Transfusion support for a patient with McLeod phenotype without chronic granulomatous disease and with antibodies to Kx and Km
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1423-0410.2007.01021.x/fullpdf
Reference21 articles.
1. Onset of expression of the components of the Kell blood group complex
2. A New Phenotype (McLeod) in the Kell Blood-group System
3. Genetic linkage between the Kell blood group system and prolactin-inducible protein loci: provisional assignment of KEL to chromosome 7
4. The human Kell blood group gene maps to chromosome 7q33 and its expression is restricted to erythroid cells
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1. The protean presentations of XK disease (McLeod syndrome): a case series with new observations and updates on previously reported families;Frontiers in Neuroscience;2024-09-09
2. How we approach transfusions in a patient with high risk of alloimmunization from McLeod phenotype;Pediatric Blood & Cancer;2022-12-10
3. Kell Blood Group System: A Systematic Review and Meta-Analysis;2022-10-10
4. A patient with McLeod syndrome showing involvement of the central sensorimotor tracts for the legs;BMC Neurology;2019-11-27
5. Unmasking of novel mutations within XK gene that could be used as Diagnostic Markers to Predict McLeod syndrome: Using in silico analysis;2019-02-05
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