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T Reilly

Showing results (581-590 of 605) with videos related to

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The New England Journal of Medicine|July 8, 2005
Hydroxyurea compared with anagrelide in high-risk essential thrombocythemiaClaire N Harrison, Peter J Campbell, Georgina Buck, et al.
Blood|May 3, 2008
MPL mutations in myeloproliferative disorders: analysis of the PT-1 cohortPhilip A Beer, Peter J Campbell, Linda M Scott, et al.
Scientific Reports|August 31, 2017
Atp6ap2 ablation in adult mice impairs viability through multiple organ deficienciesOlivia Wendling, Marie-France Champy, Solène Jaubert, et al.
Leukemia|August 31, 2007
Proposed criteria for the diagnosis of post-polycythemia vera and post-essential thrombocythemia myelofibrosis: a consensus statement from the International Working Group for Myelofibrosis Research and TreatmentG Barosi, R A Mesa, J Thiele, et al.
Haematologica|December 5, 2015
STAT1 activation in association with JAK2 exon 12 mutationsAnna L Godfrey, Edwin Chen, Charles E Massie, et al.
British Journal of Haematology|August 23, 2014
Monitoring of chimerism following allogeneic haematopoietic stem cell transplantation (HSCT): technical recommendations for the use of short tandem repeat (STR) based techniques, on behalf of the United Kingdom National External Quality Assessment Service for Leucocyte Immunophenotyping Chimerism Working GroupJordan R Clark, Stuart D Scott, Andrea L Jack, et al.
British Journal of Haematology|June 2, 2012
Guideline for the diagnosis and management of myelofibrosisJohn T Reilly, Mary Frances McMullin, Philip A Beer, et al.
Blood|May 10, 2007
Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: recommendations from an ad hoc international expert panelAyalew Tefferi, Juergen Thiele, Attilio Orazi, et al.
Blood|August 18, 2012
JAK2V617F homozygosity arises commonly and recurrently in PV and ET, but PV is characterized by expansion of a dominant homozygous subcloneAnna L Godfrey, Edwin Chen, Francesca Pagano, et al.
British Journal of Haematology|March 25, 2010
Guideline for investigation and management of adults and children presenting with a thrombocytosisClaire N Harrison, David Bareford, Nauman Butt, et al.
Pageof 61

Showing results (581-590 of 605) with videos related to

Sort By:
Pageof 61
The New England Journal of Medicine|July 8, 2005
Hydroxyurea compared with anagrelide in high-risk essential thrombocythemiaClaire N Harrison, Peter J Campbell, Georgina Buck, et al.
Blood|May 3, 2008
MPL mutations in myeloproliferative disorders: analysis of the PT-1 cohortPhilip A Beer, Peter J Campbell, Linda M Scott, et al.
Scientific Reports|August 31, 2017
Atp6ap2 ablation in adult mice impairs viability through multiple organ deficienciesOlivia Wendling, Marie-France Champy, Solène Jaubert, et al.
Leukemia|August 31, 2007
Proposed criteria for the diagnosis of post-polycythemia vera and post-essential thrombocythemia myelofibrosis: a consensus statement from the International Working Group for Myelofibrosis Research and TreatmentG Barosi, R A Mesa, J Thiele, et al.
Haematologica|December 5, 2015
STAT1 activation in association with JAK2 exon 12 mutationsAnna L Godfrey, Edwin Chen, Charles E Massie, et al.
British Journal of Haematology|August 23, 2014
Monitoring of chimerism following allogeneic haematopoietic stem cell transplantation (HSCT): technical recommendations for the use of short tandem repeat (STR) based techniques, on behalf of the United Kingdom National External Quality Assessment Service for Leucocyte Immunophenotyping Chimerism Working GroupJordan R Clark, Stuart D Scott, Andrea L Jack, et al.
British Journal of Haematology|June 2, 2012
Guideline for the diagnosis and management of myelofibrosisJohn T Reilly, Mary Frances McMullin, Philip A Beer, et al.
Blood|May 10, 2007
Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: recommendations from an ad hoc international expert panelAyalew Tefferi, Juergen Thiele, Attilio Orazi, et al.
Blood|August 18, 2012
JAK2V617F homozygosity arises commonly and recurrently in PV and ET, but PV is characterized by expansion of a dominant homozygous subcloneAnna L Godfrey, Edwin Chen, Francesca Pagano, et al.
British Journal of Haematology|March 25, 2010
Guideline for investigation and management of adults and children presenting with a thrombocytosisClaire N Harrison, David Bareford, Nauman Butt, et al.
Pageof 61