Zobrazeno 1 - 10
of 22
pro vyhledávání: '"KX antigen"'
Publikováno v:
Transfusion medicine and hemotherapy 49(1), 4-12 (2022). doi:10.1159/000521417
Transfus Med Hemother
Transfusion medicine and hemotherapy, 49(1):4-12
Transfus Med Hemother
Transfusion medicine and hemotherapy, 49(1):4-12
Background: McLeod syndrome (MLS) is an X-linked multisystemic progressive disorder caused by loss of function mutations in the XK gene. The rare blood group phenotype of MLS patients with absent Kx antigen requires the support of specialized transfu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03587ac7e2795ac44e309d746fe3fafc
https://doi.org/10.1159/000521417
https://doi.org/10.1159/000521417
Autor:
Watkins Casey E, Litchfield John, Song Eunkyung, Jaishankar Gayatri B, Misra Niva, Holla Nikhil, Duffourc Michelle, Krishnaswamy Guha
Publikováno v:
Clinical and Molecular Allergy, Vol 9, Iss 1, p 13 (2011)
Abstract Chronic Granulomatous Disease (CGD), a disorder of the NADPH oxidase system, results in phagocyte functional defects and subsequent infections with bacterial and fungal pathogens (such as Aspergillus species and Candida albicans). Deletions
Externí odkaz:
https://doaj.org/article/999abda06da8411cb6be03452e42754c
Akademický článek
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Autor:
Nikhil Holla, Guha Krishnaswamy, Gayatri Bala Jaishankar, Casey E Watkins, John Litchfield, Eunkyung Song, Michelle M. Duffourc, Niva Misra
Publikováno v:
Clinical and Molecular Allergy, Vol 9, Iss 1, p 13 (2011)
Clinical and Molecular Allergy : CMA
Clinical and Molecular Allergy : CMA
Chronic Granulomatous Disease (CGD), a disorder of the NADPH oxidase system, results in phagocyte functional defects and subsequent infections with bacterial and fungal pathogens (such as Aspergillus species and Candida albicans). Deletions and misse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48b9192436ebe59934ae080ed53be900
http://www.clinicalmolecularallergy.com/content/9/1/13
http://www.clinicalmolecularallergy.com/content/9/1/13
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Blood. 74:1826-1835
The rare McLeod blood group phenotype is characterized by weak Kell antigens, lack of the common Kx antigen, and acanthocytic morphology. Previous studies that did not detect membrane or cytoskeletal protein abnormalities suggested a lipid disturbanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac424d05891da30ec31e930f1a63928d
https://doi.org/10.1182/blood.v74.5.1826.1826
https://doi.org/10.1182/blood.v74.5.1826.1826
Publikováno v:
Vox Sanguinis. 31:356-362
Leukocytes of nine unrelated boys with X-linked chronic granulomatous disease lack Kx antigen. In three of these cases, the red cells also lack Kx and have the McLeod phenotype and abnormal morphology. X-linked chronic granulomatous disease CGD can t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0287dfdf3e54ca24d2c7c66178357b67
https://doi.org/10.1111/j.1423-0410.1976.tb04659.x
https://doi.org/10.1111/j.1423-0410.1976.tb04659.x
Publikováno v:
Revue Francaise de Transfusion et Immuno-hématologie. 23:305-317
An 18 year old man has red cells of the McLeod phenotype in the Kell system but does not have chronic granulomatous disease. His red cells show acanthocytic morphology and there is evidence of a compensated hemolytic state. Following an accident he w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e0fef421f63701a01a8dd56aa08bf65
https://doi.org/10.1016/s0338-4535(80)80134-6
https://doi.org/10.1016/s0338-4535(80)80134-6
Auto anti-Kpb associated with weakened antigenicity in the Kell blood group system: a second example
Publikováno v:
Transfusion. 19:197-202
An 84-year-old woman with intestinal bleeding had marked reduction of red blood cell antigenicity in the Kell system, and a positive direct antiglobulin test caused by auto-anti-Kpb. KX antigen activity of her cell was increased, an observation which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a36023d26527f57c14b9c712badecff
https://doi.org/10.1046/j.1537-2995.1979.19279160294.x
https://doi.org/10.1046/j.1537-2995.1979.19279160294.x
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9781468480900
Chronic granulomatous disease (CGD) is by convention defined as a disorder involving a high susceptibility to bacterial infection related to the inability of the patient’s neutrophils to increase oxygen consumption, despite normal phagocytosis and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0eb0dee08a25ee13b56331355a0f1e2a
https://doi.org/10.1007/978-1-4684-8088-7_62
https://doi.org/10.1007/978-1-4684-8088-7_62
