Alexander V. Polyakov

4 Leninsky Avenue
Moscow, MOW 119049, Russian Federation

Last Updated: 09/26/2026

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Found 88 publications

Rapid ventricular pacing for induced hypotension in clipping of a large aneurysm of vertebrobasilar confluence

Rapid ventricular pacing for induced hypotension in clipping of a large aneurysm of vertebrobasilar confluence

Journal: Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko

Published: August 07, 2026

Microsurgical treatment of tentorial meningiomas: a systematic review

Microsurgical treatment of tentorial meningiomas: a systematic review

Journal: Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko

Published: August 07, 2026

Approaches in microsurgery for olfactory meningiomas: a systematic review and meta-analysis

Approaches in microsurgery for olfactory meningiomas: a systematic review and meta-analysis

Journal: Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko

Published: April 03, 2026

Rare SMA Patients: A Comprehensive Look at Clinical Features, Genetic Profiles and Therapeutic Approaches.

Rare SMA Patients: A Comprehensive Look at Clinical Features, Genetic Profiles and Therapeutic Approaches.

Journal: International journal of molecular sciences

Published: March 28, 2026

Experience in Molecular Genetic Diagnostics of Birt-Hogg-Dubé Syndrome: Characteristics of Identified Mutations and Evolution of the Methodological Approach.

Experience in Molecular Genetic Diagnostics of Birt-Hogg-Dubé Syndrome: Characteristics of Identified Mutations and Evolution of the Methodological Approach.

Journal: International journal of molecular sciences

Published: March 20, 2026

The electronic structures of β-phase (AlxGa1-x)2O3 studied using DFT calculations.

The electronic structures of β-phase (AlxGa1-x)2O3 studied using DFT calculations.

Journal: Physical chemistry chemical physics : PCCP

Published: January 27, 2026

Balanced Translocations Involving the DMD Gene as a Cause of Muscular Dystrophy in Female Children: A Description of Three Cases.

Balanced Translocations Involving the DMD Gene as a Cause of Muscular Dystrophy in Female Children: A Description of Three Cases.

Journal: International journal of molecular sciences

Published: September 05, 2025

Different Diagnoses, Common Ancestry: 22q11.2 Deletion Syndrome and Wiskott-Aldrich Syndrome in the Same Family.

Different Diagnoses, Common Ancestry: 22q11.2 Deletion Syndrome and Wiskott-Aldrich Syndrome in the Same Family.

Journal: Molecular syndromology

Published: June 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

Rare Cause 5q SMA: Molecular Genetic and Clinical Analyses of Intragenic Subtle Variants in the SMN Locus.

Rare Cause 5q SMA: Molecular Genetic and Clinical Analyses of Intragenic Subtle Variants in the SMN Locus.

Journal: Clinical genetics

Published: December 02, 2024

Optimized interdisciplinary approach in the treatment of maxillary sinus upper wall fractures in children

Optimized interdisciplinary approach in the treatment of maxillary sinus upper wall fractures in children

Journal: Vestnik otorinolaringologii

Published: November 15, 2024

Molecular genetic analysis of Rubinstein-Taybi syndrome in Russian patients.

Molecular genetic analysis of Rubinstein-Taybi syndrome in Russian patients.

Journal: Frontiers in genetics

Published: October 24, 2024

Showing 1-12 of 88

Last Updated: 09/26/2026