Natalia Y. Kalinchenko

Moscow, MOW, Russian Federation

Last Updated: 09/26/2026

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Found 32 publications

Dyshormonogenetic goiter in a patient with congenital hypothyroidism: clinical, morphological and genetic features

Dyshormonogenetic goiter in a patient with congenital hypothyroidism: clinical, morphological and genetic features

Journal: Arkhiv patologii

Published: June 18, 2026

Clinical practice guidelines "Congenital adrenal hyperplasia in children" with comments

Clinical practice guidelines "Congenital adrenal hyperplasia in children" with comments

Journal: Problemy endokrinologii

Published: March 26, 2026

Complications of Pseudohypoparathyroidism and Congenital Forms of Hypoparathyroidism in Children

Complications of Pseudohypoparathyroidism and Congenital Forms of Hypoparathyroidism in Children

Journal: Problemy endokrinologii

Published: December 26, 2025

A familial case of FLAD1 protein deficiency associated with impaired adrenal steroidogenesis.

A familial case of FLAD1 protein deficiency associated with impaired adrenal steroidogenesis.

Journal: JCI insight

Published: August 05, 2025

Does everyone need to take vitamin D? High prevalence of CYP24A1 deficiency in the Russian population.

Does everyone need to take vitamin D? High prevalence of CYP24A1 deficiency in the Russian population.

Journal: Problemy endokrinologii

Published: January 23, 2025

Salivary steroid profile investigation by high performance liquid chromatography-tandem mass spectrometry in children with congenital adrenal hyperplasia

Salivary steroid profile investigation by high performance liquid chromatography-tandem mass spectrometry in children with congenital adrenal hyperplasia

Journal: Problemy endokrinologii

Published: January 10, 2025

Cushing's disease in a 15-year-old boy, manifesting in prepubertal age

Cushing's disease in a 15-year-old boy, manifesting in prepubertal age

Journal: Problemy endokrinologii

Published: December 23, 2024

Clinical, hormonal and molecular genetic characteristics of 18 cases of disorders of sex development (DSD) 46,XY associated with variants in the SRD5A2 gene

Clinical, hormonal and molecular genetic characteristics of 18 cases of disorders of sex development (DSD) 46,XY associated with variants in the SRD5A2 gene

Journal: Problemy endokrinologii

Published: December 03, 2024

Out-of-frame Translation Rescues a Loss-of-function Variant in a Novel TBCE Phenotype.

Out-of-frame Translation Rescues a Loss-of-function Variant in a Novel TBCE Phenotype.

Journal: The Journal of clinical endocrinology and metabolism

Published: September 19, 2024

Microcephalic osteodysplastic primordial dwarfism type II (MOPD II): clinical case

Microcephalic osteodysplastic primordial dwarfism type II (MOPD II): clinical case

Journal: Problemy endokrinologii

Published: September 11, 2024

Clinical polymorphism of primary hyperparathyroidism in children

Clinical polymorphism of primary hyperparathyroidism in children

Journal: Problemy endokrinologii

Published: July 15, 2024

Combination approach for CDC73-related parathyroid carcinoma in an adolescent female patient: a case report and literature review.

Combination approach for CDC73-related parathyroid carcinoma in an adolescent female patient: a case report and literature review.

Journal: Therapeutic advances in medical oncology

Published: December 14, 2023

Showing 1-12 of 32

Last Updated: 09/26/2026