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International Journal of Laboratory Hematology
|
July 3, 2020
Pitfalls in CALR exon 9 mutation detection: A single-center experience in 571 positive patients
Emmanuelle Verger, Nabih Maslah, Marie-Helene Schlageter, et al.
Critical Reviews in Oncology/Hematology
|
November 4, 2022
Anemia in myelofibrosis: Current and emerging treatment options
Francesco Passamonti, Claire N Harrison, Ruben A Mesa, et al.
Clinical Drug Investigation
|
November 28, 2012
Efficacy and safety of cytoreductive therapies in patients with essential thrombocythaemia aged >80 years: an interim analysis of the EXELS study
Jean-Jacques Kiladjian, Carlos Besses, Martin Griesshammer, et al.
Blood Cancer Journal
|
July 28, 2021
Efficacy and tolerability of Janus kinase inhibitors in myelofibrosis: a systematic review and network meta-analysis
Léa Sureau, Corentin Orvain, Jean-Christophe Ianotto, et al.
Blood Advances
|
January 14, 2022
Single-cell analysis reveals selection of TP53-mutated clones after MDM2 inhibition
Nabih Maslah, Emmanuelle Verger, Stéphane Giraudier, et al.
Cancer
|
February 25, 2023
Early intervention in myelofibrosis and impact on outcomes: A pooled analysis of the COMFORT-I and COMFORT-II studies
Srdan Verstovsek, Jean-Jacques Kiladjian, Alessandro M Vannucchi, et al.
Ejhaem
|
August 21, 2023
Advances in management of primary myelofibrosis and polycythaemia vera: Implications in clinical practice
Shanti Amé, Fiorenza Barraco, Jean-Christophe Ianotto, et al.
Leukemia Research
|
December 4, 2012
Cytoreductive treatment patterns for essential thrombocythemia in Europe. Analysis of 3643 patients in the EXELS study
Carlos Besses, Jean-Jacques Kiladjian, Martin Griesshammer, et al.
Annals of Hematology
|
September 28, 2018
Next-generation sequencing for JAK2 mutation testing: advantages and pitfalls
Nabih Maslah, Emmanuelle Verger, Marie-Helene Schlageter, et al.
Experimental Hematology
|
February 16, 2011
Identification of JAK2 mutations in canine primary polycythemia
Stephanie Beurlet, Patricia Krief, Arnaud Sansonetti, et al.
Page
of 21
Search research articles
Search
Showing results (31-40 of 209) with videos related to
Sort By:
Page
of 21
International Journal of Laboratory Hematology
|
July 3, 2020
Pitfalls in CALR exon 9 mutation detection: A single-center experience in 571 positive patients
Emmanuelle Verger, Nabih Maslah, Marie-Helene Schlageter, et al.
Critical Reviews in Oncology/Hematology
|
November 4, 2022
Anemia in myelofibrosis: Current and emerging treatment options
Francesco Passamonti, Claire N Harrison, Ruben A Mesa, et al.
Clinical Drug Investigation
|
November 28, 2012
Efficacy and safety of cytoreductive therapies in patients with essential thrombocythaemia aged >80 years: an interim analysis of the EXELS study
Jean-Jacques Kiladjian, Carlos Besses, Martin Griesshammer, et al.
Blood Cancer Journal
|
July 28, 2021
Efficacy and tolerability of Janus kinase inhibitors in myelofibrosis: a systematic review and network meta-analysis
Léa Sureau, Corentin Orvain, Jean-Christophe Ianotto, et al.
Blood Advances
|
January 14, 2022
Single-cell analysis reveals selection of TP53-mutated clones after MDM2 inhibition
Nabih Maslah, Emmanuelle Verger, Stéphane Giraudier, et al.
Cancer
|
February 25, 2023
Early intervention in myelofibrosis and impact on outcomes: A pooled analysis of the COMFORT-I and COMFORT-II studies
Srdan Verstovsek, Jean-Jacques Kiladjian, Alessandro M Vannucchi, et al.
Ejhaem
|
August 21, 2023
Advances in management of primary myelofibrosis and polycythaemia vera: Implications in clinical practice
Shanti Amé, Fiorenza Barraco, Jean-Christophe Ianotto, et al.
Leukemia Research
|
December 4, 2012
Cytoreductive treatment patterns for essential thrombocythemia in Europe. Analysis of 3643 patients in the EXELS study
Carlos Besses, Jean-Jacques Kiladjian, Martin Griesshammer, et al.
Annals of Hematology
|
September 28, 2018
Next-generation sequencing for JAK2 mutation testing: advantages and pitfalls
Nabih Maslah, Emmanuelle Verger, Marie-Helene Schlageter, et al.
Experimental Hematology
|
February 16, 2011
Identification of JAK2 mutations in canine primary polycythemia
Stephanie Beurlet, Patricia Krief, Arnaud Sansonetti, et al.
Page
of 21