Controversies in the diagnosis and management of growth hormone deficiency in childhood and adolescence | Archives of Disease in Childhood | 2016 | 83 |
Defining the Newborn Blood Spot Screening Reference Interval for TSH: Impact of Ethnicity | Journal of Clinical Endocrinology and Metabolism | 2016 | 25 |
Hepatocyte Nuclear Factor-4 Alfa Mutation Associated with Hyperinsulinaemic Hypoglycaemia and Atypical Renal Fanconi Syndrome: Expanding the Clinical Phenotype | Hormone Research in Paediatrics | 2016 | 21 |
Prediction of congenital hypothyroidism based on initial screening thyroid-stimulating-hormone | BMC Pediatrics | 2016 | 20 |
Management of Cushing syndrome in children and adolescents: experience of a single tertiary centre | European Journal of Pediatrics | 2016 | 19 |
Emerging treatments for severe obesity in children and adolescents | BMJ, The | 2016 | 18 |
Isolated Pancreatic Aplasia Due to a Hypomorphic PTF1A Mutation | Diabetes | 2016 | 16 |
Genotype and Phenotype Characteristics in 22 Patients with Vitamin D-Dependent Rickets Type I | Hormone Research in Paediatrics | 2016 | 14 |
Unusual Femur Stress Fractures in Children With Osteogenesis Imperfecta and Intramedullary Rods on Long-term Intravenous Pamidronate Therapy | Journal of Pediatric Orthopaedics | 2016 | 13 |
Bone histomorphometric changes in children with rheumatic disorders on chronic glucocorticoids | Pediatric Rheumatology | 2016 | 12 |
Severe Hyperinsulinaemic Hypoglycaemia in Beckwith-Wiedemann Syndrome due to Paternal Uniparental Disomy of 11p15.5 Managed with Sirolimus Therapy | Hormone Research in Paediatrics | 2016 | 8 |
Idiopathic postprandial hyperinsulinaemic hypoglycaemia | Journal of Pediatric Endocrinology and Metabolism | 2016 | 7 |
The urinary inflammatory profile in gluten free diet-adherent adolescents with type 1 diabetes and celiac disease | Journal of Diabetes and Its Complications | 2016 | 6 |
Fanconi Bickel Syndrome with Hypercalciuria due to GLUT 2 Mutation | Indian Pediatrics | 2016 | 2 |
Breastfeeding in the 21st century | Lancet, The | 2016 | 2 |
The Incidence and Clinical Features of Dual Thyroid Ectopia in Congenital Hypothyroidism | Journal of Clinical Endocrinology and Metabolism | 2016 | 2 |
Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and Hemihypertrophy | Hormone Research in Paediatrics | 2016 | 1 |
The adrenal gland: an evolution of the roles of genetic counsellors and medical geneticists in endocrine cancers | Diagnostic Histopathology | 2016 | 0 |