Prof. Dr. Cengiz Kara

Prof. Dr. Cengiz Kara 1985 yılında Ankara Lisesi’nden, 1991 yılında ise Ankara Üniversitesi Tıp Fakültesinden mezun oldu. Çocuk Sağlığı ve Hastalıkları uzmanlık eğitimini 1996 yılında ve Çocuk Endokrinolojisi yan dal uzmanlık eğitimini 2005 yılında Dr. Sami Ulus Çocuk Hastanesinde tamamlamasının ardından, 2007 yılında Ondokuz Mayıs Üniversitesine Yrd. Doç. Dr. olarak atandı. Dr. Kara 2010 yılında doçent ve 2016 yılında profesör unvanlarını aldı. Dr. Kara fakülte görevleri yanı sıra 2021 yılında Ondokuz Mayıs Üniversitesi Lisansüstü Eğitim Enstitüsü Moleküler Tıp programında doktorasını (PhD) t...

Makaleler

Does Type 1 Diabetes Mellitus Affect the Shear Wave Velocity of the Thyroid Gland of Children Without Autoimmune Thyroiditis? , 2017
Acoustic Radiation Force Impulse Imaging in the Differential Diagnosis of an Ectopic Intrathyroidal Thymus , 2017
Revisiting Classical 3β-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric Cases , 2020
Adverse Effect of Phenytoin on Glucocorticoid Replacement in a Child with Adrenal Insufficiency , 2010
Utility of estimated glucose disposal rate for predicting metabolic syndrome in children and adolescents with type-1 diabetes , 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 , 2020
Transient Neonatal Diabetes with Fanconi Bickel Syndrome , 2017
Acoustic Radiation Force Impulse Quantification in the Evaluation of Thyroid Elasticity in Pediatric Patients With Hashimoto Thyroiditis , 2018
Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants , 2019
Myelofibrosis associated with rickets in a child with down syndrome , 2012
Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 Infants , 2020
Transient Neonatal Diabetes with Fanconi Bickel Syndrome , 2016
Comparison of Treatment Regimens for the Management of Severe Hypercalcemia due to Vitamin D Intoxication in Children , 2018
Nationwide hypophosphatemic rickets study57th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE) , 2018
Gebelikte tiroid hastalıklarının neonatal etkileri ve TSH yüksekliği olan bebeğe yaklaşım: Türk Neonatoloji ve Çocuk Endokrinoloji ve Diabet Dernekleri Uzlaşı Raporu , 2018
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 , 2019
Analysis of the GCK gene in 79 MODY type 2 patients: A multicenter Turkish study, mutation profile and description of twenty novel mutations , 2018
Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants. , 2018
Role of Point Shear Wave Elastography in the Determination of the Severity of Fibrosis in Pediatric Liver Diseases With Pathologic Correlations , 2017
Pubertenin Epigenetik Kontrolü , 2016
Multisystemic Severe Form Pseudohypoaldosteronism Can Gastrostomy be Useful in the Management , 2016
The Growth Characteristics of Patients with Noonan Syndrome Results of Three Years of Growth Hormone Treatment A Nationwide Multicenter Study , 2016
The Etiology and Clinical Features of Non CAH Gonadotropin Independent Precocious Puberty A Multicenter Study , 2016
Evaluation of therapeutics management patterns and glycemic control of pediatric type 1 diabetes mellitus patients in Turkey A nationwide cross sectional study , 2016
Transient Congenital Hypothyroidism in Turkey An Analysis on Frequency and Natural Course , 2016
The effects of metabolic control on oxidized low density lipoproteinantibodies in children and adolescents with type 1 diabetes mellitus , 2008
Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome , 2016
Efficacy and safety of pamidronate in children with vitamin D intoxication , 2016
Spondylocostal Dysostosis Presentation of Two Cases , 2001
Incidence of iodine deficiency in Turkish patients with congenital hypothyroidism , 2008
Identification of Frequency and Distribution of the 9 Most Frequent Mutations among Patients with 21 OHD in Turkey , 2008
A case with homozygote familial hypercholesterolemia treated with LDL apheresis and coronary bypass in adolescence period , 2008
Diabetes Care Glycemic Control Complications and Concomitant Autoimmune Diseases in Children with Type 1 Diabetes in Turkey A Multicenter Study , 2013
Iodine deficiency in pregnant women in the apparently iodine sufficient capital city of Turkey , 2012
Myelofibrosis associated with rickets in a child with down syndrome , 2012
The effect of glucocorticoid replacement therapy on bone mineral density in children with congenital adrenal hyperplasia , 2011
Congenital goitrous hypothyroidism deafness and Iodide organification defect in four siblings Pendred or pseudo pendred syndrome , 2010
Etiological Classification and Clinical Assessment of Children and Adolescents with Disorders of Sex Development Original Article , 2011
Rhabdomyolysis Without Detectable Myoglobulinuria Due to Severe Hypophosphatemia in Diabetic Ketoacidosis , 2011
Bilateral basal ganglia lesions after hypoglycemic coma in a 6 year old child , 2007
Sertoli cell tumor causing prepubertal gynecomastia in a boy with Peutz Jeghers syndrome The outcome of 1 year treatment with aromatase inhibitor testolactone , 2005
Successful treatment of insulin allergy in a 1 year old infant with neonatal diabetes by lispro and glargine insulin , 2005
Successful treatment of visceral leishmaniasis with allopurinol plus ketoconasole in an infant who developed pancreatitis caused by meglumine antimonate , 2001
Alpha 1 antityripsin deficiency an overlooked cause of late hemorrhagic disease of the newborn , 2003
Postnatal testicular regression mircopenis and microcephaly Conformation of a new syndrome , 2009
Persistently raised TSH in adequatly treated congenital hypothyroidism followed up for a long time , 2008
The effects of metabolic control on oxidized low density lipoprotein antibodies in children and adolescents with type 1 diabetes mellitus , 2008
Response to the letter by Drs Vanden Eijnden and Martinovici , 2010
A Case Report of Neonatal Diabetes due to Neonatal Hemochromatosis , 2010
Association between autoimmune thyroid diseases and Neurofibromatosis type 1 is endocrinological evaluation necessary for children with Neurofibromatosis type 1 , 2015
A homozygous nonsense TPO mutation R540X consistently causes congenital hypothyroidism in two siblings born to a consanguineous family , 2015
ASSOCIATION OF CONGENITAL ADRENAL HYPERPLASIA WITH AUTISM CASE REPORT , 2015
Association among vitamin B12 status obesity severity and metabolic syndrome in obese Turkish children , 2015
Growth curves for Turkish Girls with Turner Syndrome Results of the Turkish Turner Syndrome Study Group , 2015
Turner Syndrome and Associated Problems in Turkish Children A Multicenter Study , 2015
Premature ovarian failure due to tetrasomy X in an adolescent girl , 2014
Vitamin D Intoxication Due to an Erroneously Manufactured Dietary Supplement in Seven Children , 2014
Current Practice in Diagnosis and Treatment of Growth Hormone Deficiency in Childhood A Survey from Turkey , 2015

Bildiriler

Nationwide Hypophosphatemic Rickets Study - ŞIKLAR ZEYNEP,Turan Serap,BEREKET ABDULLAH,ABACI AYHAN,BAŞ FİRDEVS,DEMİR KORCAN,Guran Tulay,AKBERZADE AZAD,BÖBER ECE,Özbek Mehmet Nuri,KARA CENGİZ,POYRAZOĞLU ŞÜKRAN,AYDIN HASAN MURAT,KARDELEN ASLI,TARIM ÖMER FARUK,EREN ERDAL,HATİPOĞLU NİHAL,BÜYÜKİNAN MUAMMER,Akyürek Nesibe,ÇETİNKAYA SEMRA,BAYRAMOGLU ELVAN,Eklioğlu Beray Selver,UÇAKTÜRK AHMET,ABALI SAYGIN,GÖKŞEN ŞİMŞEK RUHSAR DAMLA,Kör Yılmaz,Ünal Edip,ESEN İHSAN,YILDIRIM RUKEN,AKIN ONUR,ÇAYIR ATİLLA,DİLEK EMİNE,KIREL BİRGÜL,ANIK AHMET,ÇATLI GÖNÜL,BERBEROĞLU MERİH
Comparison of Triptorelin Versus Leuprolide inTreatment of Girls with Central Precocious Puberty - CAN YILMAZ GÜLAY,KARA CENGİZ,ÇELEBİ BİTKİN EDA,AYDIN HASAN MURAT
3 Beta hidroksisteroid dehidrogenaz 2 eksikliği olan hastalarda klinik genetik ve steroid metabolom özelliklerinin araştırılması - GÜRAN TÜLAY, KARA CENGİZ, ATAY ZEYNEP, AKBARZADE AZAD, CAN YILMAZ GÜLAY, ÇELEBİ BİTKİN EDA, AKÇAY TEOMAN, YILDIZ MELEK, GÜVEN AYLA, ÇATLI GÖNÜL, YEŞİL SAYIN GÖZDE, BAŞ SERPİL, HAKLAR GONCAGÜL, ŞİRİKÇİ ÖNDER, turan serap, BEREKET ABDULLAH
Türkiye`de Konjenital Adrenal Hiperplazi Yenidoğan Taraması: 38.936 Bebeği Kapsayan Pilot Çalışma Verilerinin Değerlendirilmesi - 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
Association of developmental delay, congenital adrenal hypoplasia, duchenne muscular dystrophy and glycerol kinase deficiency: a rare Xp21 contiguous gene deletion syndrome - ALTUNDAĞ ENGİN,KARA CENGİZ,SANRI ASLIHAN,MUTLU ALBAYRAK HATİCE,YALÇIN HATİCE YELDA,OĞUR METHİYE GÖNÜL
Neonatal Screening for Congenital AdrenalHyperplasia in Turkey: A Pilot Study with 38,935Infants - 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
Utility of Estimated Glucose Disposal Rate and Fat Mass Percentage for Predicting Metabolic Syndrome in Children and Adolescents with Type 1 Diabetes - KÖKEN ÖZLEM,KARA CENGİZ,CAN YILMAZ GÜLAY,AYDIN HASAN MURAT
Nationwide Hypophosphatemic Rickets Study - 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
Mutation spectrum of GCK, HNF1A and HNF1B in MODY patients and 40 novel mutations. May 27–30, 2017, Copenhagen, Denmark. - ÖZKINAY FERİŞTAH FERDA,IŞIK ESRA,GÖKŞEN ŞİMŞEK RUHSAR DAMLA,AYKUT AYÇA,KARACA EMİN,ÖZEN SAMİM,BOLAT HİLMİ,ATİK TAHİR,SAYGILI LÜTFİYE FÜSUN,KARTAL E,GUL U,ANIK AHMET,TÜTÜNCÜLER FİLİZ,EREN ERDAL,Özbek Mehmet Nuri,BÖBER ECE,ABACI AYHAN,KIREL BİRGÜL,ERSOY BETÜL,BÜYÜKİNAN MUAMMER,KARA CENGİZ,ÇAKIR ESRA PAPATYA,YILDIRIM RUKEN,İŞGÜVEN ŞÜKRİYE PINAR,DAĞDEVİREN A,AGLADIOGLU SEBAHAT YILMAZ,DOĞAN MURAT,SANGÜN ÖZLEM,ARSLANOĞLU İLKNUR,Korkmaz Hüseyin Anıl,TEMİZ FATİH,ONAY HÜSEYİN
MODY Sendromlarından Sorumlu GCK, HNF1A VE HNF1B Genleri Mutasyon Spektrumu ve 40 Yeni Mutasyon - ÖZKINAY FERİŞTAH FERDA,IŞIK ESRA,GÖKŞEN ŞİMŞEK RUHSAR DAMLA,AYKUT AYÇA,KARACA EMİN,ÖZEN SAMİM,BOLAT HİLMİ,ATİK TAHİR,SAYGILI FİSUN,KARTAL EMİNE,ÜLKÜ GÜL,ANIK AHMET,TÜTÜNCÜLER FİLİZ,EREN ERDAL,Özbek Mehmet Nuri,BÖBER ECE,ABACI AYHAN,KIREL BİRGÜL,ERSOY BETÜL,BÜYÜKİNAN MUAMMER,ÇETİNKALP ŞEVKİ,KARA CENGİZ,ÇAKIR ESRA PAPATYA,YILDIRIM RUKEN,İŞGÜVEN ŞÜKRİYE PINAR,AĞLADIOĞLU SEBAHAT YILMAZ,DOĞAN MURAT,SANGÜN ÖZLEM,ARSLANOĞLU İLKNUR,Korkmaz Hüseyin Anıl,TEMİZ FATİH,ONAY HÜSEYİN
Çok Merkezli Olarak Hipofosfatemik Riketsli Olguların Değerlendirilmesi - ŞIKLAR ZEYNEP,Turan Serap,BEREKET ABDULLAH,ABACI AYHAN,Guran Tulay,DEMİR KORCAN,Akberzede Azad,BAŞ FİRDEVS,BÖBER ECE,Özbek Mehmet Nuri,KARA CENGİZ,POYRAZOĞLU ŞÜKRAN,Aydın Murat,Kardelen Aslı,TARIM ÖMER FARUK,EREN ERDAL,HATİPOĞLU NİHAL,BÜYÜKİNAN MUAMMER,Akyürek Nesibe,ÇETİNKAYA SEMRA,Bayramoğlu Elvan,Eklioğlu Beray Selver,Uçaktürk Ahmet,ABALI SAYGIN,Goksen Damla,Kor Yılmaz,Ünal Edip,ESEN İHSAN,YILDIRIM RUKEN,AKIN ONUR,ÇAYIR ATİLLA,DİLEK EMİNE,KIREL BİRGÜL,ANIK AHMET,ÇATLI GÖNÜL,BERBEROĞLU MERİH
17OH-Pregnenolone seems a major drive of androgen excess in patients with 11ß-hydroxylase deficiency - 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
Evaluation of molecular characteristics and steroid metabolomics in a large cohort of children with 3β-Hydroxysteroid Dehydrogenase 2 deficiency. - 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
Nationwide Hypophosphatemic Rickets Study - 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
Neonatal Screening for Congenital AdrenalHyperplasia in Turkey: A Pilot Study with 38,935Infants - 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 - 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 adrenal hyperplasia in Turkey: A pilot study with 38935 infants - 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
Türkiyede Konjenital Adrenal Hiperplazi Yenidoğan Taraması - 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
PHENOTYPIC, HORMONAL AND MOLECULAR GENETIC CHARACTERISTICS OF 5-ALPHA REDUCTASE TYPE 2 DEFICIENCY PATIENTS: A MULTICENTER STUDY FROM TURKEY. - 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
Çok Merkezli Olarak Hipofosfatemik Riketsli Olguların Değerlendirilmesi - 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
5-Alfa Redüktaz Tip 2 Eksikliği Tanılı Olguların Fenotipik, Hormonal veMoleküler Genetik Özellikleri: Çok Merkezli Ulusal Veriler - 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
Çok Merkezli Olarak Hipofosfatemik Riketsli Olguların Değerlendirilmesi - 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
Nationwide Hypophosphatemic Rickets Study - 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
PHENOTYPIC, HORMONAL AND MOLECULAR GENETIC CHARACTERISTICS OF 5-ALPHA REDUCTASE TYPE 2 DEFICIENCY PATIENTS: AMULTICENTER STUDY FROM TURKEY - 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
Williams Syndrome Associated with Isolated Growth Hormone Deficiency: Is It Just a Coincidence? - OĞUR METHİYE GÖNÜL,KARA CENGİZ,YALÇIN HATİCE YELDA,YILMAZ AYŞEGÜL,ALTUNDAĞ ENGİN,ABUR ÜMMET,BAYSAL MEHMET KEMAL,AYDIN HASAN MURAT
5-alfa redüktaz tip 2 eksikliği tanılı olguların fenotipik, hormonal ve moleküler genetik özellikleri: Çok merkezli ulusal veriler - 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
MODY Sendromlarından Sorumlu GCK, HNF1A ve HNF1B Genleri Mutasyon Spektrumu ve 40 Yeni Mutasyon - ÖZKINAY FERİŞTAH FERDA,IŞIK ESRA,GÖKŞEN ŞİMŞEK RUHSAR DAMLA,AYKUT AYÇA,KARACA EMİN,ÖZEN SAMİM,ATİK TAHİR,BOLAT HİLMİ,SAYGILI LÜTFİYE FÜSUN,KARTAL EMİNE,GÜL ÜLKÜ,ANIK AHMET,TÜTNCÜLER FİLİZ,EREN ERDAL,ÖZBEK MEHMET NURİ,BÖBER ECE,ABACI AYHAN,KIREL BİRGÜL,ERSOY BETÜL,BÜYÜKİNAN MUAMMER,ÇETİNKALP ŞEVKİ,KARA CENGİZ,PAPATYA ÇAKIR ESRA,YILDIRIM RUKEN,İŞGÜVEN PINAR,DAĞDEVİREN ÇAKIR AYDİLEK,YILMAZ AĞLADIOĞLU SEBAHAT,DOĞAN MURAT,SANGÜN ÖZLEM,ARSLANOĞLU İLKNUR,KORKMAZ H A,TEMİZ FATİH,ONAY HÜSEYİN
xx - KARA CENGİZ
Obezite - KARA CENGİZ
Aetiological Spectrum and Clinical Characteristics of 129 Children with Gonadotropin Independent Precocious Puberty A Nationwide Cohort Study - ATAY ZEYNEP,YEŞİLKAYA EDİZ,ERDEVE ŞENAY,AKIN LEYLA,EREN ERDAL,DÖGER ESRA,AYCAN ZEHRA,YAVAŞ ABALI ZEHRA,AKINCI AYŞEHAN,ŞIKLAR ZEYNEP,ÖZEN SAMİM,KARA CENGİZ,TAYFUN MELTEM,TÜTÜNCÜLER FİLİZ,KARAGÜZEL GÜLAY,SAĞLAM HALİL,BİDECİ AYSUN,KURTOĞLU SELİM,BEREKET ABDULLAH,TURAN SERAP,SARI ERKAN,ÇETİNKAYA SEMRA,GÜRAN TÜLAY
The Growth Characteristics of Patients with Noonan Syndrome and First 2 Years Results of GH Treatment A Nationwide Multicentre Study - ŞIKLAR ZEYNEP,BERBEROĞLU MERİH,GENENS MİKAYİR,POYRAZOĞLU ŞÜKRAN,BAŞ FİRDEVS,DARENDELİLER FATMA FEYZA,BUNDAK RÜVEYDE,AYCAN ZEHRA,ERDEVE ŞENAY,ÇETİNKAYA SEMRA,ABALI SAYGIN,ATAY ZEYNEP,TURAN SERAP,KARA CENGİZ,CAN YILMAZ GÜLAY,AKYÜREK NESİBE,ABACI AYHAN,SARI ERKAN,YEŞİLKAYA EDİZ,BOLU SEMİH,ŞİMŞEK ENVER,KORKMAZ HÜSEYİN ANIL,ÇATLI GÖNÜL,ÇAYIR ATİLLA,EVLİYAOĞLU SAADET OLCAY,İŞGÜVEN ŞÜKRİYE PINAR
Primary Adrenal Insufficiency in Children without Congenital Adrenal Hyperplasia Molecular and Clinical Characterisation of a Nationwide Cohort - BUONOCORE FEDERİCA,NURÇİN SAKA,ÖZBEK MEHMET NURİ,AYCAN ZEHRA,BEREKET ABDULLAH,BAŞ FİRDEVS,DARCAN ŞÜKRAN,BİDECİ AYSUN,TURAN SERAP,GÜVEN AYLA,TARIM ÖMER FARUK,AĞLADIOĞLU SABAHAT,ATAY ZEYNEP,ÖZEN SAMİM,DEMİR KORCAN,AKINCI AYŞEHAN,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,ABALI ZEHRA YAVAŞ,DOGER ESRA,EREN ERDAL,BERBEROĞLU MERİH,HACIHAMDİOĞLU BÜLENT,ACHERMANN JOHN C
Current Practice in Diagnosis and Treatment of GHDeficiency in Childhood A Survey from Turkey - 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
Growth Curves for Turkish Girls with Turner Syndrome Results of the Turkish Turner Syndrome Study Group - DARENDELİLER FATMA FEYZA,BEREKET ABDULLAH,BAŞ FİRDEVS,BUNDAK RÜVEYDE,SARI ERKAN,AYDIN KÜÇÜKEMRE 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,ŞİMŞEK ENVER,CİNAZ PEYAMİ
Anthropometric Findings from Birth to Adulthood in Turkish Girls with Turner Syndrome and Association with Karyotpye Distribution - SARI ERKAN,BEREKET ABDULLAH,YEŞİLKAYA EDİZ,BAŞ FİRDEVS,BUNDAK RÜVEYDE,KÜÇÜKEMRE AYDIN BANU,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,ERCAN OYA
Comparison of Treatment Alternatives for Hypercalcemia due to Vitamin D Intoxication in Children - DEMİR KORCAN,DÖNERAY HAKAN,YEŞİLKAYA EDİZ,KARA CENGİZ,ATAY ZEYNEP,ÇETİNKAYA SEMRA,ÇAYIR ATİLLA,ANIK AHMET,EREN ERDAL,DEMİREL FATMA,CAN YILMAZ GÜLAY,ERGÜR AYÇA,KENDİRCİ MUSTAFA,AYCAN ZEHRA,BEREKET ABDULLAH,AYDIN HASAN MURAT,ORBAK ZERRİN,ÖZKAN BEHZAT

Kitaplar

Lange-Current Tanı ve Tedavi Pediatri – Ema Tıp Kitabevi
Yurdakök PEDİATRİ – GÜNEŞ TIP KİTABEVLERİ
YURDAKÖK PEDİATRİ – GÜNEŞ TIP KİTAPEVLERİ
Cinsiyet Gelişim Bozuklukları – Nobel Tıp Kitapevleri

Prof. Dr. Cengiz Kara - İstinye Üniversitesi

cengiz.kara@istinye.edu.tr

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Sağlık Bilimleri Temel Alanı
Çocuk Endokrinolojisi (Çocuk Sağlığı ve Hastalıkları)

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