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P Hillmen

Showing results (21-30 of 52) with videos related to

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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 geneS Rollinson, S Richards, D Norfolk, et al.
British Journal of Haematology|March 1, 1991
Primary thrombocythaemia in pregnancyJ Beard, P Hillmen, C C Anderson, 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.
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-upB 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 thrombosisK 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 adultsR 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 failureR 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 leukaemiaD 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 geneM Bessler, P J Mason, P Hillmen, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 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 geneS Rollinson, S Richards, D Norfolk, et al.
British Journal of Haematology|March 1, 1991
Primary thrombocythaemia in pregnancyJ Beard, P Hillmen, C C Anderson, 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.
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-upB 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 thrombosisK 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 adultsR 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 failureR 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 leukaemiaD 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 geneM Bessler, P J Mason, P Hillmen, et al.
Pageof 6