Tarik Kirkgoz
Ihlas Marmara Evleri - I. Kisim, Turkey
Last Updated: 09/26/2026
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Found 15 publications
Adrenal androgens as predictors of growth characteristics in premature pubarche.
Journal: European journal of endocrinology
Published: December 09, 2025
Clinical and molecular characterization of 5α-reductase deficiency type 2: First report of a family with homozygous deletion in exon 1 of SRD5A2.
Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
Published: April 30, 2025
Body composition assessment measured via bioelectrical impedance analysis in euthyroid children with newly diagnosed Hashimoto's thyroiditis.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: August 28, 2024
Clinical and Molecular Genetic Characteristics of Patients with Hereditary Hypophosphatemia.
Journal: The Journal of clinical endocrinology and metabolism
Published: August 08, 2024
Genetic diagnosis of congenital hypopituitarism in Turkish patients by a target gene panel: novel pathogenic variants in GHRHR, GLI2, LHX4 and POU1F1 genes.
Journal: Archives of endocrinology and metabolism
Published: November 10, 2023
Challenges in the Management of a 7-Year-Old Child with Thyrotropin-Secreting Pituitary Adenoma and the Review of the Literature.
Journal: Hormone research in paediatrics
Published: August 19, 2022
Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features.
Journal: Calcified tissue international
Published: August 18, 2021
Does Genotype-Phenotype Correlation Exist in Vitamin D-Dependent Rickets Type IA: Report of 13 New Cases and Review of the Literature.
Journal: Calcified tissue international
Published: September 18, 2020
Cinacalcet as a First-Line Treatment in Neonatal Severe Hyperparathyroidism Secondary to Calcium Sensing Receptor (CaSR) Mutation.
Journal: Hormone research in paediatrics
Published: June 20, 2020
A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age.
Journal: Calcified tissue international
Published: November 20, 2019
Persistent Müllerian Duct Syndrome: A Rare But Important Etiology of Inguinal Hernia and Cryptorchidism.
Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation
Published: September 30, 2019
Management of Systemic Hypersensitivity Reactions to Gonadotropin-Releasing Hormone Analogues during Treatment of Central Precocious Puberty.
Journal: Hormone research in paediatrics
Published: August 07, 2019
Last Updated: 09/26/2026