journal of clinical research in pediatric endocrinology سال:2015 - دوره:7

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journal of clinical research in pediatric endocrinology
سال:2015 - دوره:7 - شماره:Suppl 1

A novel GH1 functional mutation in a family with isolated growth hormone deficiency - صفحه:13- A rare case of neonatal diabetes due to COQ2 gene mutation - صفحه:16- ABCC8 frameshift mutation in exon 28 (C.3512delT) is a founder mutation for autosomal recessive hyperinsulinemic hypoglycemia in Eastern Anatolia - صفحه:20- Aromatase inhibitors in paediatric endocrinology - صفحه:6- Dear colleagues and guests - صفحه:1- Editorial Follow-up of two cases of medulloblastoma with/without growth hormone therapy - صفحه:17-18 Genetics and clinical characteristics of neonatal diabetes - صفحه:7- Growth hormone therapy in five patients with malignant intracranial tumors - صفحه:9- Growth hormone treatment in childhood intracranial tumors - hacettepe experience - صفحه:8- Growth without growth hormone syndrome in a patient with craniopharyngioma - صفحه:19- HADH mutation is a rare cause of hyperinsulinaemic hypoglycaemia - صفحه:12- Idiopathic short stature - صفحه:2- Insulin-like growth factor treatment of growth disorders - صفحه:3- Linical and molecular characterisation of patients with congenital hyperinsulinism - صفحه:5- Long-term endocrine evaluation of childhood brain tumors - صفحه:22- Management of growth hormone deficiency in children irradiated for brain tumours - صفحه:4- Mutant neurogenin-3 in permanent neonatal diabetes and congenital malabsorptive diarrhea - صفحه:10- Persistent hyperinsulinemic hypoglycemia due to SUR1 (ABCC8) mutation in newborn twins: An eight-year follow-up - صفحه:14- Premature menarche associated with mccune-albright syndrome in an infant - صفحه:11- Primary melanocytic suprasellar tumor presenting with growth hormone deficiency - صفحه:15- The evolution of body size Treatment of growth hormone deficiency in langerhans cell histiocytosis - صفحه:21-