I. Kondratenko

发表

Mycobacterial infections in primary immunodeficiency patients.

E. Galkina, I. Kondratenko, A. Bologov, 2007, Advances in experimental medicine and biology.

The experience of hematopoietic stem cell transplantation in primary immunodeficiencies in the Russian Children's Clinical Hospital

I. Kondratenko, A. Maschan, E. Machneva, 2019, Pediatric Hematology/Oncology and Immunopathology.

Genetic and demographic features of X-linked agammaglobulinemia in Eastern and Central Europe: a cohort study.

M. van der Burg, J. V. van Dongen, L. Notarangelo, 2009, Molecular immunology.

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

B. Chernyak, I. Kondratenko, R. Zinovkin, 2020, Biochimica et biophysica acta. Molecular basis of disease.

Genetic characteristics of eighty-seven patients with the Wiskott-Aldrich syndrome.

M. van der Burg, B. Tóth, N. Kutukculer, 2011, Molecular immunology.

Hematologically important mutations: X-linked chronic granulomatous disease (third update).

S. Holland, T. Ariga, D. Kuhns, 1997, Blood cells, molecules & diseases.

Nanohyperthermia of malignant tumors. II. In vivo tumor heating with manganese perovskite nanoparticles.

I. Kondratenko, L. Bubnovskaya, S. Osinsky, 2012, Experimental oncology.

Gene therapy for Wiskott-Aldrich syndrome-long - Term efficacy and genotoxicity (Science Translational Medicine)

D. Steinemann, A. Schambach, W. Al-Herz, 2014 .

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

I. Kondratenko, O. Aleinikova, A. Migas, 2018, Allergologia et immunopathologia.

Lack of specific antibody response in common variable immunodeficiency (CVID) associated with failure in production of antigen‐specific memory T cells

J. Farrant, I. Kondratenko, A. Webster, 1997, Clinical and experimental immunology.

Correction of Wiskott-Aldrich Syndrome by Hematopoietic Stem Cell Gene Therapy

J. Orange, W. Al-Herz, C. Klein, 2010 .

RAACI’s and NAEPID’s position paper: vaccination of patients with PID and HAE against COVID-19.

M. Khaitov, I. Kondratenko, A. Shcherbina, 2021, Russian Journal of Allergy.

ATM mutation spectrum in Russian children with ataxia-telangiectasia.

A. Sokolenko, E. Imyanitov, I. Kondratenko, 2019, European journal of medical genetics.

Results of allogeneic hematopoietic stem cell transplantation in patients with chronic granulomatous disease at the Russian Children’s Clinical Hospital

I. Kondratenko, E. Machneva, E. Skorobogatova, 2020, Russian Journal of Pediatric Hematology and Oncology.

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

J. Walter, I. Tuzankina, I. Kondratenko, 2021, Frontiers in Immunology.

Gene Therapy for Wiskott-Aldrich Syndrome—Long-Term Efficacy and Genotoxicity

Michael Rothe, Christof von Kalle, Raffaele Fronza, 2014, Science Translational Medicine.

Stem-cell gene therapy for the Wiskott-Aldrich syndrome.

Christof von Kalle, Christoph Klein, Rainer Blasczyk, 2010, The New England journal of medicine.

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

M. van der Burg, L. Notarangelo, J. Walter, 2020, Frontiers in Immunology.

Haematological complications of X-linked lymphoproliferative syndrome type 1 and 2

I. Kondratenko, A. Shcherbina, L. Shelikhova, 2020, Pediatric Hematology/Oncology and Immunopathology.

Nijmegen breakage syndrome: clinical characteristics and mutation analysis in eight unrelated Russian families.

K. Cerosaletti, O. Evgrafov, R. Gatti, 2002, The Journal of pediatrics.

Andrew P. Stubbs, M. van der Burg, E. Mejstrikova, 2014, Journal of Allergy and Clinical Immunology.

Gross deletions involving IGHM, BTK, or Artemis: a model for genomic lesions mediated by transposable elements.

M. van der Burg, M. V. van Zelm, J. V. van Dongen, 2008, American journal of human genetics.

Primary Immunodeficiencies in Russia: Data From the National Registry

T. B. Pavlova, E. M. Kamaltynova, A. V. Gorenkova, 2020, Frontiers in Immunology.

Successful SCT for Nijmegen breakage syndrome

A. Gennery, W. Młynarski, M. Führer, 2010, Bone Marrow Transplantation.

Molecular Characteristics, Clinical and Immunologic Manifestations of 11 Children with Omenn Syndrome in East Slavs (Russia, Belarus, Ukraine)

Y. Rodina, I. Kondratenko, L. Chernyshova, 2015, Journal of Clinical Immunology.

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

A. Sokolenko, E. Imyanitov, I. Kondratenko, 2020, Clinical genetics.

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

J. Casanova, A. Šedivá, Y. Rodina, 2022, Frontiers in Immunology.

Nijmegen breakage syndrome.

I. Kondratenko, A. Bologov, A. Polyakov, 2007, Advances in experimental medicine and biology.

657del5 mutation in the gene for Nijmegen breakage syndrome (NBS1) in a cohort of Russian children with lymphoid tissue malignancies and controls

O. Evgrafov, I. Kondratenko, S. Tverskaya, 2003, American journal of medical genetics. Part A.

Fifteen Years of the J Project

A. Šedivá, J. Litzman, I. Tuzankina, 2019, Journal of Clinical Immunology.

Nanohyperthermia of malignant tumors. I. Lanthanum-strontium manganite magnetic fluid as potential inducer of tumor hyperthermia.

I. Kondratenko, A. Yelenich, L. Bubnovskaya, 2011, Experimental oncology.

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

I. Kondratenko, O. Aleinikova, A. Migas, 2017, Journal of pediatric hematology/oncology.

Efficacy of Gene Therapy for Wiskott-Aldrich-Syndrome

W. Al-Herz, C. Klein, A. Schwarzer, 2011 .

Non-Malignant Lymphoproliferation

I. Kondratenko, A. Bologov, O. Pashchenko, 2019, Pediatric Immunology.

Siblings Presenting with Mild and Severe Lymphoproliferation

I. Kondratenko, O. Pashchenko, Svetlana Vakhlyrskaya, 2019, Pediatric Immunology.

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

Y. Skvortsova, I. Kondratenko, E. Skorobogatova, 2023, Journal of Clinical Immunology.

Analysis of toll-like receptor-dependent production of proinflammatory cytokines in vitro by human peripheral blood mononuclears of donors and patients with primary immunodeficiency

L. V. Koval’chuk, I. Kondratenko, A. A. Bologov, 2007, Bulletin of Experimental Biology and Medicine.

Activated Phosphoinositide 3-Kinase δ Syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity.

A. Schulz, V. Lougaris, A. Plebani, 2023, Journal of Allergy and Clinical Immunology.

[Effect of toll-like receptors (TLR) ligands on in vitro synthesis of proinflammatory cytokines by peripheral blood mononuclear cells from healthy persons and from patients with common variable immunodeficiency].

L. V. Koval’chuk, I. Kondratenko, A. A. Bologov, 2007, Zhurnal mikrobiologii, epidemiologii, i immunobiologii.

CHARACTERISTICS OF PATIENTS WITH PRIMARY IMMUNODEFICIENCY STATES IN THE RUSSIAN FEDERATION: FROM BIRTH TO OLD AGE

T. B. Pavlova, E. M. Kamaltynova, M. A. Bolkov, 2019, Pediatria. Journal named after G.N. Speransky.