Maria M. Litvinova

Moscow, MOW 119435, Russian Federation

Last Updated: 09/26/2026

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Found 14 publications

Association of MMP9 and NOS3 Polymorphisms with Distinct Clinical Forms of Juvenile Scleroderma and Characteristics of Humoral Immunity.

Association of MMP9 and NOS3 Polymorphisms with Distinct Clinical Forms of Juvenile Scleroderma and Characteristics of Humoral Immunity.

Journal: International journal of molecular sciences

Published: December 29, 2025

Comprehensive Screening for Early Cancer Detection in Individuals With Genetic Predisposition.

Comprehensive Screening for Early Cancer Detection in Individuals With Genetic Predisposition.

Journal: JCO precision oncology

Published: August 20, 2025

Assessing germline TP53 mutations in cancer patients: insights into Li-Fraumeni syndrome and genetic testing guidelines.

Assessing germline TP53 mutations in cancer patients: insights into Li-Fraumeni syndrome and genetic testing guidelines.

Journal: Hereditary cancer in clinical practice

Published: December 06, 2024

Spectrum of PRSS1, SPINK1, CTRC, CFTR, and CPA1 Gene Variants in Chronic Pancreatitis Patients in Russia.

Spectrum of PRSS1, SPINK1, CTRC, CFTR, and CPA1 Gene Variants in Chronic Pancreatitis Patients in Russia.

Journal: Sovremennye tekhnologii v meditsine

Published: December 19, 2022

TLRs Gene Polymorphisms Associated with Pneumonia before and during COVID-19 Pandemic.

TLRs Gene Polymorphisms Associated with Pneumonia before and during COVID-19 Pandemic.

Journal: Diagnostics (Basel, Switzerland)

Published: November 21, 2022

A Unique Observation of a Patient with Vulto-van Silfhout-de Vries Syndrome.

A Unique Observation of a Patient with Vulto-van Silfhout-de Vries Syndrome.

Journal: Diagnostics (Basel, Switzerland)

Published: June 29, 2022

Physiological health indexes predict deterioration and mortality in patients with COVID-19: a comparative study.

Physiological health indexes predict deterioration and mortality in patients with COVID-19: a comparative study.

Journal: Aging

Published: November 04, 2021

A complicated case of calcium urolithiasis in a carrier of SLC7A9 gene mutation responsible for cystinuria

A complicated case of calcium urolithiasis in a carrier of SLC7A9 gene mutation responsible for cystinuria

Journal: Urologiia (Moscow, Russia : 1999)

Published: December 30, 2020

Association of CASR, CALCR, and ORAI1 Genes Polymorphisms With the Calcium Urolithiasis Development in Russian Population.

Association of CASR, CALCR, and ORAI1 Genes Polymorphisms With the Calcium Urolithiasis Development in Russian Population.

Journal: Frontiers in genetics

Published: November 05, 2020

Associations of Toll-like Receptor Gene Polymorphisms with NETosis Activity as Prognostic Criteria for the Severity of Pneumonia.

Associations of Toll-like Receptor Gene Polymorphisms with NETosis Activity as Prognostic Criteria for the Severity of Pneumonia.

Journal: Sovremennye tekhnologii v meditsine

Published: October 09, 2020

Molecular and genetic technologies for the diagnosis of monogenic forms of urinary stone disease: clinical cases

Molecular and genetic technologies for the diagnosis of monogenic forms of urinary stone disease: clinical cases

Journal: Urologiia (Moscow, Russia : 1999)

Published: June 30, 2020

Genetic aspects of primary hyperoxaluria: epidemiology, ethiology, pathogenesis, and clinical signs of the disorder

Genetic aspects of primary hyperoxaluria: epidemiology, ethiology, pathogenesis, and clinical signs of the disorder

Journal: Urologiia (Moscow, Russia : 1999)

Published: February 01, 2020

Showing 1-12 of 14

Last Updated: 09/26/2026