S. Aleshkevich

Genetic defects in patients with primary immunodeficiencies in the Republic of Belarus

M. Belevtsev, O. Aleinikova, A. Migas, 2020, Proceedings of the National Academy of Sciences of Belarus, Medical series.

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.

Abstracts from the 10th C1-inhibitor deficiency workshop

William H. Yang, A. Szilágyi, M. Margaglione, 2017, Allergy, Asthma & Clinical Immunology.

Demographic characteristics of patients with genetically confirmed hereditary angioedema in the Republic of Belarus

M. Belevtsev, Y. Zharankova, I. Guryanova, 2022, Immunopathology, Allergology, Infectology.

Quantitative determination of circular DNA fragments of the T- and B-cell receptor TREC/KREC in patients with ataxia-telangiectasia with a mutation in the ATM gene

M. Belevtsev, S. Sharapova, I. Sakovich, 2022, Immunopathology, Allergology, Infectology.

Late-onset combined immune deficiency associated to skin granuloma due to heterozygous compound mutations in RAG1 gene in a 14 years old male.

A. Durandy, M. Belevtsev, A. Migas, 2013, Human immunology.

Non-Hodgkin Lymphoma in Children with Primary Immunodeficiencies: Clinical Manifestations, Diagnosis, and Management, Belarusian Experience

M. Belevtsev, O. Aleinikova, A. Fedorova, 2015 .

Monogenic Early-Onset Lymphoproliferation and Autoimmunity: The Natural History of STAT3 GOF Syndrome.

K. Schwarz, M. Weinrich, F. Rieux-Laucat, 2022, The Journal of allergy and clinical immunology.

A Novel Transmembrane CXCR4 Variant That Expands the WHIM Genotype-Phenotype Paradigm.

T. Tarrant, A. Badarau, Sumit Pawar, 2024, Blood Advances.

The use of next generation sequencing technologies for the diagnosis of inborn errors of immunity

S. Sharapova, K. Y. Skapavets, I. Guryanova, 2023, Pediatric Hematology/Oncology and Immunopathology.