Anatoly N. Tyulpakov
Moscow, MOW, Russian Federation
Last Updated: 09/26/2026
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Found 9 publications
Does everyone need to take vitamin D? High prevalence of CYP24A1 deficiency in the Russian population.
Journal: Problemy endokrinologii
Published: January 23, 2025
Diversity of Molecular Functions of RNA-Binding Ubiquitin Ligases from the MKRN Protein Family.
Journal: Biochemistry. Biokhimiia
Published: October 17, 2024
A case of 46,XX testicular disorders of sex development due to an apparent synonymous variant in the WT1 gene: difficulties of differential diagnosis of intrauterine virililzation syndrome in a girl
Journal: Problemy endokrinologii
Published: February 24, 2024
Clinical, hormonal and molecular genetic characteristics of patients with 46,XY disorders of sex development associated with variants in the HSD17B3 gene
Journal: Problemy endokrinologii
Published: November 30, 2023
Kalmann syndrome in monozygous twins as an isolated manifestation of the SOX10 gene defect
Journal: Problemy endokrinologii
Published: July 13, 2021
Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency: late diagnosis and gender reassignment in a two-year-old child
Journal: Problemy endokrinologii
Published: April 14, 2021
CDC73 mutations in young patients with primary hyperparathyroidism: A description of two clinical cases
Journal: Terapevticheskii arkhiv
Published: November 02, 2016
Familial partial lipodystrophy (Dunnigan syndrome) due to LMNA gene mutation: The first description of its clinical case in Russia
Journal: Terapevticheskii arkhiv
Published: June 02, 2015
TYPE 1 MULTIPLE ENDOCRINE NEOPLASIA SYNDROME AND FAMILIAL ISOLATED HYPERPARATHYROIDISM
Journal: Klinicheskaia meditsina
Published: January 01, 2015
Showing 1-9 of 9
Last Updated: 09/26/2026