Ahmet Ucar

Halaskargazi Cad. Etfal St
Sisli, 34371, Turkey

Last Updated: 09/26/2026

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Found 55 publications

Microscopic Müllerian Duct Remnants in a 46,XY Individual with Genetically Confirmed 17α-Hydroxylase/17,20-Lyase Deficiency: an Unexpected Histopathological Finding.

Microscopic Müllerian Duct Remnants in a 46,XY Individual with Genetically Confirmed 17α-Hydroxylase/17,20-Lyase Deficiency: an Unexpected Histopathological Finding.

Journal: Journal of clinical research in pediatric endocrinology

Published: August 20, 2026

Revisiting the Association of Central Precocious Puberty with Neurovisceral Diseases owing to a Girl with Niemann-Pick Disease Type C.

Revisiting the Association of Central Precocious Puberty with Neurovisceral Diseases owing to a Girl with Niemann-Pick Disease Type C.

Journal: Journal of clinical research in pediatric endocrinology

Published: August 19, 2026

A Rare Cause of Thyroid Hormone Abnormalities in an Adolescent: A Case Report of SBP2 (SECISBP2) Deficiency.

A Rare Cause of Thyroid Hormone Abnormalities in an Adolescent: A Case Report of SBP2 (SECISBP2) Deficiency.

Journal: Molecular syndromology

Published: November 11, 2025

The first report of a gross deletion in the SCNN1G gene in a case presenting with hyponatremic convulsion at fifth year of treatment.

The first report of a gross deletion in the SCNN1G gene in a case presenting with hyponatremic convulsion at fifth year of treatment.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: July 01, 2025

Central precocious puberty in boys; diagnosis, treatment and follow-up: a nation-wide study.

Central precocious puberty in boys; diagnosis, treatment and follow-up: a nation-wide study.

Journal: Endocrine

Published: May 08, 2025

SGK3 promoter deletion in late-onset hypophosphatemic rickets, a possible genetic cause of the disease.

SGK3 promoter deletion in late-onset hypophosphatemic rickets, a possible genetic cause of the disease.

Journal: Orphanet journal of rare diseases

Published: March 05, 2025

Correction: Can fecal calprotectin be used as a biomarker of non-alcoholic fatty liver disease in obese adolescents?

Correction: Can fecal calprotectin be used as a biomarker of non-alcoholic fatty liver disease in obese adolescents?

Journal: BMC pediatrics

Published: January 08, 2025

Comparative Analysis of Girls With Slowly Progressive Central Precocious Puberty Vs. Rapidly Progressive Central Precocious Puberty: Single-Center Experience.

Comparative Analysis of Girls With Slowly Progressive Central Precocious Puberty Vs. Rapidly Progressive Central Precocious Puberty: Single-Center Experience.

Journal: Sisli Etfal Hastanesi tip bulteni

Published: December 30, 2024

Psychosocial Development, Sexuality and Quality of Life in Congenital Adrenal Hyperplasia

Psychosocial Development, Sexuality and Quality of Life in Congenital Adrenal Hyperplasia

Journal: Journal of clinical research in pediatric endocrinology

Published: December 23, 2024

17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort.

17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort.

Journal: Endocrine

Published: May 18, 2024

Successful Management of an Infant with Congenital Focal Hyperinsulinism with No Apparent Lesion During Surgery.

Successful Management of an Infant with Congenital Focal Hyperinsulinism with No Apparent Lesion During Surgery.

Journal: Sisli Etfal Hastanesi tip bulteni

Published: May 09, 2024

Comprehensive Insights Into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes from a Multicenter Study

Comprehensive Insights Into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes from a Multicenter Study

Journal: Journal of clinical research in pediatric endocrinology

Published: April 26, 2024

Showing 1-12 of 55

Last Updated: 09/26/2026