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pro vyhledávání: '"Sirje Velbri"'
Autor:
Sirje Velbri, Ülle Einberg
Publikováno v:
Pediatric Immunology ISBN: 9783030212612
X-linked agammaglobulinemia ( XLA) is a severe form of primary antibody deficiency characterized by increased susceptibility to bacterial infections
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5040667607fe0bcb15811ae3b043df6b
https://doi.org/10.1007/978-3-030-21262-9_8
https://doi.org/10.1007/978-3-030-21262-9_8
Autor:
László, Maródi, Sirje, Velbri
Publikováno v:
Annals of the New York Academy of Sciences. 1238
Primary immunodeficiencies (PIDs) have now become recognized as a worldwide health problem. Rapid development of immunological and genetic technologies has led to the discovery of more than 200 PIDs and more than 150 disease-related genes. Progress i
Autor:
Hana Hansikova, Carla M. Koehler, Jan Hadač, Anna Sediva, Jiří Zeman, Hans D. Ochs, Takeshi Futatani, Lenka Mrázová, Karin Roesch, Lenka Dvořáková, C. I. Edvard Smith, Sirje Velbri, Ales Janda, A. Charlotta Asplund, Kathleen E. Sullivan
Publikováno v:
Journal of clinical immunology. 27(6)
X-linked agammaglobulinemia (XLA) is characterized by low levels of B-lymphocytes with early-onset, recurrent, microbial infections occasionally causing neurological symptoms. We observed an atypical clinical course of XLA, complicated since early ch