Recent developments in the understanding and management of paroxysmal nocturnal haemoglobinuria
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2007.06554.x/fullpdf
Reference107 articles.
1. Pulmonary Thrombotic Arteriopathy in Patients With Sickle Cell Disease
2. Hypomorphic promoter mutation in PIGM causes inherited glycosylphosphatidylinositol deficiency
3. Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals
4. High incidence of thrombosis in African-American and Latin-American patients with Paroxysmal Nocturnal Haemoglobinuria
5. Affected paroxysmal nocturnal hemoglobinuria T lymphocytes harbor a common defect in assembly of N-acetyl-D-glucosamine inositol phospholipid corresponding to that in class A Thy-1- murine lymphoma mutants.
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