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Blood
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April 15, 1997
Both paroxysmal nocturnal hemoglobinuria (PNH) type II cells and PNH type III cells can arise from different point mutations involving the same codon of the PIG-A gene
S Rollinson, S Richards, D Norfolk, et al.
British Journal of Haematology
|
March 1, 1991
Primary thrombocythaemia in pregnancy
J Beard, P Hillmen, C C Anderson, et al.
British Journal of Haematology
|
March 1, 1996
Serum erythropoietin levels in paroxysmal nocturnal haemoglobinuria: implications for therapy
M F McMullin, P Hillmen, G E Elder, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
September 25, 2016
appendix 6: Chronic lymphocytic leukaemia: eUpdate published online September 2016 (http://www.esmo.org/Guidelines/Haematological-Malignancies)
B Eichhorst, T Robak, E Montserrat, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
August 29, 2015
Chronic lymphocytic leukaemia: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up
B Eichhorst, T Robak, E Montserrat, et al.
Haematologica
|
November 1, 1996
Factor V Leiden mutation investigated by amplification created restriction enzyme site (ACRES) in PNH patients with and without thrombosis
K Nafa, M Bessler, P Mason, et al.
Leukemia
|
January 27, 2006
Monoclonal B-cell lymphocytosis (MBL) in CLL families: substantial increase in relative risk for young adults
R de Tute, M Yuille, D Catovsky, et al.
Leukemia Research
|
December 15, 2010
Eculizumab for patients with paroxysmal nocturnal hemoglobinuria (PNH) is effective during the maintenance of hemodialysis for end stage renal failure
R J Kelly, A Hill, L M Arnold, et al.
British Journal of Haematology
|
April 17, 2004
Guidelines on the diagnosis and management of chronic lymphocytic leukaemia
D Oscier, C Fegan, P Hillmen, et al.
The EMBO Journal
|
January 1, 1994
Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene
M Bessler, P J Mason, P Hillmen, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 52) with videos related to
Sort By:
Page
of 6
Blood
|
April 15, 1997
Both paroxysmal nocturnal hemoglobinuria (PNH) type II cells and PNH type III cells can arise from different point mutations involving the same codon of the PIG-A gene
S Rollinson, S Richards, D Norfolk, et al.
British Journal of Haematology
|
March 1, 1991
Primary thrombocythaemia in pregnancy
J Beard, P Hillmen, C C Anderson, et al.
British Journal of Haematology
|
March 1, 1996
Serum erythropoietin levels in paroxysmal nocturnal haemoglobinuria: implications for therapy
M F McMullin, P Hillmen, G E Elder, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
September 25, 2016
appendix 6: Chronic lymphocytic leukaemia: eUpdate published online September 2016 (http://www.esmo.org/Guidelines/Haematological-Malignancies)
B Eichhorst, T Robak, E Montserrat, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
August 29, 2015
Chronic lymphocytic leukaemia: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up
B Eichhorst, T Robak, E Montserrat, et al.
Haematologica
|
November 1, 1996
Factor V Leiden mutation investigated by amplification created restriction enzyme site (ACRES) in PNH patients with and without thrombosis
K Nafa, M Bessler, P Mason, et al.
Leukemia
|
January 27, 2006
Monoclonal B-cell lymphocytosis (MBL) in CLL families: substantial increase in relative risk for young adults
R de Tute, M Yuille, D Catovsky, et al.
Leukemia Research
|
December 15, 2010
Eculizumab for patients with paroxysmal nocturnal hemoglobinuria (PNH) is effective during the maintenance of hemodialysis for end stage renal failure
R J Kelly, A Hill, L M Arnold, et al.
British Journal of Haematology
|
April 17, 2004
Guidelines on the diagnosis and management of chronic lymphocytic leukaemia
D Oscier, C Fegan, P Hillmen, et al.
The EMBO Journal
|
January 1, 1994
Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene
M Bessler, P J Mason, P Hillmen, et al.
Page
of 6