Alexander A. Pushkov

Moscow, MOW, Russian Federation

Last Updated: 09/26/2026

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Found 21 publications

Trans-2,3-enoyl-CoA reductase-like-related catecholaminergic polymorphic ventricular tachycardia in a child: Clinical course and management outcomes.

Trans-2,3-enoyl-CoA reductase-like-related catecholaminergic polymorphic ventricular tachycardia in a child: Clinical course and management outcomes.

Journal: Annals of pediatric cardiology

Published: February 12, 2026

A Unique Case of a Child with Two Rare Hereditary Diseases: Familial Dilated Cardiomyopathy and Arterial Calcification.

A Unique Case of a Child with Two Rare Hereditary Diseases: Familial Dilated Cardiomyopathy and Arterial Calcification.

Journal: International journal of molecular sciences

Published: May 06, 2025

Genetic and Clinical Features of Schimke Immuno-Osseous Dysplasia: Single-Centre Retrospective Study of 21 Unrelated Paediatric Patients over a Period of 20 Years.

Genetic and Clinical Features of Schimke Immuno-Osseous Dysplasia: Single-Centre Retrospective Study of 21 Unrelated Paediatric Patients over a Period of 20 Years.

Journal: International journal of molecular sciences

Published: December 09, 2024

Case Series: Genetic mimics of hypertrophic cardiomyopathy in elderly.

Case Series: Genetic mimics of hypertrophic cardiomyopathy in elderly.

Journal: Frontiers in cardiovascular medicine

Published: August 19, 2024

Mutations in Mismatch Repair Genes and Microsatellite Instability Status in Pancreatic Cancer.

Mutations in Mismatch Repair Genes and Microsatellite Instability Status in Pancreatic Cancer.

Journal: Cancers

Published: March 25, 2024

Genotype-Phenotype Correlations in 293 Russian Patients with Causal Fabry Disease Variants.

Genotype-Phenotype Correlations in 293 Russian Patients with Causal Fabry Disease Variants.

Journal: Genes

Published: September 22, 2023

Clinical features of pediatric Danon disease and the importance of early diagnosis.

Clinical features of pediatric Danon disease and the importance of early diagnosis.

Journal: International journal of cardiology

Published: February 15, 2023

Targeted NGS in Diagnostics of Genodermatosis Characterized by the Epidermolysis Bullosa Symptom Complex in 268 Russian Children.

Targeted NGS in Diagnostics of Genodermatosis Characterized by the Epidermolysis Bullosa Symptom Complex in 268 Russian Children.

Journal: International journal of molecular sciences

Published: September 27, 2022

Clinical and Genetic Characteristics of Pediatric Patients with Hypophosphatasia in the Russian Population.

Clinical and Genetic Characteristics of Pediatric Patients with Hypophosphatasia in the Russian Population.

Journal: International journal of molecular sciences

Published: September 05, 2022

Comparison of disease phenotypes and mechanistic insight on causal variants in patients with DADA2.

Comparison of disease phenotypes and mechanistic insight on causal variants in patients with DADA2.

Journal: The Journal of allergy and clinical immunology

Published: June 30, 2022

Genetic Landscape of Nephropathic Cystinosis in Russian Children.

Genetic Landscape of Nephropathic Cystinosis in Russian Children.

Journal: Frontiers in genetics

Published: January 26, 2022

The prevalence of Fabry disease among 1009 unrelated patients with hypertrophic cardiomyopathy: a Russian nationwide screening program using NGS technology.

The prevalence of Fabry disease among 1009 unrelated patients with hypertrophic cardiomyopathy: a Russian nationwide screening program using NGS technology.

Journal: Orphanet journal of rare diseases

Published: October 13, 2021

Showing 1-12 of 21

Last Updated: 09/26/2026