric Endocrinology, 7(3), 183-191.
2015 - Turner Syndrome and Associated Problems in Turkish Children A Multicenter Study
EDİZ YEŞİLKAYA,BEREKET ABDULLAH,DARENDELİLER FATMA FEYZA,BAŞ FİRDEVS,POYRAZOĞLU ŞÜKRAN,AYDIN KÜÇÜKEMRE BANU,DARCAN ŞÜKRAN,DÜNDAR BUMİN NURİ,MUAMMER BÜYÜKİNAN,KARA CENGİZ,SARI ERKAN,ADAL SERVET ERDAL,AKINCI AYŞEHAN,ATABEK MEHMET EMRE,DEMİREL FATMA,ÇELİK NURULLAH,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,AYŞENUR ÖKTEN,ABACI AYHAN,DÖNERAY HAKAN,MEHMET NURİ ÖZBEK,KESKİN MEHMET,ÖNAL HASAN,AKYÜREK NESİBE,KEZBAN BULAN,DERYA TEPE,EMEKSİZ HAMDİ CİHAN,ÖZALP KIZILAY DENİZ,TOPALOĞLU ALİ KEMAL,EREN ERDAL,ÖZEN SAMİM,ABALI SAYGIN,AKIN LEYLA,BERAY SELVER EKLİOĞLU,KABA SULTAN,ANIK AHMET,BAŞ SERPİL,ÜNÜVAR TOLGA,SAĞLAM HALİL,BOLU SEMİH,ÖZGEN İLKER TOLGA,DURMUŞ DOĞAN,ESRA DENİZ ÇAKIR,ŞEN YAŞAR,ANDIRAN NESİBE,ÇİZMECİOĞLU FİLİZ MİNE,EVLİYAOĞLU SAADET OLCAY,KARAGÜZEL GÜLAY,PİRGON MUSTAFA ÖZGÜR,ÇATLI GÖNÜL,CAN HATİCE DİLEK,GÜRBÜZ FATİH,ÇİĞDEM BİNAY,BAŞ VEYSEL NİJAT,FİDANCI KÜRŞAT,POLAT ADEM,AÇIKEL CENGİZHAN,DEMİRBİLEK HÜSEYİN,GÜL DAVUT,CİNAZ PEYAMİ,BONDY CAROLYN. Journal of Clinical Research in Pediatric Endocrinology, 7(1), 27-36.
2015 - Current Practice in Diagnosis and Treatment of Growth Hormone Deficiency in Childhood A Survey from Turkey
POYRAZOĞLU ŞÜKRAN,TEOMAN AKÇAY,ARSLANOĞLU İLKNUR,ATABEK MEHMET EMRE,ATAY ZEYNEP,BERBEROĞLU MERİH,BEREKET ABDULLAH,BİDECİ AYSUN,BİRCAN İFFET,BÖBER ECE,CAN ŞULE,CESUR YAŞAR,DARCAN ŞÜKRAN,DEMİR KORCAN,DÜNDAR BUMİN NURİ,ERSOY BETÜL,ESEN İHSAN,GÜVEN AYLA,KARA CENGİZ,KESKİN MEHMET,KURTOĞLU SELİM,NİHAL MEMİOĞLU,MEHMET NURİ ÖZBEK,ÖZGEN İLKER TOLGA,SARI ERKAN,ŞIKLAR ZEYNEP,ŞİMŞEK ENVER,TURAN SERAP,EDİZ YEŞİLKAYA,YÜKSEL BİLGİN,DARENDELİLER FATMA FEYZA. Journal of Clinical Research in Pediatric Endocrinology, 7(1), 37-44.
2014 - Premature ovarian failure due to tetrasomy X in an adolescent girl
KARA CENGİZ,ÜSTYOL ALA,YILMAZ AYŞEGÜL,ALTUNDAĞ ENGİN,OĞUR METHİYE GÖNÜL. European Journal of Pediatrics, 173(12), 1627-1630.
2014 - Vitamin D Intoxication Due to an Erroneously Manufactured Dietary Supplement in Seven Children
KARA CENGİZ,FİGEN GÜNİNDİ,ÜSTYOL ALA,AYDIN HASAN MURAT. PEDIATRICS, 133(1), 240-244.
2013 - Diabetes Care Glycemic Control Complications and Concomitant Autoimmune Diseases in Children with Type 1 Diabetes in Turkey A Multicenter Study
GÖKŞEN ŞİMŞEK RUHSAR DAMLA,AYCAN ZEHRA,ÖZEN SAMİM,ÇETİNKAYA SEMRA,KARA CENGİZ,ABALI SAYGIN,DEMİR KORCAN,TUNÇ ÖZGÜL,UÇAKTÜRK AHMET,GÜLGÜN ASAR,BAŞ FİRDEVS,ÇETİNKAYA ERGUN,AYDIN HASAN MURAT,KARAGÜZEL GÜLAY,ORBAK ZERRİN,ŞIKLAR ZEYNEP,ALTINCIK AYŞE,ÖKTEN AYŞENUR,ÖZKAN BEHZAT,ÖÇAL GÖNÜL,SEMİZ SERAP,ARSLANOĞLU İLKNUR,EVLİYAOĞLU SAADET OLCAY,BUNDAK RÜVEYDE,DARCAN ŞÜKRAN. Journal of Clinical Research in Pediatric Endocrinology, 5(1), 20-26.
2012 - Iodine deficiency in pregnant women in the apparently iodine sufficient capital city of Turkey
OĞUZ KUTLU ALEV,KARA CENGİZ. Clinical Endocrinology, 77(4), 615-620.
2012 - Myelofibrosis associated with rickets in a child with down syndrome
ALBAYRAK CANAN,ALBAYRAK DAVUT,KILINÇ AYŞE,KARA CENGİZ. Pediatric Blood & Cancer, 58(4), 647-648.
2011 - The effect of glucocorticoid replacement therapy on bone mineral density in children with congenital adrenal hyperplasia
ÇETİNKAYA SEMRA,KARA CENGİZ. J Pediatr Endocrinol Metab, 24(5-6), 265-269.
2011 - Etiological Classification and Clinical Assessment of Children and Adolescents with Disorders of Sex Development Original Article
ERDOĞAN SEMA,KARA CENGİZ,UÇAKTÜRK AHMET,AYDIN HASAN MURAT. journal of Clinical Research in Pediatric Endocrinology, 3(2), 77-83.
2011 - Rhabdomyolysis Without Detectable Myoglobulinuria Due to Severe Hypophosphatemia in Diabetic Ketoacidosis
OĞUZ KUTLU ALEV,KARA CENGİZ,ÇETİNKAYA SEMRA. Pediatric Emergency Care, 27(6), 537-538.
2010 - Adverse Effect of Phenytoin on Glucocorticoid Replacement in a Child with Adrenal Insufficiency
KARA CENGİZ,UÇAKTÜRK AHMET,AYDIN ÖMER FARUK,AYDIN HASAN MURAT. J Pediatr Endocrinol Metab, 23(9), 963-966.
2010 - Congenital goitrous hypothyroidism deafness and Iodide organification defect in four siblings Pendred or pseudo pendred syndrome
KARA CENGİZ,KILIÇ MEHTAP,UÇAKTÜRK AHMET,AYDIN HASAN MURAT. Journal of Clinical Research in Pediatric Endocrinology, 2(2), 81-84.
2010 - Response to the letter by Drs Vanden Eijnden and Martinovici
ÇETİNKAYA SEMRA,KUNAK BENAL,KARA CENGİZ,DEMİRÇEKEN FULYA,YARALI NEŞE,POLAT EMİNE,AYCAN ZEHRA. J Pediatr Endocrinol Metab, 23(11), 1208-1208.
2010 - A Case Report of Neonatal Diabetes due to Neonatal Hemochromatosis
ÇETİNKAYA SEMRA,KUNAK BENAL,KARA CENGİZ,DEMİRÇEKEN FULYA,YARALI NEŞE,POLAT EMİNE,AYCAN ZEHRA. J Pediatr Endocrinol Metab, 23(5), 521-524.
2009 - Postnatal testicular regression mircopenis and microcephaly Conformation of a new syndrome
OĞUZ KUTLU ALEV,AKBIYIK FATİH,KARA CENGİZ. American Journal of Medical Genetics Part A, 149(4), 742-745.
2008 - The effects of metabolic control on oxidized low density lipoproteinantibodies in children and adolescents with type 1 diabetes mellitus
KARA CENGİZ,ÇETİNKAYA SEMRA,SEZGİN NURZEN,KINIK SİBEL. PEDIATRIC DIABETES, 9(1), 17-22.
2008 - Incidence of iodine deficiency in Turkish patients with congenital hypothyroidism
EVLİYAOĞLU SAADET OLCAY,OĞUZ KUTLU ALEV,KARA CENGİZ,ATAVCI SEVİL. Pediatrics International, 50(3), 276-280.
2008 - Identification of Frequency and Distribution of the 9 Most Frequent Mutations among Patients with 21 OHD in Turkey
SADEGHİ FAEGHEH,YÜRÜR KUTLAY NİLGÜN,BERBEROĞLU MERİH,ERGUN ÇETİNKAYA,AYCAN ZEHRA,KARA CENGİZ,ILGIN RUHİ,ÖÇAL GÖNÜL,ŞIKLAR ZEYNEP,ELHAN ATİLLA HALİL,TÜKÜN FATMA AJLAN. J Pediatr Endocrinol Metab, 21(8), 781-787.
2008 - A case with homozygote familial hypercholesterolemia treated with LDL apheresis and coronary bypass in adolescence period
ALTINEL ESMA,ÇETİNKAYA SEMRA,KARA CENGİZ,ÖRÜN UTKU ARMAN,AYDIN HAKAN,KUTSAL ALİ. Anadolu Kardiyoloji Dergisi, 8(4), 231-232.
2008 - Persistently raised TSH in adequatly treated congenital hypothyroidism followed up for a long time
KARA CENGİZ,ÖCAL GÖNÜL,BERBEROĞLU MERİH,ŞIKLAR ZEYNEP,ADIYAMAN PELİN. J Pediatr Endocrinol Metab. 2008;21(3):251-6, 21(3), 251-256.
2008 - The effects of metabolic control on oxidized low density lipoprotein antibodies in children and adolescents with type 1 diabetes mellitus
KARA CENGİZ,ÇETİNKAYA SEMRA,SEZGİN NURZEN,KINIK SİBEL. Pediatric Diabetes, 9(1), 17-22.
2007 - Bilateral basal ganglia lesions after hypoglycemic coma in a 6 year old child
KARA CENGİZ,AYDIN ÖMER FARUK,ASLAN BELMA,GÜRER YAVUZ. J Child Neurol, 22(2), 228-231.
2005 - Sertoli cell tumor causing prepubertal gynecomastia in a boy with Peutz Jeghers syndrome The outcome of 1 year treatment with aromatase inhibitor testolactone
KARA CENGİZ,OĞUZ KUTLU ALEV,TOSUN MAHYA,APAYDIN SEMA,ŞENEL FERDA. Hormone Research, 63(5), 252-256.
2005 - Successful treatment of insulin allergy in a 1 year old infant with neonatal diabetes by lispro and glargine insulin
KARA CENGİZ,OĞUZ KUTLU ALEV,EVLİYAOĞLU SAADET OLCAY,BİLGİLİ HATİCE,YILDIRIM NURDAN. Diabetes Care 2005, 28(4), 983-984.
2003 - Alpha 1 antityripsin deficiency an overlooked cause of late hemorrhagic disease of the newborn
SİPAHİ TANSU,KARA CENGİZ,TAVİL EMİNE BETÜL,İNCİ AYŞE,OKSAL AYŞEGÜL. J Pediatr Hematol Onkol, 25(3), 274-275.
2001 - Spondylocostal Dysostosis Presentation of Two Cases
KARAKURT CEMŞİT,KARA CENGİZ,AKGÜN DENİZ,SİPAHİ TANSU. Int Pediatr, 16(3), 173-175.
2001 - Successful treatment of visceral leishmaniasis with allopurinol plus ketoconasole in an infant who developed pancreatitis caused by meglumine antimonate
KUYUCU NECDET,KARA CENGİZ,BAKIRTAŞ ARZU,TEZİÇ TAHSİN. Pediatr Infect Dis J, 20(4), 455-457.
Lange-Current Tanı ve Tedavi Pediatri
2018 - Türkçe, Kitap Tercümesi
ISBN: 978-60567905-1-5
SAVAŞ ERDEVE ŞENAY,hacıhamdioglu bülent,KARA CENGİZ,catlı gönül
Yurdakök PEDİATRİ
2017 - Türkçe, Bilimsel Kitap
ISBN: 978-975-277-663-0
AYDIN HASAN MURAT,KARA CENGİZ
YURDAKÖK PEDİATRİ
2017 - Türkçe, Bilimsel Kitap
ISBN: 978-975-277-663-0
AYDIN HASAN MURAT,KARA CENGİZ
Cinsiyet Gelişim Bozuklukları
2015 - Türkçe, Bilimsel Kitap
ISBN:
AYDIN HASAN MURAT,KARA CENGİZ
"Comparison of Triptorelin Versus Leuprolide inTreatment of Girls with Central Precocious Puberty", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi",
(2016), "3 Beta hidroksisteroid dehidrogenaz 2 eksikliği olan hastalarda klinik genetik ve steroid metabolom özelliklerinin araştırılması", "Ulusal", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi",
(2018), "Türkiye`de Konjenital Adrenal Hiperplazi Yenidoğan Taraması: 38.936 Bebeği Kapsayan Pilot Çalışma Verilerinin Değerlendirilmesi", "Ulusal", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi",
(2017), "Association of developmental delay, congenital adrenal hypoplasia, duchenne muscular dystrophy and glycerol kinase deficiency: a rare Xp21 contiguous gene deletion syndrome", "Ulusal", "Sağlık Bilimleri Temel Alanı>Çocuk Genetik Hastalıkları", "2139-2247",
(2018), "Neonatal Screening for Congenital AdrenalHyperplasia in Turkey: A Pilot Study with 38,935Infants", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi", "10.1159/000492307",
(2015), "Utility of Estimated Glucose Disposal Rate and Fat Mass Percentage for Predicting Metabolic Syndrome in Children and Adolescents with Type 1 Diabetes", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi",
(2018), "Nationwide Hypophosphatemic Rickets Study", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi", "10.1159/000492307", "1663-2818",
(2018), "Mutation spectrum of GCK, HNF1A and HNF1B in MODY patients and 40 novel mutations. May 27–30, 2017, Copenhagen, Denmark.", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Sağlığı ve Hastalıkları",
(2017), "MODY Sendromlarından Sorumlu GCK, HNF1A VE HNF1B Genleri Mutasyon Spektrumu ve 40 Yeni Mutasyon", "Ulusal", "Sağlık Bilimleri Temel Alanı->Çocuk Sağlığı ve Hastalıkları",
(2018), "Nationwide Hypophosphatemic Rickets Study", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Sağlığı ve Hastalıkları", " 10.1159/000492307", "1663-2826",
(2018), "Çok Merkezli Olarak Hipofosfatemik Riketsli Olguların Değerlendirilmesi", "Ulusal", "Sağlık Bilimleri Temel Alanı->Çocuk Sağlığı ve Hastalıkları",
(2018), "17OH-Pregnenolone seems a major drive of androgen excess in patients with 11ß-hydroxylase deficiency", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi",
(2018), "Evaluation of molecular characteristics and steroid metabolomics in a large cohort of children with 3β-Hydroxysteroid Dehydrogenase 2 deficiency.", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi",
(2018), "Nationwide Hypophosphatemic Rickets Study", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi", "10.1159/000492307",
(2018), "Neonatal Screening for Congenital AdrenalHyperplasia in Turkey: A Pilot Study with 38,935Infants", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi", "10.1159/000492307",
(2018), "Neonatal Screening for Congenital AdrenalHyperplasia in Turkey: A Pilot Study with 38,935Infants", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi", "10.1159/000492307",
(2018), "Neonatal screening for congenital adrenal hyperplasia in Turkey: A pilot study with 38935 infants", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Sağlığı ve Hastalıkları",
"Türkiyede Konjenital Adrenal Hiperplazi Yenidoğan Taraması", "Ulusal", "Sağlık Bilimleri Temel Alanı->Çocuk Sağlığı ve Hastalıkları",
(2017), "PHENOTYPIC, HORMONAL AND MOLECULAR GENETIC CHARACTERISTICS OF 5-ALPHA REDUCTASE TYPE 2 DEFICIENCY PATIENTS: A MULTICENTER STUDY FROM TURKEY.", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi",
"Çok Merkezli Olarak Hipofosfatemik Riketsli Olguların Değerlendirilmesi", "Ulusal", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi",
(2018), "5-Alfa Redüktaz Tip 2 Eksikliği Tanılı Olguların Fenotipik, Hormonal veMoleküler Genetik Özellikleri: Çok Merkezli Ulusal Veriler", "Ulusal", "Sağlık Bilimleri Temel Alanı->Çocuk Sağlığı ve Hastalıkları", "10.1007/s40618-018-0940-y",
"Çok Merkezli Olarak Hipofosfatemik Riketsli Olguların Değerlendirilmesi", "Ulusal", "Sağlık Bilimleri Temel Alanı->Çocuk Sağlığı ve Hastalıkları",
"Nationwide Hypophosphatemic Rickets Study", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Sağlığı ve Hastalıkları",
(2018), "PHENOTYPIC, HORMONAL AND MOLECULAR GENETIC CHARACTERISTICS OF 5-ALPHA REDUCTASE TYPE 2 DEFICIENCY PATIENTS: AMULTICENTER STUDY FROM TURKEY", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Sağlığı ve Hastalıkları", ": 10.1007/s40618-018-0940-y",
(2017), "Williams Syndrome Associated with Isolated Growth Hormone Deficiency: Is It Just a Coincidence?", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Tıbbi Genetik",
(2017), "5-alfa redüktaz tip 2 eksikliği tanılı olguların fenotipik, hormonal ve moleküler genetik özellikleri: Çok merkezli ulusal veriler", "Ulusal", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi",
(2017), "MODY Sendromlarından Sorumlu GCK, HNF1A ve HNF1B Genleri Mutasyon Spektrumu ve 40 Yeni Mutasyon", "Ulusal", "Sağlık Bilimleri Temel Alanı->Tıbbi Genetik",
(2015), "Obezite", "Ulusal", "Sağlık Bilimleri Temel Alanı->Çocuk Sağlığı ve Hastalıkları",
(2015), "Aetiological Spectrum and Clinical Characteristics of 129 Children with Gonadotropin Independent Precocious Puberty A Nationwide Cohort Study", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi",
(2015), "The Growth Characteristics of Patients with Noonan Syndrome and First 2 Years Results of GH Treatment A Nationwide Multicentre Study", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi",
(2015), "Primary Adrenal Insufficiency in Children without Congenital Adrenal Hyperplasia Molecular and Clinical Characterisation of a Nationwide Cohort", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi",
(2015), "Current Practice in Diagnosis and Treatment of GHDeficiency in Childhood A Survey from Turkey", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi",
(2015), "Growth Curves for Turkish Girls with Turner Syndrome Results of the Turkish Turner Syndrome Study Group", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi",
(2015), "Anthropometric Findings from Birth to Adulthood in Turkish Girls with Turner Syndrome and Association with Karyotpye Distribution", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi",
(2015), "Comparison of Treatment Alternatives for Hypercalcemia due to Vitamin D Intoxication in Children", "Uluslararası", "Sağlık Bilimleri Temel Alanı->Çocuk Endokrinolojisi",