Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Immune deficiency disorder"'
Akademický článek
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Autor:
Jan R. Dörr, Anne Thorwarth, Agnieszka Mizia-Malarz, Josefine Radke, Anna Tietze, Pablo Hernáiz-Driever, Denise Horn, Alexander Gratopp, Angelika Eggert, Hedwig E. Deubzer
Publikováno v:
Children, Vol 8, Iss 6, p 469 (2021)
We here report the case of a 2-year-old patient with a primary central nervous system lymphoma of B-cell origin. Due to their past medical history of repeated respiratory tract infections and the marked chemotherapy-associated toxicity and infectious
Externí odkaz:
https://doaj.org/article/f0982dc5966a42159874bf1c22ec4a61
Autor:
Pauline A. van Schouwenburg, Hanna IJspeert, Ingrid Pico-Knijnenburg, Virgil A. S. H. Dalm, P. Martin van Hagen, David van Zessen, Andrew P. Stubbs, Smita Y. Patel, Mirjam van der Burg
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Common variable immune deficiency disorder (CVID) is the most clinically relevant cause of antibody failure. It is a highly heterogeneous disease with different underlying etiologies. CVID has been associated with a quantitative B cell defect, howeve
Externí odkaz:
https://doaj.org/article/e6d89f4f38df4d03befd245ad4c51274
Publikováno v:
African Journal of Economic and Management Studies, 2010, Vol. 1, Issue 2, pp. 197-210.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/20400701011073491
Autor:
Laurel Wolf, Kelli W. Williams
Publikováno v:
Pediatrics. 148:S67-S68
Publikováno v:
QJM: An International Journal of Medicine. 113
Introduction Despite efforts, primary immunodeficiency disorders (PIDs) are still under estimated. Predominantly antibody deficiencies (PADs) account for approximately two-thirds of all PIDs. We sought to screen for immunoglobulin deficiency among Eg
Publikováno v:
Scholar: Pilot and Validation Studies. 1:11-13
Background: Common variable immunodeficiency (CVID) is a heterogeneous group of primary immune deficiency disorders that may be characterized by heightened susceptibility to gastrointestinal (GI) infection. GI conditions manifest in 20 to 50% of CVID
Autor:
Alexandra F. Freeman
Publikováno v:
Journal of the Pediatric Infectious Diseases Society. 7:S79-S82
Hematopoietic stem cell transplantation (HSCT) has been the standard of care for infants with severe combined immunodeficiency (SCID) for several decades due to the dismal prognosis early in life without immune reconstitution. In recent years, as HSC
Publikováno v:
Journal of the Pediatric Infectious Diseases Society
Chronic Granulomatous Disease is one of the classic primary immunodeficiencies of childhood. While the incidence and severity of bacterial and fungal infections have been greatly reduced in this patient population, much remains to be learned about th
Publikováno v:
Journal of the Pediatric Infectious Diseases Society. 9(1)