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P Hillmen

Showing results (11-20 of 52) with videos related to

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British Journal of Haematology|August 1, 1994
Mutations in the PIG-A gene causing partial deficiency of GPI-linked surface proteins (PNH II) in patients with paroxysmal nocturnal haemoglobinuriaM Bessler, P J Mason, P Hillmen, et al.
Blood|January 1, 1993
Production and characterization of lymphoblastoid cell lines with the paroxysmal nocturnal hemoglobinuria phenotypeP Hillmen, M Bessler, D H Crawford, et al.
Haematologica|April 5, 2007
Erythopoietin treatment during complement inhibition with eculizumab in a patient with paroxysmal nocturnal hemoglobinuriaA Hill, S J Richards, R P Rother, et al.
Leukemia|October 20, 2006
Flow cytometric protein expression profiling as a systematic approach for developing disease-specific assays: identification of a chronic lymphocytic leukaemia-specific assay for use in rituximab-containing regimensA C Rawstron, R de Tute, A S Jack, et al.
Blood|August 26, 1998
Lymphocyte subset analysis and glycosylphosphatidylinositol phenotype in patients with paroxysmal nocturnal hemoglobinuriaS J Richards, D R Norfolk, D M Swirsky, 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.
Blood|December 15, 1995
Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift typeK Nafa, P J Mason, P Hillmen, et al.
Human Molecular Genetics|May 1, 1994
Genomic organization of the X-linked gene (PIG-A) that is mutated in paroxysmal nocturnal haemoglobinuria and of a related autosomal pseudogene mapped to 12q21M Bessler, P Hillmen, L Longo, et al.
The New England Journal of Medicine|November 9, 1995
Natural history of paroxysmal nocturnal hemoglobinuriaP Hillmen, S M Lewis, M Bessler, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1993
Specific defect in N-acetylglucosamine incorporation in the biosynthesis of the glycosylphosphatidylinositol anchor in cloned cell lines from patients with paroxysmal nocturnal hemoglobinuriaP Hillmen, M Bessler, P J Mason, et al.
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
British Journal of Haematology|August 1, 1994
Mutations in the PIG-A gene causing partial deficiency of GPI-linked surface proteins (PNH II) in patients with paroxysmal nocturnal haemoglobinuriaM Bessler, P J Mason, P Hillmen, et al.
Blood|January 1, 1993
Production and characterization of lymphoblastoid cell lines with the paroxysmal nocturnal hemoglobinuria phenotypeP Hillmen, M Bessler, D H Crawford, et al.
Haematologica|April 5, 2007
Erythopoietin treatment during complement inhibition with eculizumab in a patient with paroxysmal nocturnal hemoglobinuriaA Hill, S J Richards, R P Rother, et al.
Leukemia|October 20, 2006
Flow cytometric protein expression profiling as a systematic approach for developing disease-specific assays: identification of a chronic lymphocytic leukaemia-specific assay for use in rituximab-containing regimensA C Rawstron, R de Tute, A S Jack, et al.
Blood|August 26, 1998
Lymphocyte subset analysis and glycosylphosphatidylinositol phenotype in patients with paroxysmal nocturnal hemoglobinuriaS J Richards, D R Norfolk, D M Swirsky, 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.
Blood|December 15, 1995
Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift typeK Nafa, P J Mason, P Hillmen, et al.
Human Molecular Genetics|May 1, 1994
Genomic organization of the X-linked gene (PIG-A) that is mutated in paroxysmal nocturnal haemoglobinuria and of a related autosomal pseudogene mapped to 12q21M Bessler, P Hillmen, L Longo, et al.
The New England Journal of Medicine|November 9, 1995
Natural history of paroxysmal nocturnal hemoglobinuriaP Hillmen, S M Lewis, M Bessler, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1993
Specific defect in N-acetylglucosamine incorporation in the biosynthesis of the glycosylphosphatidylinositol anchor in cloned cell lines from patients with paroxysmal nocturnal hemoglobinuriaP Hillmen, M Bessler, P J Mason, et al.
Pageof 6