Dergiler / Journal of Clinical Research in Pediatric Endocrinology

2022 · Cilt: 14 - Sayı: 1

MakaleYazarSayfa
Recommendations for Clinical Decision-making in Children with Type 1 Diabetes and Celiac Disease: Type 1 Diabetes and Celiac Disease Joint Working Group ReportŞükrü HATUN,Buket DALGIÇ,Damla GÖKŞEN,Sema AYDOĞDU,Şenay ERDEVE,Zarife KULOĞLU,Yaşar DOĞAN,Zehra AYCAN,Gül Yeşiltepe MUTLU,Nuray Uslu KIZILKAN,Alev KESER,Ömer Faruk BEŞER,Mehmet Nuri ÖZBEK,Aysun BİDECİ,Deniz ERTEM,Olcay EVLİYAOĞLU,Beyza TİPİCİ,TUĞBA GÜRSOY KOCA,Firdevs BAŞ,Feyza DARENDELİLER,Mukadde1–9
Efficacy of the Novel Degludec/Aspart Insulin Co-formulation in Children and Adolescents with Type 1 Diabetes: A Real-life Experience with One Year of IDegAsp Therapy in Poorly Controlled and Non-compliant PatientsSare Betül KAYGUSUZ, Tülay GÜRAN, Serap TURAN, Abdullah BEREKET, Mehmet ELTAN, Tarık KIRKGÖZ, Zehra Yavaş ABALI, Didem HELVACIOĞLU, Tuba Seven MENEVŞE, Büşra Gürpınar TOSUN10–16
Feminizing Adrenocortical Tumors as a Rare Etiology of Isosexual/Contrasexual PseudopubertyDoğuş VURALLI,Nazlı GÖNÇ,Alev OZON,Saniye EKİNCİ,Hasan Serkan DOĞAN,Serdar TEKGÜL,Ayfer ALİKAŞİFOĞLU17–28
Diagnostic Value of Bilateral Petrosal Sinus Sampling in Children with Cushing Disease: A Multi-center StudyEren ER, Gönül ÇATLI, Oya ERCAN, Ayşehan AKINCI, Bumin DÜNDAR, Saadet Olcay EVLİYAOĞLU, Aslı Derya KARDELEN, Ece BÖBER, Hande TURAN, Özgecan DEMİRBAŞ, Semra ÇETİNKAYA29–36
Mutation Screening and Functional Study of SLC26A4 in Chinese Patients with Congenital HypothyroidismChang Run ZHANG, Yuan Ping SHİ, Cao Xu ZHANG, Feng SUN, Wen Jiao ZHU, Ya FANG, Qian Yue ZHANG, Chen Yan YAN, Ying Xia YİNG, Shuang Xia ZHAO, Huai Dong SONG46–55
Serum Neudesin Levels in Obese AdolescentsÇiğdem BİNAY, Aliye ÇELİKKOL, Savaş GÜZEL, Özge AYÇİÇEK69–75
Genetic Indices Relationship to Hyperglycemia-associated Biomarkers: Consistency with miRNA Expression in Egyptian Children with T1DMNaglaa Fathy BARSEEM, Marwa Mohamed MAHASAB, Ibrahem Fathy ZAED, Aya Eldesoky A. SAİD, Eman Masoud Abd El GAYED76–86
Investigating Genetic Mutations in a Large Cohort of Iranian Patients with Congenital HyperinsulinismRahim VAKİLİ, Maryam Razzaghy AZAR, Saeedeh SAEEDİ, Sepideh Borhan DAYANİ, Samaneh ENAYATİ, Somayyeh HASHEMİAN, Peyman ESHRAHGİ, Siroos KARİMDADİ, Parisa TAJDİNİ, Farzaneh ABBASİ87–95
Comparison of Indonesian Growth Reference Chart and World Health Organization Child Growth Standard in Detecting Stunting: A Systematic Review and Meta-analysis of 15,874 ChildrenGilbert Sterling OCTAVİUS,Chelsea Serena br. PARDEDE,Cindy Clarissa THANDY,Clauvinna Adhityana Lie FISCA,Andry JULIANSEN96–101
Using Etomidate in a Two-month-old Infant with Cushing Syndrome due to Adrenocortical CarcinomaAhreum KWON, Yongha CHOİ, Jo Won JUNG, Junghwan SUH, Ho Seong KİM102–106
Precocious Pseudo-puberty in a Two-year-old Girl, Presenting with Bilateral Ovarian Enlargement and Progressing to Unilateral Juvenile Granulosa Cell TumourHager BARAKİZOU,Souha GANNOUNİ,Thouraya KAMOUN,Muhammed MEHDİ,Fernanda AMARY,Zilla HUMA,Anne Laure TODESCHİNİ,Reiner VEİTİA,Malcolm DONALDSON107–113
TSHRV656F Activating Variant of the Thyroid Stimulating Hormone Receptor Gene in Neonatal Onset Hyperthyroidism: A Case ReviewRıfat BİRCAN, Emine ÇAMTOSUN, Leman KAYAŞ, Ayşehan AKINCI114–118
Long-term Follow-up of a Toddler with Papillary Thyroid Carcinoma: A Case Report with a Literature Review of Patients Under 5 Years of AgeAyşe Pınar ÖZTÜRK,Esin ÖZTURHAN,Feryal Gun SOYSAL,Seher Nilgün ÜNAL,Emine Göknur IŞIK,Gülçin YEĞEN,SEMEN ÖNDER,Melek YILDIZ,Şükran POYRAZOĞLU,Firdevs BAŞ,Feyza DARENDELİLER119–125
Silent Corticotroph Tumor with Adrenocortical Choristoma in an Eleven-year-old BoyHande TURAN,Gürkan TARÇIN,Özgür METE,Ada Bulut SİNOPLU,Olcay EVLİYAOĞLU,Ayşim BÜGE ÖZ,OYA ERCAN126–130