Dergiler / Journal of Clinical Research in Pediatric Endocrinology
2021 · Cilt: 13 - Sayı: 3
| Makale | Yazar | Sayfa |
|---|---|---|
| Traditional and New Methods of Bone Age Assessment-An Overview | Monika PROKOP PIOTRKOWSKA,Kamila MARSZALEK DZIUBA,El bieta MOSZCZYNSKA,Mieczys aw SZALECKI,El bieta JURKIEWICZ | 251–262 |
| Pre-treatment Neutropenia in Children and Adolescents with Autoimmune Hyperthyroidism | Melissa Kaori S. LITAO,Ana Gutierrez ALVAREZ,Bina SHAH | 263–268 |
| Basal Serum Thyroxine Level should Guide Initial Thyroxine Replacement Dose in Neonates with Congenital Hypothyroidism | Ceren GÜNBEY,Alev OZON,Nazlı GÖNÇ,Ayfer ALİKAŞİFOĞLU,Sevilay KARAHAN,Nurgün KANDEMİR | 269–275 |
| Evaluation of Children and Adolescents with Thyroid Nodules: A Single Center Experience | Selin ELMAOĞULLARI,Şervan ÖZALKAK,Semra ÇETİNKAYA,İBRAHİM KARAMAN,Çiğdem ÜNER,Nilüfer ARDA,Şenay ERDEVE,Zehra AYCAN | 276–284 |
| An Evaluation of Glucagon Injection Anxiety and Its Association with the Fear of Hypoglycemia among the Parents of Children with Type 1 Diabetes | Serra MURADOĞLU,Gül YEŞİLTEPE MUTLU,Tuğba GÖKÇE,Ecem CAN,Şükrü HATUN | 285–292 |
| Midkine: Utility as a Predictor of Early Diabetic Nephropathy in Children with Type 1 Diabetes Mellitus | Kotb Abbass METWALLEY,Hekma Saad FARGHALY,Magda Farghali GABRI,Safwat Mohamed ABDEL AZIZ,Asmaa Mohamed ISMAIL,Duaa MOHAMED RAFAAT,Islam Fathy ELNAKEEB | 293–299 |
| Long-term Clinical Follow-up of Patients with Familial Hypomagnesemia with Secondary Hypocalcemia | Elvan BAYRAMOĞLU,Meliksah KESKİN,Zehra AYCAN,Şenay ERDEVE,Semra ÇETİNKAYA | 300–307 |
| Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome | Aydilek DAĞDEVİREN ÇAKIR,Firdevs BAŞ,Onur AKIN,Zeynep ŞIKLAR,Bahar ÖZCABI,Merih BERBEROĞLU,Aslı Derya KARDELEN,Elvan BAYRAMOĞLU,Şükran POYRAZOĞLU,Murat AYDIN,Ayça ERGÜR,Damla GÖKŞEN,Semih BOLU,Zehra AYCAN,Beyhan TÜYSÜZ,OYA ERCAN,Olcay EVLİYAOĞLU | 308–319 |
| The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region | SİNEM YALÇINTEPE,Fatma Özgüç ÇÖMLEK,Hakan GÜRKAN,Selma DEMİR,Emine İkbal ATLI,ENGİN ATLI,Damla EKER,Filiz TÜTÜNCÜLER | 320–331 |
| Evaluation of Growth Hormone Results in Different Diagnosis and Trend Over 10 Year of Follow-up: A Single Center Experience | Zehra AYCAN,Aslıhan ARASLI YILMAZ,Servet YEL,Şenay ERDEVE,Semra ÇETİNKAYA | 332–341 |
| Vandetanib in a Child Affected by Neurofibromatosis Type 1 and Medullary Thyroid Carcinoma with Both NF1 and Homozygous RET Proto-oncogen Germ-line Mutations | Begümhan DEMİR GÜNDOĞAN,Fatih SAĞCAN,Sevcan Tuğ BOZDOĞAN,YÜKSEL BALCI,Ferah TUNCEL,Elvan Çaglar ÇITAK | 342–346 |
| Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin | Carla BIZZARRI,Germana Antonella GIANNONE,Jacopo GERVASONI,Sabina BENEDETTI,Federica ALBANESE,Luca Dello STROLOGO,Isabella GUZZO,Mafalda MUCCIOLO,Francesca Diomedi CAMASSEI,Francesco EMMA,Marco CAPPA,Ottavia PORZIO | 347–352 |
| A Case of Congenital Central Hypothyroidism Caused by a Novel Variant (Gln1255Ter) in IGSF1 Gene | Doğa TÜRKKAHRAMAN,Nimet KARATAŞ TORUN,Nadide Cemre RANDA | 353–357 |
| Brain Abscess in a Patient with Osteopetrosis: A Rare Complication | Merve İŞERİ NEPESOV,Eylem KIRAL,Gürkan BOZAN,Ömer KILIÇ,Kürşat Bora CARMAN,Çoşkun YARAR,Suzan SAYLISOY,Ener Çağrı DİNLEYİCİ | 358–361 |
| Co-existence of Congenital Adrenal Hyperplasia and Familial Hypokalemic Periodic Paralysis due to CYP21A2 and SCN4A Pathogenic Variants | Tuğba ÇETİN,İhsan TURAN | 362–366 |
| Analysis of the Performance of Neck Circumference to Identify Overweight and Obese Children | Manuel Andr VIRU LOZA | 367–368 |
| In reply Asif M et al. | Muhammad ASIF,Muhammad ASLAM | 369–369 |