Irina V. Kondratenko

Moscow, MOW, Russian Federation

Last Updated: 09/26/2026

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Found 14 publications

Wiskott-Aldrich syndrome: a study of 577 patients defines the genotype as a biomarker for disease severity and survival.

Wiskott-Aldrich syndrome: a study of 577 patients defines the genotype as a biomarker for disease severity and survival.

Journal: Blood

Published: July 10, 2023

Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity.

Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity.

Journal: The Journal of allergy and clinical immunology

Published: April 08, 2023

Allogeneic Hematopoietic Stem Cell Transplantation Activity in Inborn Errors of Immunity in Russian Federation.

Allogeneic Hematopoietic Stem Cell Transplantation Activity in Inborn Errors of Immunity in Russian Federation.

Journal: Journal of clinical immunology

Published: December 19, 2022

Care of patients with inborn errors of immunity in thirty J Project countries between 2004 and 2021.

Care of patients with inborn errors of immunity in thirty J Project countries between 2004 and 2021.

Journal: Frontiers in immunology

Published: August 30, 2022

Geographical Distribution, Incidence, Malignancies, and Outcome of 136 Eastern Slavic Patients With Nijmegen Breakage Syndrome and NBN Founder Variant c.657_661del5.

Geographical Distribution, Incidence, Malignancies, and Outcome of 136 Eastern Slavic Patients With Nijmegen Breakage Syndrome and NBN Founder Variant c.657_661del5.

Journal: Frontiers in immunology

Published: September 03, 2020

Primary Immunodeficiencies in Russia: Data From the National Registry.

Primary Immunodeficiencies in Russia: Data From the National Registry.

Journal: Frontiers in immunology

Published: April 03, 2020

The Clinical and Genetic Spectrum of 82 Patients With RAG Deficiency Including a c.256_257delAA Founder Variant in Slavic Countries.

The Clinical and Genetic Spectrum of 82 Patients With RAG Deficiency Including a c.256_257delAA Founder Variant in Slavic Countries.

Journal: Frontiers in immunology

Published: March 04, 2020

Next generation sequencing analysis of consecutive Russian patients with clinical suspicion of inborn errors of immunity.

Next generation sequencing analysis of consecutive Russian patients with clinical suspicion of inborn errors of immunity.

Journal: Clinical genetics

Published: January 15, 2020

Mitochondrial permeability transition pore is involved in oxidative burst and NETosis of human neutrophils.

Mitochondrial permeability transition pore is involved in oxidative burst and NETosis of human neutrophils.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: September 09, 2019

ATM mutation spectrum in Russian children with ataxia-telangiectasia.

ATM mutation spectrum in Russian children with ataxia-telangiectasia.

Journal: European journal of medical genetics

Published: December 08, 2018

Novel Mutations in SH2D1A Gene in X-linked Lymphoproliferative Syndrome, Diagnosed After B-Cell Non-Hodgkin Lymphoma.

Novel Mutations in SH2D1A Gene in X-linked Lymphoproliferative Syndrome, Diagnosed After B-Cell Non-Hodgkin Lymphoma.

Journal: Journal of pediatric hematology/oncology

Published: March 08, 2017

Recent thymic emigrants, T regulatory cells, and BAFF level in children with X-linked agammaglobulinaemia in association with chronic respiratory disease.

Recent thymic emigrants, T regulatory cells, and BAFF level in children with X-linked agammaglobulinaemia in association with chronic respiratory disease.

Journal: Allergologia et immunopathologia

Published: December 11, 2016

Showing 1-12 of 14

Last Updated: 09/26/2026