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Current Opinion in Hematology|March 1, 1996
The dual pathogenesis of paroxysmal nocturnal hemoglobinuriaL Luzzatto, M BesslerThe EMBO Journal|January 1, 1994
Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A geneM Bessler, P J Mason, P Hillmen, et al.British Journal of Haematology|March 1, 1992
Two distinct patterns of glycosylphosphatidylinositol (GPI) linked protein deficiency in the red cells of patients with paroxysmal nocturnal haemoglobinuriaP Hillmen, J M Hows, L LuzzattoTrends in Genetics : TIG|April 1, 1992
The molecular basis of glucose-6-phosphate dehydrogenase deficiencyT Vulliamy, P Mason, L LuzzattoBlood|October 27, 1998
New somatic mutation in the PIG-A gene emerges at relapse of paroxysmal nocturnal hemoglobinuriaK Nafa, M Bessler, H J Deeg, et al.Journal of Internal Medicine|January 1, 1994
Tissue plasminogen activator for hepatic vein thrombosis in paroxysmal nocturnal haemoglobinuriaM F McMullin, P Hillmen, J Jackson, et al.British Journal of Haematology|June 1, 1994
Myelodysplasia in a patient with pre-existing paroxysmal nocturnal haemoglobinuria: a clonal disease originating from within a clonal diseaseL Longo, M Bessler, P Beris, et al.Blood Cells, Molecules & Diseases|October 29, 1998
The spectrum of somatic mutations in the PIG-A gene in paroxysmal nocturnal hemoglobinuria includes large deletions and small duplicationsK Nafa, M Bessler, H Castro-Malaspina, et al.British Journal of Haematology|March 1, 1996
Serum erythropoietin levels in paroxysmal nocturnal haemoglobinuria: implications for therapyM F McMullin, P Hillmen, G E Elder, et al.The Journal of Clinical Investigation|September 1, 1997
Murine embryonic stem cells without pig-a gene activity are competent for hematopoiesis with the PNH phenotype but not for clonal expansionV Rosti, G Tremml, V Soares, et al.Pageof 162