Dergiler / Journal of Clinical Research in Pediatric Endocrinology
Journal of Clinical Research in Pediatric EndocrinologyFen
2022 · Cilt: 14 - Sayı: 1
| Makale | Yazar | Sayfa |
|---|---|---|
| Recommendations for Clinical Decision-making in Children with Type 1 Diabetes and Celiac Disease: Type 1 Diabetes and Celiac Disease Joint Working Group Report | Şükrü 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,Mukadde | 1–9 |
| 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 Patients | Sare Betül KAYGUSUZ, Tülay GÜRAN, Serap TURAN, Abdullah BEREKET, Mehmet ELTAN, Tarık KIRKGÖZ, Zehra Yavaş ABALI, Didem HELVACIOĞLU, Tuba Seven MENEVŞE, Büşra Gürpınar TOSUN | 10–16 |
| Feminizing Adrenocortical Tumors as a Rare Etiology of Isosexual/Contrasexual Pseudopuberty | Doğuş VURALLI,Nazlı GÖNÇ,Alev OZON,Saniye EKİNCİ,Hasan Serkan DOĞAN,Serdar TEKGÜL,Ayfer ALİKAŞİFOĞLU | 17–28 |
| Diagnostic Value of Bilateral Petrosal Sinus Sampling in Children with Cushing Disease: A Multi-center Study | Eren ER, Gönül ÇATLI, Oya ERCAN, Ayşehan AKINCI, Bumin DÜNDAR, Saadet Olcay EVLİYAOĞLU, Aslı Derya KARDELEN, Ece BÖBER, Hande TURAN, Özgecan DEMİRBAŞ, Semra ÇETİNKAYA | 29–36 |
| Mutation Screening and Functional Study of SLC26A4 in Chinese Patients with Congenital Hypothyroidism | Chang 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 SONG | 46–55 |
| Serum Neudesin Levels in Obese Adolescents | Çiğdem BİNAY, Aliye ÇELİKKOL, Savaş GÜZEL, Özge AYÇİÇEK | 69–75 |
| Genetic Indices Relationship to Hyperglycemia-associated Biomarkers: Consistency with miRNA Expression in Egyptian Children with T1DM | Naglaa Fathy BARSEEM, Marwa Mohamed MAHASAB, Ibrahem Fathy ZAED, Aya Eldesoky A. SAİD, Eman Masoud Abd El GAYED | 76–86 |
| Investigating Genetic Mutations in a Large Cohort of Iranian Patients with Congenital Hyperinsulinism | Rahim VAKİLİ, Maryam Razzaghy AZAR, Saeedeh SAEEDİ, Sepideh Borhan DAYANİ, Samaneh ENAYATİ, Somayyeh HASHEMİAN, Peyman ESHRAHGİ, Siroos KARİMDADİ, Parisa TAJDİNİ, Farzaneh ABBASİ |