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Svetlana O. Sharapova
Svetlana O. Sharapova
PhD, Belarusian Research Center for Pediatric Oncology, Hematology and Immunology
Підтверджена електронна адреса в oncology.by
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Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: a cohort study
E Elkaim, B Neven, J Bruneau, K Mitsui-Sekinaka, A Stanislas, L Heurtier, ...
Journal of Allergy and Clinical Immunology 138 (1), 210-218. e9, 2016
4292016
Disease evolution and response to rapamycin in activated phosphoinositide 3-kinase δ syndrome: the european society for immunodeficiencies-activated phosphoinositide 3-kinase δ …
ME Maccari, H Abolhassani, A Aghamohammadi, A Aiuti, O Aleinikova, ...
Frontiers in immunology 9, 543, 2018
3482018
Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score
VK Tesch, H Abolhassani, B Shadur, J Zobel, Y Mareika, S Sharapova, ...
Journal of Allergy and Clinical Immunology 145 (5), 1452-1463, 2020
1262020
Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations
J Thalhammer, G Kindle, A Nieters, S Rusch, MRJ Seppänen, A Fischer, ...
Journal of Allergy and Clinical Immunology 148 (5), 1332-1341. e5, 2021
922021
Heterozygous FOXN1 variants cause low TRECs and severe T cell lymphopenia, revealing a crucial role of FOXN1 in supporting early thymopoiesis
M Bosticardo, Y Yamazaki, J Cowan, G Giardino, C Corsino, G Scalia, ...
The American Journal of Human Genetics 105 (3), 549-561, 2019
562019
Treatment of severe forms of LPS-responsive beige-like anchor protein deficiency with allogeneic hematopoietic stem cell transplantation
MG Seidel, K Böhm, F Dogu, A Worth, A Thrasher, B Florkin, ...
Journal of Allergy and Clinical Immunology 141 (2), 770-775. e1, 2018
542018
Monogenic early-onset lymphoproliferation and autoimmunity: natural history of STAT3 gain-of-function syndrome
JW Leiding, TP Vogel, VGJ Santarlas, R Mhaskar, MR Smith, A Carisey, ...
Journal of Allergy and Clinical Immunology 151 (4), 1081-1095, 2023
452023
Prevalence and clinical challenges among adult primary immunodeficiency patients with RAG deficiency
D Lawless, CB Geier, JR Farmer, HA Lango, D Thwaites, F Atschekzei, ...
The Journal of allergy and clinical immunology 141 (6), 2303, 2018
402018
Late-onset combined immune deficiency associated to skin granuloma due to heterozygous compound mutations in RAG1 gene in a 14 years old male
SO Sharapova, A Migas, I Guryanova, S Aleshkevich, S Kletski, ...
Human Immunology 74 (1), 18-22, 2013
382013
Heterozygous activating mutation in RAC2 causes infantile-onset combined immunodeficiency with susceptibility to viral infections
SO Sharapova, E Haapaniemi, IS Sakovich, LV Kostyuchenko, A Donko, ...
Clinical Immunology 205, 1-5, 2019
302019
Geographical Distribution, Incidence, Malignancies, and Outcome of 136 Eastern Slavic Patients With Nijmegen Breakage Syndrome and NBN Founder Variant c …
SO Sharapova, OE Pashchenko, AV Bondarenko, SS Vakhlyarskaya, ...
Frontiers in Immunology 11, 602482, 2021
242021
Molecular characteristics, clinical and immunologic manifestations of 11 children with Omenn syndrome in East Slavs (Russia, Belarus, Ukraine)
SO Sharapova, IE Guryanova, OE Pashchenko, IV Kondratenko, ...
Journal of clinical immunology 36, 46-55, 2016
242016
Partial RAG deficiency in humans induces dysregulated peripheral lymphocyte development and humoral tolerance defect with accumulation of T-bet+ B cells
K Csomos, B Ujhazi, P Blazso, JL Herrera, CM Tipton, T Kawai, S Gordon, ...
Nature immunology 23 (8), 1256-1272, 2022
192022
Phenotype, genotype, treatment, and survival outcomes in patients with X-linked inhibitor of apoptosis deficiency
L Yang, C Booth, C Speckmann, MG Seidel, AJJ Worth, G Kindle, ...
Journal of Allergy and Clinical Immunology 150 (2), 456-466, 2022
182022
Expanding the nude SCID/CID phenotype associated with FOXN1 homozygous, compound heterozygous, or heterozygous mutations
G Giardino, SO Sharapova, P Ciznar, F Dhalla, L Maragliano, ...
Journal of Clinical Immunology 41, 756-768, 2021
162021
Next generation sequencing revealed DNA ligase IV deficiency in a “developmentally normal” patient with massive brain Epstein–Barr virus-positive diffuse large B-cell lymphoma
SO Sharapova, EY Chang, IE Guryanova, IV Proleskovskaya, ...
Clinical Immunology 163, 108-110, 2016
162016
Hypomorphic RAG deficiency: impact of disease burden on survival and thymic recovery argues for early diagnosis and HSCT
C Schuetz, J Gerke, M Ege, J Walter, M Kusters, A Worth, JA Kanakry, ...
Blood 141 (7), 713-724, 2023
142023
Disease progression of WHIM syndrome in an international cohort of 66 pediatric and adult patients
CB Geier, M Ellison, R Cruz, S Pawar, A Leiss-Piller, K Zmajkovicova, ...
Journal of clinical immunology 42 (8), 1748-1765, 2022
142022
The Clinical and Genetic Spectrum of 82 Patients With RAG Deficiency Including a c.256_257delAA Founder Variant in Slavic Countries
SO Sharapova, M Skomska-Pawliszak, YA Rodina, B Wolska-Kuśnierz, ...
Frontiers in immunology 11, 900, 2020
142020
Simple measurement of IgA predicts immunity and mortality in ataxia-telangiectasia
S Zielen, RP Duecker, S Woelke, H Donath, S Bakhtiar, A Buecker, ...
Journal of clinical immunology 41, 1878-1892, 2021
132021
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