Ahmet R. Arman

Istanbul, Turkey

Last Updated: 09/26/2026

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Found 32 publications

Growth Hormone Strongly Induces hSMN2 Promoter Driving Construct Gene Expression in Mammalian Cells

Growth Hormone Strongly Induces hSMN2 Promoter Driving Construct Gene Expression in Mammalian Cells

Journal: Journal of clinical research in pediatric endocrinology

Published: August 28, 2025

Decoding the Genetic Puzzle of Inherited Retinal Dystrophies: Novel Insights From a Turkish Cohort.

Decoding the Genetic Puzzle of Inherited Retinal Dystrophies: Novel Insights From a Turkish Cohort.

Journal: Clinical genetics

Published: February 20, 2025

Expanding the Clinical Features of Schimke Immuno-osseous Dysplasia: a New Patient with a Novel Variant and Novel Clinical Findings

Expanding the Clinical Features of Schimke Immuno-osseous Dysplasia: a New Patient with a Novel Variant and Novel Clinical Findings

Journal: Journal of clinical research in pediatric endocrinology

Published: August 08, 2024

Clinical and Molecular Genetic Characteristics of Patients with Hereditary Hypophosphatemia.

Clinical and Molecular Genetic Characteristics of Patients with Hereditary Hypophosphatemia.

Journal: The Journal of clinical endocrinology and metabolism

Published: August 08, 2024

Identification of Novel Variants in the NHS in Four Turkish Patients With Nance-Horan Syndrome.

Identification of Novel Variants in the NHS in Four Turkish Patients With Nance-Horan Syndrome.

Journal: American journal of medical genetics. Part A

Published: May 08, 2024

The effect of growth hormone on motor findings and dendrite morphology in an experimental Parkinson's disease model.

The effect of growth hormone on motor findings and dendrite morphology in an experimental Parkinson's disease model.

Journal: Anatomical science international

Published: November 02, 2023

Vitamin D Receptor Polymorphisms Among the Turkish Population are Associated with Multiple Sclerosis.

Vitamin D Receptor Polymorphisms Among the Turkish Population are Associated with Multiple Sclerosis.

Journal: Balkan journal of medical genetics : BJMG

Published: March 07, 2023

Novel, homozygous RAB3GAP1 c.2606 + 1G>A, p.Glu830ValfsTer9 variant and chromosome 3q29 duplication in a Turkish individual with Warburg micro syndrome.

Novel, homozygous RAB3GAP1 c.2606 + 1G>A, p.Glu830ValfsTer9 variant and chromosome 3q29 duplication in a Turkish individual with Warburg micro syndrome.

Journal: Clinical dysmorphology

Published: March 06, 2023

Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central precocious puberty.

Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central precocious puberty.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: December 29, 2022

Array-Based Comparative Genomic Hybridization Analysis in Children with Developmental Delay/Intellectual Disability.

Array-Based Comparative Genomic Hybridization Analysis in Children with Developmental Delay/Intellectual Disability.

Journal: Balkan journal of medical genetics : BJMG

Published: October 17, 2022

Two new cases with novel pathogenic variants reflecting the clinical diversity of Schaaf-Yang syndrome.

Two new cases with novel pathogenic variants reflecting the clinical diversity of Schaaf-Yang syndrome.

Journal: Clinical genetics

Published: July 17, 2022

Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity.

Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity.

Journal: JBMR plus

Published: April 29, 2022

Showing 1-12 of 32

Last Updated: 09/26/2026