Merih Berberoglu
Ankara, Turkey
Last Updated: 09/26/2026
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Found 130 publications
An Unexpected Result in a Case of Gonadal Dysgenesis: Noonan Syndrome Caused by RIT1 Mutation.
Journal: Journal of clinical research in pediatric endocrinology
Published: June 16, 2026
Approach to The Patient With Combined Pituitary Hormone Deficiency Due to a Novel Homozygous LHX3 Variant.
Journal: Clinical endocrinology
Published: June 10, 2026
A rare, invasive, and challenging cancer in childhood: diffuse sclerosing variant of papillary thyroid carcinoma.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: April 18, 2026
Two threats in early life: congenital hyperinsulinemic hypoglycemia and thrombosis.
Journal: Therapeutic advances in endocrinology and metabolism
Published: January 07, 2026
Familial, constitutional, and combined idiopathic short stature: longitudinal growth patterns and pubertal effects.
Journal: Frontiers in pediatrics
Published: January 07, 2026
Turner syndrome across the lifespan: a 25-year single-center experience from neonatal diagnosis to adult outcomes.
Journal: Frontiers in endocrinology
Published: December 18, 2025
THE USE OF ORAL BISPHOSPHONATES IN REFRACTORY SEVERE HYPERCALCEMIA AFTER DENOSUMAB CESSATION.
Journal: Acta endocrinologica (Bucharest, Romania : 2005)
Published: October 10, 2025
Steroid profiling in congenital adrenal hyperplasia: comparing immunoassays and LC-MS/MS accuracy.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: September 21, 2025
The Impact of an Adolescent-Friendly Approach on Metabolic Control in Adolescents with Type 1 Diabetes in Türkiye.
Journal: Journal of clinical medicine
Published: September 04, 2025
Near-final height outcomes in children with idiopathic short stature responsive to the IGF-1 generation test: a multicenter retrospective study of rhGH therapy.
Journal: BMC endocrine disorders
Published: August 19, 2025
Pubertal characteristics, final height, and associated factors in patients with nonclassical congenital adrenal hyperplasia: a single center experience.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: August 14, 2025
Long-term Follow-up of a Case with TBX19 Mutation, a Rare Cause of Isolated ACTH Deficiency and Literature Review
Journal: Journal of clinical research in pediatric endocrinology
Published: July 29, 2025
Last Updated: 09/26/2026