Victoria D. Sherman

Moskvorechie St, 1
Moscow, MOW 115522, Russian Federation

Last Updated: 09/26/2026

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Found 10 publications

L467F;F508del Complex Allele in a Heterozygous State with CFTRdele2,3: What to Expect from CFTR Modulators?

L467F;F508del Complex Allele in a Heterozygous State with CFTRdele2,3: What to Expect from CFTR Modulators?

Journal: International journal of molecular sciences

Published: October 23, 2025

Clinical Presentation of the c.3844T>C (p.Trp1282Arg, W1282R) Variant in Russian Cystic Fibrosis Patients.

Clinical Presentation of the c.3844T>C (p.Trp1282Arg, W1282R) Variant in Russian Cystic Fibrosis Patients.

Journal: Genes

Published: August 14, 2020

Vitamin D Status in Russian Children and Adolescents: Contribution of Genetic and Exogenous Factors.

Vitamin D Status in Russian Children and Adolescents: Contribution of Genetic and Exogenous Factors.

Journal: Frontiers in pediatrics

Published: July 14, 2020

Analysis of CFTR Mutation Spectrum in Ethnic Russian Cystic Fibrosis Patients.

Analysis of CFTR Mutation Spectrum in Ethnic Russian Cystic Fibrosis Patients.

Journal: Genes

Published: March 30, 2020

Clinical and genetic characterization of patients with cystic fibrosis and functional assessment of the chloride channel with the pathogenic variant c.831G>A (p.Trp277*), described for the first time.

Clinical and genetic characterization of patients with cystic fibrosis and functional assessment of the chloride channel with the pathogenic variant c.831G>A (p.Trp277*), described for the first time.

Journal: Gene

Published: March 23, 2020

Newborn Screening for Cystic Fibrosis in Russia: A Catalyst for Improved Care.

Newborn Screening for Cystic Fibrosis in Russia: A Catalyst for Improved Care.

Journal: International journal of neonatal screening

Published: January 26, 2020

Dynamics of indicators of vitamin D status in children with cystic fibrosis of the Moscow region for 2016-2018

Dynamics of indicators of vitamin D status in children with cystic fibrosis of the Moscow region for 2016-2018

Journal: Voprosy pitaniia

Published: October 05, 2019

Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G>A (p.Glu92Lys, E92K) mutations in North Caucasus.

Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G>A (p.Glu92Lys, E92K) mutations in North Caucasus.

Journal: BMC medical genetics

Published: September 27, 2018

The experience of application of target sequencing in molecular diagnostic of mucoviscidosis.

The experience of application of target sequencing in molecular diagnostic of mucoviscidosis.

Journal: Klinicheskaia laboratornaia diagnostika

Published: November 30, 2016

High prevalence of W1282x mutation in cystic fibrosis patients from Karachay-Cherkessia.

High prevalence of W1282x mutation in cystic fibrosis patients from Karachay-Cherkessia.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: September 30, 2015

Showing 1-10 of 10

Last Updated: 09/26/2026