Irina E Guryanova
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Explore the profile of Irina E Guryanova including associated specialties, affiliations and a list of published articles.
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6
Citations
26
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Recent Articles
1.
Sharapova S, Golovataya E, Shepelevich E, Mareika Y, Guryanova I, Stegantseva M, et al.
Cent Eur J Immunol
. 2021 Mar;
45(4):507-510.
PMID: 33658897
Nijmegen breakage syndrome (NBS) is a rare autosomal recessive disorder, characterized by spontaneous chromosomal instability with predisposition to immunodeficiency and cancer. We present a repeated NBS in two sons from...
2.
Sharapova S, Haapaniemi E, Sakovich I, Rojas J, Gamez-Diaz L, Mareika Y, et al.
J Clin Immunol
. 2018 May;
38(4):471-474.
PMID: 29804237
No abstract available.
3.
Sharapova S, Valochnik A, Guryanova I, Sakovich I, Aleinikova O
Immunogenetics
. 2018 Mar;
70(9):613-617.
PMID: 29492593
Ataxia-telangiectasia (AT) is a rare neurodegenerative disease characterized by an early onset ataxia, oculocutaneous telangiectasia, immunodeficiency, recurrent infections, radio-sensitivity, and a predisposition to malignancy. We present the case of a...
4.
Sharapova S, Fedorova A, Pashchenko O, Vahliarskaya S, Guryanova I, Migas A, et al.
J Pediatr Hematol Oncol
. 2017 Mar;
39(4):e203-e206.
PMID: 28267077
Background: X-linked lymphoproliferative disease type I (XLP I) is caused by mutations in the SH2D1A gene and characterized mainly by hypogammaglobulinemia and abnormal response to Epstein-Barr virus with a high...
5.
Sharapova S, Chang E, Guryanova I, Proleskovskaya I, Fedorova A, Rutskaya E, et al.
Clin Immunol
. 2016 Jan;
163:108-10.
PMID: 26774591
Introduction: Here we present an unusual case of DNA ligase IV deficiency syndrome without dysmorphic facial findings and microcephaly complicated with Epstein-Barr virus-associated large B-cell lymphoma with the right lung...
6.
Sharapova S, Guryanova I, Pashchenko O, Kondratenko I, Kostyuchenko L, Rodina Y, et al.
J Clin Immunol
. 2015 Nov;
36(1):46-55.
PMID: 26596586
Background: Omenn syndrome [Mendelian Inheritance (OMIM 603554)] is a genetic disease of the immune system, characterized by the presence of fatal generalized severe erythroderma, lymphoadenopathy, eosinophilia and profound immunodeficiency. Objective:...