Long-term clinical outcomes of primary adrenal insufficiency caused by homozygous CYP11A1 p.R451W variant

Atilla Çayır, HÜSEYİN DEMİRBİLEK, Ilknur Kurt, Ayberk Turkyilmaz, Serkan Bilge Koca, Mehmet Nuri Ozbek, Murat Karaoglan, Hamdi Cihan Emeksiz, İSMAİL DÜNDAR, Esra DİŞÇİ, Ayse Sena Donmez, Gonul Catlı ve 6 yazar daha

• WoS Q1
• Scopus Q1

Genetic Analyses in a Cohort of Pediatric Patients with Congenital Hypothyroidism Based on Congenital Hypothyroidism Consensus Guideline

Erdal Kurnaz, AYBERK TÜRKYILMAZ, Oguzhan Yarali, Ayse Sena Doenmez, Atilla Çayır

• WoS Q1
• Scopus Q1
• WoS 2 atıf

Phenotypes Linked to Duplication Upstream of SOX9: New Insights Into Presentation and Diagnosis

Edip Unal, Aysel Tekmenuray-Unal, Atilla Çayır, Esra Deniz Papatya Cakir, Nurcan Beyazit, Baris Kolbasi, Busra Gurpinar Tosun, Gokhan Yigit, Arne Zibat, Bernd Wollnik, Huseyin Demirbilek, Tulay Guran

• WoS Q1
• Scopus Q1
• WoS 1 atıf

Gene Panel-Based Genotyping of 279 Turkish Maturity-Onset Diabetes of the Young Patients from Eastern Anatolia

Oguzhan Yarali, AYBERK TÜRKYILMAZ, Muharrem Bayrak, Mustafa Can Güler, Atilla Çayır

• WoS Q4
• Scopus Q4

The Course of Progranulin Levels at Admission and During Early Period of Insulin Treatment in Children with Newly Diagnosed Type 1 Diabetes Mellitus.

Ayse Sena Donmez, Atilla Çayır, Esra Laloğlu, Alev Lazoglu Ozkaya, Esra Dişci, Serap Kilic Kaya, Kamber Kaşali, Serkan Bilge Koca, Huseyin Demirbilek

• WoS Q2
• Scopus Q2

Responses of Different Artificial Intelligence Systems to Questions Related with Short Stature as Assessed by Pediatric Endocrinologists.

Kamber Kaşali, Özgür Fırat Özpolat, Merve Ülkü, Ayşe Sena Dönmez, Serap Kılıç Kaya, Esra Dişçi, Serkan Bilge Koca, Ufuk Özkaya, Hüseyin Demirbilek, Atilla Çayır

• WoS Q2
• Scopus Q2

Comparison of the clinical characteristics of children with Silver-Russell syndrome genetically confirmed or not and their response to growth hormone therapy: a national multicenter study

Ilker Tolga Ozgen, TUĞÇE KANDEMİR, MELEK YILDIZ, ŞÜKRAN POYRAZOĞLU, ZEYNEP ŞIKLAR, Nilay Sema Abseyi, Merih Berberoglu, Semra Cetinkaya, Senem Esen, Nursel Muratoglu Sahin, Sukran Darcan, Deniz Ozalp Kizilay ve 16 yazar daha

• WoS Q3
• Scopus Q2
• WoS 1 atıf

Genotype, Phenotype Characteristics and Long-Term Follow-Up of Patients with Vitamin D-Dependent Rickets Type IA: A Nationwide Multi-Centre Retrospective Cross-Sectional Study

Atilla Çayır, Hüseyin Demirbilek, Ayberk Türkyılmaz, Serap Demircioğlu, Abdullah Bereket, Feyza Darendeliler, Mehmet Nuri Özbek, Serkan Bilge Koca, Edip Unal, Deniz Okdemir, Ihsan Esen, Erdal Eren ve 22 yazar daha

• WoS Q1
• Scopus Q1
• WoS 1 atıf

Key Clinical and X-Ray Characteristics for the Diagnosis of Kenny-Caffey Syndrome Types 1 and 2

ENVER ŞİMŞEK, Sumeyye Emel Eren, Atilla Çayır, Oguzhan Tokur, OĞUZ ÇİLİNGİR, TÜLAY ŞİMŞEK

• WoS Q4
• Scopus Q4
• WoS 3 atıf

Diabetes Insipidus as an Early Clinical Indicator of Wolfram Syndrome Type 1: Evidence From a Symptom-Based Screening Approach

Ozge Beyza Gundogdu Ogutlu, Atilla Çayır, Ayse Sena Donmez, Serkan Bilge Koca, Oguzhan Yarali, HÜSEYİN DEMİRBİLEK

• WoS Q2
• Scopus Q1

Clinical and genetic characteristics of patients with monocarboxylate transporter-8 deficiency: a multicentre retrospective study

NURULLAH ÇELİK, KORCAN DEMİR, Saime Ergen Dibeklioglu, Bumin Nuri Dundar, NİHAL HATİPOĞLU, Gul Yesiltepe Mutlu, EMRULLAH ARSLAN, Didem Yildirimcakar, Atilla Çayır, Bulent Hacihamdioglu, Zumrut Kocabey Sutcu, Yagmur Unsal ve 1 yazar daha

• WoS Q1
• Scopus Q1
• WoS 3 atıf

Natural history of ENPP1 deficiency: Nationwide Turkish Cohort Study of autosomal-recessive hypophosphataemic rickets type 2

Fatma Dursun, İHSAN TURAN, Eda celebi Bitkin, Elvan BAYRAMOĞLU, Atilla Çayır, Senay Savas Erdeve, Esra Deniz Papatya Cakir, EMİNE ÇAMTOSUN, Semine Ozdemir Dilek, Heves Kirmizibekmez, Metin Eser, Ayberk Turkyilmaz ve 1 yazar daha

• WoS Q3
• Scopus Q2
• WoS 5 atıf

Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship

ELİF ÖZSU, Semra Cetinkaya, Semih Bolu, NİHAL HATİPOĞLU, Senay Savas Erdeve, SAADET OLCAY EVLİYAOĞLU, Firdevs BAŞ, Atilla Çayır, İSMAİL DÜNDAR, Emine Demet Akbas, Seyid Ahmet Ucakturk, Merih Berberoglu ve 13 yazar daha

• WoS Q3
• Scopus Q2
• WoS 17 atıf

17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort

ZEYNEP ŞIKLAR, EMİNE ÇAMTOSUN, Semih Bolu, Melek Yildiz, AYŞEHAN AKINCI, Firdevs Bas, İSMAİL DÜNDAR, Asli Bestas, Edip Unal, Pinar Kocaay, TÜLAY GÜRAN, Gonul Buyukyilmaz ve 28 yazar daha

• WoS Q3
• Scopus Q2
• WoS 13 atıf
• PlumX

Assessment of Executive Function Skills in Children with Isolated Growth Hormone Deficiency: A Cross-sectional Study

Guelsum Yitik Tonkaz, Atilla Çayır

• WoS Q3
• Scopus Q2
• WoS 1 atıf

Severe Early-Onset Obesity and Diabetic Ketoacidosis due to a Novel Homozygous c.169C>T p.Arg57*Variant in CEP19 Gene

Atilla Çayır, AYBERK TÜRKYILMAZ, Hannah Rabenstein, Fadime Güven, Yuksel Sumeyra Karagoz, Dogus Vuralli, Martin Wabitsch, HÜSEYİN DEMİRBİLEK

• WoS Q4
• Scopus Q4
• WoS 1 atıf

Levotiroksin Zehirlenmesi Olan Çocukların Klinik Özellikleri

DENİZ ÖKDEMİR, Atilla Çayır, FATİH GÜRBÜZ, ERDAL KURNAZ, HÜSEYİN DEMİRBİLEK, AYŞE SENA DÖNMEZ

Severe early-onset obesity and diabetic ketoacidosis due to a novel homozygous c.169C > T p.Arg57*mutation in CEP19 gene

Atilla Çayır, Ayberk Turkyilmaz, Hannah Rabenstein, Fadime Güven, Yuksel Sumeyra Karagoz, Martin Wabitsch, HÜSEYİN DEMİRBİLEK

• WoS Q2
• Scopus Q1

Evaluation of Seroprevalences of Vaccine Preventable Diseases in Children Admitted to a Regional Training and Research Hospital

ASUMAN NUR KARHAN, Atilla Çayır, SONER SERTAN KARA

Could Fetuin-A Be a Biomarker for Autism Spectrum Disorder and Cognitive Developmental Delay?

Nezahat Kurt, Fatma Betül Özgeriş, İlknur Ucuz, Zafer Bayraktutan, Kubra Kocak Yilmaz, Esen Yıldırım Demirdöğen, Atilla Çayır

• WoS Q3
• Scopus Q2
• WoS 2 atıf
• PlumX

High Fetuin-A Levels in Children with Celiac Disease

NEZAHAT KURT, Fatma Betül Özgeriş, Burcu Volkan, Mehmet Ali Gul, Atilla Çayır

• Scopus Q2
• PlumX

Relationship between the TAS2R38 and TAS1R2 polymorphisms and the dental status in obese children

Münevver KILIÇ, Taşkın GÜRBÜZ, Çiğdem Yüce Kahraman, Atilla Çayır, Abdulbaki BİLGİÇ, YUSUF KURT

• Scopus Q2
• WoS 8 atıf

Alterations of Neuroretinal and Corneal Thickness in Hashimoto’s Thyroiditis

OSMAN OKAN OLCAYSÜ, BUĞRA KARASU, ELİF OLCAYSÜ, Atilla Çayır, ALİ RIZA CENK ÇELEBİ

Is Serum Progranulin Level a Biomarker in Autism and Cognitive Development Disorders?

Fatma Betül Özgeriş, NEZAHAT KURT, İLKNUR UCUZ, KÜBRA KOÇAK YILMAZ, MEVLÜT SAİT KELEŞ, Atilla Çayır, ONUR BURAK DURSUN

• Scopus Q2
• WoS 3 atıf
• PlumX

EVALUATION OF THE RELATIONSHIPS BETWEEN OBESITY AND CENTRAL RETINAL THICKNESS, RETINAL NERVE FIBER LAYER, INTRAOCULAR PRESSURE, AND CENTRAL CORNEAL THICKNESS IN CHILDREN

OSMAN OKAN OLCAYSÜ, BUĞRA KARASU, ELİF OLCAYSÜ, Atilla Çayır, ALİ RIZA CENK ÇELEBİ

The Relationship between Psychopathology, Self-esteem, Body Perception and Serum Sex Steroids in Pubertal Gynecomastia

Semiha Comertoglu Arslan, İbrahim Selçuk Esin, Atilla Çayır, Zerrin Orbak, Onur Burak Dursun

• WoS Q2
• Scopus Q2
• WoS 11 atıf
• PlumX

Can Uric Acid Be A Marker For Metabolically Unhealthy Obesity in Children and Adolescents?

ERDAL KURNAZ, AYBERK TÜRKYILMAZ, Atilla Çayır

Screening of MC4R, LEP, LEPR, POMC, SH2B1, and SIM1 genes in Turkish children with severe early-onset obesity

AYBERK TÜRKYILMAZ, OĞUZHAN YARALI, ERDAL KURNAZ, Atilla Çayır

Toll-like receptor polymorphism associated with neonatal sepsis in term babies.

Soner Sertan Kara, Hasan Kahveci, Hasan Doğan, Fuat Laloğlu, Atilla Çayır

İnfantil hemanjiomların tedavisinde topikal beta-blokerlerin etkinliği

GÖKÇE PINAR REİS, ALİ PARLAKYİĞİT, Atilla Çayır, ALİ FETTAH, BURCU VOLKAN

Effects of chronotype and sleep duration on life quality and psychopathology in childhood obesity.

Ibrahim S Esin, Onur B Dursun, Esen Demirdogen, Esra O Asıkhasanoglu, Semiha C Aslan, Kezban Ozturk, Atilla Çayır

• Scopus Q3

Comparison of Treatment Regimens in Management of Severe Hypercalcemia Due to Vitamin D Intoxication in Children

Korcan Demir, Hakan Döneray, Cengiz Kara, Zeynep Atay, Semra Cetinkaya, Atilla Çayır, Ahmet Anık, Erdal Eren, Ahmet Ucakturk, Gulay Can Yilmaz, Ayca Torel Ergur, Mustafa Kendirci ve 5 yazar daha

• WoS Q2
• Scopus Q2
• WoS 15 atıf
• PlumX

Comparison of Treatment Regimens for the Management of Severe Hypercalcemia due to Vitamin D Intoxication in Children

KORCAN DEMİR, Hakan Döneray, CENGİZ KARA, ZEYNEP ATAY, SEMRA ÇETİNKAYA, Atilla Çayır, AHMET ANIK, ERDAL EREN, AHMET UÇAKTÜRK, GÜLAY CAN YILMAZ, AYÇA TÖREL ERGÜR, MUSTAFA KENDİRCİ ve 5 yazar daha

• WoS Q3
• Scopus Q2
• PlumX

Evaluation of Hearing in Children with Metabolic Syndrome

Korhan Kılıç, Muhammed Sedat Sakat, Atilla Çayır

• WoS 5 atıf
• PlumX

Bone mineral density and vitamin K status in children with celiac disease: Is there a relation?

Burcu VOLKAN, Ali FETTAH, Ali İŞLEK, Soner Sertan KARA, Nezahat Kurt, Atilla Çayır

• WoS Q4
• Scopus Q3
• WoS 15 atıf

Hearing Evaluation in Children with Type 1 Diabetes Mellitus

Muhammed Sedat Sakat, Korhan Kılıç, Atilla Çayır

• Scopus Q2
• PlumX

Endothelial dysfunction biomarker, endothelial cell-specific molecule-1, and pediatric metabolic syndrome

Iclal HALICI, Saziye Sezin Palabiyik, Fatma Güdücü Tüfekci, Asli OZBEK-BILGIN, Atilla Çayır

• WoS Q4
• Scopus Q3
• WoS 8 atıf

The Place of Atopy in the Aetiology of Acute Appendicitis in Children

M. N. Cevizci, A SÖĞÜT, Atilla Çayır, M DEMİR, Sevilay Özmen, F ERDOĞAN

• WoS Q4
• Scopus Q1
• WoS 4 atıf

Vici Syndrome in Siblings Born to Consanguineous Parents

Sener Tasdemir, Ibrahim Sahin, Atilla Çayır, Ihsan Yuce, Serdar CEYLANER, Abdulgani Tatar

• WoS Q3
• Scopus Q3
• WoS 14 atıf

A BIOMARKER FOR AUTISTIC SPEKTRUM DISORDER FETUIN A

Nezahat KURT, Fatma Betül Özgeriş, İlknur İbili UCUZ, Atilla Çayır, Nuri BAKAN

• WoS Q4
• Scopus Q4

Plasma Kisspeptin Levels in Newborn Infants with Breast Enlargement

Avni Kaya, Zerrin Orbak, Harun Polat, Atilla Çayır, Abdullah Erdil, Hakan Döneray

• WoS Q2
• Scopus Q2
• WoS 8 atıf
• PlumX

ÇOCUK DİŞ HEKİMLİĞİNDE OBEZİTE

MÜNEVVER ÇORUH, TAŞKIN GÜRBÜZ, Atilla Çayır

Clinical Profile of Familial Mediterranean Fever in a Paediatric Population in Eastern Turkey.

Celalettin Kosan, N DIRI, Atilla Çayır, MI TURAN

• WoS Q4
• Scopus Q3
• WoS 5 atıf

The effect of lifestyle change and metformin therapy on serum arylesterase and paraoxonase activity in obese children

Atilla Çayır, Mehmet Ibrahim Turan, FATİH GÜRBÜZ, Nezahat KURT, Abdulkadir YILDIRIM

• WoS Q4
• Scopus Q2
• WoS 7 atıf

Growth Hormone Therapy in Children with Chronic Renal Failure

Atilla Çayır, Celalettin KOŞAN

• Scopus Q3
• WoS 3 atıf

Food allergy knowledge and attitude of restaurant personnel in Turkey

Ayhan Sogut, Ayse Baccioglu Kavut, Ibrahim Kartal, Ercument Nazim Beyhun, Atilla Çayır, Mehmet Mutlu, Behzat Ozkan

• WoS Q1
• Scopus Q1
• WoS 22 atıf

The phenotypic and molecular genetic spectrum of Alstrom syndrome in 44 Turkish kindreds and a literature review of Alstrom syndrome in Turkey

Aysegul Ozanturk, Jan D. Marshall, Gayle B. Collin, SELMA DÜZENLİ, Robert P. Marshall, Sukru Candan, Tulay Tos, Ihsan Esen, MUSTAFA TAŞKESEN, Atilla Çayır, Sukru Ozturk, Ihsan Ustun ve 16 yazar daha

• WoS Q3
• Scopus Q2
• WoS 42 atıf

RECURRENT RAB3GAP1 MUTATIONS IN THE TURKISH POPULATION

Şener TAŞDEMİR, I. Sahini, D. J. Morris-Rosendahl, EBRU MARZİOĞLU, Atilla Çayır, İhsan YÜCE, Abdulgani Tatar

• WoS Q4
• Scopus Q4
• WoS 5 atıf

SERUM LEVELS OF PROGRANULIN IN CHILDREN WITH COGNITIVE DEVELOPMENTAL DELAY AND AUTISM SPECTRUM DISORDER

Fatma Betül Özgeriş, Nezahat KURT, İLKNUR İBİLİ UCUZ, KÜBRA KOÇAK YILMAZ, Mevlüt Sait KELEŞ, Atilla Çayır, Onur Burak DURSUN

• WoS Q4
• Scopus Q4

Antioxidant Status in Blood of Obese Children: The Relation between Trace Elements, Paraoxonase, and Arylesterase Values

Yasemin Çayır, Atilla Çayır, Mehmet Ibrahim Turan, Nezahat Kurt, Mustafa Kara, Esra Laloğlu, Murat CİFTEL, Abdulkadir Yildirim

• WoS Q4
• Scopus Q2
• WoS 25 atıf
• PlumX

Clinical characteristics of patients presented with primary adrenal insufficiency due to a p. R451W mutation in the CYP11A1 gene

Atilla Çayır, HÜSEYİN DEMİRBİLEK, MEHMET NURİ ÖZBEK, İlknur Kurt, MURAT KARAOĞLAN, SERPİL ALBAYRAK, BUMİN NURİ DÜNDAR, TÜLAY GÜRAN

Psychogenic Polydipsia Complicated With Seizures in a 13 Year Old Child: A Case Report

Ö Yendur, Atilla Çayır, ZÜHAL GÜNDOĞDU

Steroid 11β-hidroksilaz eksikliği olan 100 çocuk hastanın klinik bulgularının genetik ve adrenokortikal hormonprofili ile ilişkisinin değerlendirilmesi

MELEK YILDIZ, EMREGÜL IŞIK, SERAP DEMİRCİOĞLU, MEHMET KESKİN, MEHMET NURİ ÖZBEK, FİRDEVS BAŞ, AHMET SEYİT UÇAKTÜRK, MUAMMER BÜYÜKİNAN, CENGİZ KARA, LISE BERNARD, HASAN ÖNAL, FATMA FEYZA DARENDELİLER ve 13 yazar daha

Turner Sendromu benzeri klinik bulgularla prezente olan 18p delesyon sendromu: Bir olgu sunumu

AYŞE ÖZDEN, Atilla Çayır, AYBERK TÜRKYILMAZ

Tip 1 Diyabetes Mellituslu Çocuk ve Ergenlerde HbA1c Ölçüm Yöntemlerinin Karşılaştırılması

ERDAL KURNAZ, MAHMUT ŞENYURT, KONCA ALTINKAYNAK, Atilla Çayır

Türkiyede Çocukluk Çağı Adrenokortikal Karsinomalarda TP53 Mutasyonu Taraması: Çok merkezli çalışma

ENVER ŞİMŞEK, OĞUZ ÇİLİNGİR, ÇİĞDEM BİNAY, MELİHA DEMİRAL, KÖNÜL HAZIYEVA, SEVİLHAN ARTAN, METİN YILDIZ, SEMRA ÇETİNKAYA, OYA ERCAN, Atilla Çayır, ELİF SÖBÜ, ONUR AKIN ve 4 yazar daha

Çok Merkezli Olarak Hipofosfatemik Riketsli Olguların Değerlendirilmesi

ZEYNEP ŞIKLAR, Serap Turan, ABDULLAH BEREKET, AYHAN ABACI, TÜLAY GÜRAN, KORCAN DEMİR, Azad Akberzade, FİRDEVS BAŞ, ECE BÖBER, Mehmet Nuri Ozbek, CENGİZ KARA, ŞÜKRAN POYRAZOĞLU ve 24 yazar daha

Metabolik Sendrom Çocuklarda İşitmeyi Etkiler mi?

Korhan Kılıç, Muhammed Sedat Sakat, Atilla Çayır

Metabolik Sendromlu Çocuklarda İşitmenin Değerlendirilmesi

Korhan Kılıç, Muhammed Sedat Sakat, Atilla Çayır

Is Gynecomastia An Endocrinological Disorder Or A Psychoendocrinological Disorder?

SEMİHA ARSLAN, ONUR BURAK DURSUN, İBRAHİM SELÇUK ESİN, Atilla Çayır, Zerrin Orbak

Çocuklarda Beslenme ve Besin Kaynakları

Yusuf Kenan Haspolat, Hakan Döneray, Serkan Atıcı, Atilla Çayır

Gecikmiş Ergenlik

Atilla Çayır

D Vitamini Bağımlı Rikets

ÖZGE KÖPRÜLÜ, Atilla Çayır

İdrar Yolu Enfeksiyonu

Ayşe Sena Dönmez, Atilla Çayır

Rotavirüs Enfeksiyonu

Esra Dişçi, Atilla Çayır

GENERAL APPROACH OF DISORDERS OF SEX DIFFERENTIATION

Esra Dişçi, Atilla Çayır

Cinsiyet Gelişim Bozuklukları

Atilla Çayır

Kalsiyopenik Raşitizmin Genetik Formları

Atilla Çayır, ERDAL KURNAZ

ADRENAL INSUFFICIENCY IN CHILDREN AND ADOLESCENTS

Gözde Doymuş, Atilla Çayır

NÖROKUTAN HASTALIKLARIN ENDOKRIN BULGULARI VE YÖNETIMI

Atilla Çayır, Ömer Uysal

ÇOCUKLARDA OBEZİTE VE TOPLUM

KENAN ÇETİN, Atilla Çayır