Merih Berberoglu
0000-0003-3102-0242
155 papers found
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Diagnostic Value of Contrast-Enhanced MR Angiography in a Child With MIBG-Negative Recurrent Pheochromocytoma:
Evaluation of Glucose Homeostasis in Transfusion-Dependent Thalassemic Patients
The effect of growth hormone treatment on bone mineral density in prepubertal girls with Turner syndrome: a multicentre prospective clinical trial
Hypocalcemic seizure due to congenital rickets in the first day of life
Factors Contributing to Sex Assignment and Reassignment Decisions in Turkish Children with 46,XY Disorders of Sex Development
Biopsychosocial variables associated with gender of rearing in children with male pseudohermaphroditism
Evaluation of insulin resistance in Turkish girls with premature pubarche using the homeostasis assessment (HOMA) model
Functional Ovarian Hyperandrogenism and Polycystic Ovary Syndrome in Prepubertal Girls with Obesity and/or Premature Pubarche
Disorders of gonadal development: A broad clinical, cytogenetic and histopathologic spectrum
The Incidence and Evolution of Thyroid Dysfunction During Interferon-α Therapy in Children with Chronic Hepatitis Β Infection
Growth hormone analysis and treatment in Ellis–van Creveld syndrome
Effects of Growth Hormone on Growth, Insulin Resistance and Related Hormones (Ghrelin, Leptin and Adiponectin) in Turner Syndrome
Testicular adrenal rests in a patient with congenital adrenal hyperplasia: US and MRI features
5α steroid reductase deficiency in Turkey
Isolated Central Diabetes Insipidus in a Newborn with Congenital Toxoplasmosis
Plasminogen activator inhibitor-1 (PAI-1) gene polymorphism (-675 4G/5G) associated with obesity and vascular in risk in children
Experience with Long-term Glucocorticoid Treatment in Congenital Adrenal Hyperplasia: Growth Pattern Compared with Genetic Height Potential
Incidence of Iodine Deficiency in Patients Presenting with Goitre - Discrepancy Between Clinical and Ultrasonographic Evaluation of the Thyroid: Comparison of Patients With and Without Autoimmune Thyroiditis - Clinical, Hormonal and Urinary Iodine Excretion Studies
Severe Growth Hormone Insensitivity Resulting from Total Absence of Signal Transducer and Activator of Transcription 5b
Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained byTPITGene Mutations
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