Page 1 | Search Results | Blood | American Society of Hematology

1-5 of 5

Sort by

Sort Order Select

Journal Articles

Genome Wide SNP Analysis Reveals Frequent Cryptic Clonal Chromosomal Aberrations Including Uniparental Disomy (UPD) in Waldenstrom's Macroglobulinemia.

Stephanie Poulain, MD, Christophe Roumier, PhD, Meyling Cheok, PhD, Sylvie Zoutina, PhD, Agnes Daudignon, MPharm, Olivier Nibourel, MPharm, Valérie Soenen, MPharm, Jean Luc Lai, PhD, Jose Fernandez, MD, Claude Preudhomme, Patrick Duthilleul, MPharm, Pierre Morel, MD, Xavier Leleu

Blood (2009) 114 (22): 3932.

https://doi.org/10.1182/blood.V114.22.3932.3932

Published: 2009

Journal Articles

RUNX1 DNA-Binding Mutations and RUNX1-PRDM16 Cryptic Fusion in BCR/ABL+ Leukemias Are Frequently Associated with Secondary Trisomy 21 and May Contribute to Clonal Evolution and Imatinib Resistance.

Catherine Roche-Lestienne, PhD, Laureline Deluche, MD, Selim Corm, MD, Isabelle Tigaud, MD, Sami Joha, PhD, Nathalie Philippe, PhD, Sandrine Geffroy, PhD, Jean-Luc Lai, PhD, Franck Nicolini, MD, PhD, Claude Preudhomme, MD, PhD

Blood (2007) 110 (11): 2786.

https://doi.org/10.1182/blood.V110.11.2786.2786

Published: 2007

Journal Articles

A Retrospective Survey of Imatinib Mesylate Treatment for Chronic Myeloid Leukemia in a Northern France Region.

Selim Corm, MD, Ariane Leroyer, MD, Mathieu Wemeau, MD, Bruno Bregman, PhD, Abderrahim Oukessou, MD, Michiel Hemels, MD, Claude Preudhomme, MD, PhD, Jean-Pierre Jouet, MD, Jean-Luc Lai, PhD, Thierry Facon, MD

Blood (2006) 108 (11): 4800.

https://doi.org/10.1182/blood.V108.11.4800.4800

Published: 2006

Journal Articles

A Retrospective 20-Year Survey of the Incidence of Chronic Myeloid Leukemia in the Northern France Region.

Selim Corm, MD, Ariane Leroyer, MD, Mathieu Wemeau, MD, Bruno Bregman, PhD, Abderrahim Oukessou, MD, Claude Preudhomme, MD, PhD, Jean-Pierre Jouet, MD, Jean-Luc Lai, PhD, Thierry Facon, MD

Blood (2006) 108 (11): 4798.

https://doi.org/10.1182/blood.V108.11.4798.4798

Published: 2006

Journal Articles

Molecular Characterization of the Idiopathic Hypereosinophilic Syndrome (HES) in 35 French Patients with Normal Conventional Cytogenetics.

Catherine Roche-Lestienne, PhD, Valerie Soenen-Cornu, MD, PhD, Jean-Emmanuel Kahn, MD, Jean-Luc Lai, PhD, Eric Hachulla, MD, Francois Drupt, MD, Anne-Laure Demarty, MD, Martine Gardembas, MD, Nathalie Philippe, Stephane Barette, MD, Christian Libersa, MD, PhD, Olivier Bletry, MD, PhD, Christian Rose, MD, PhD, Pierre Fenaux, MD, PhD, Lionel Prin, MD, PhD, Claude Preudhomme, MD, PhD

Blood (2004) 104 (11): 2442.

https://doi.org/10.1182/blood.V104.11.2442.2442

Published: 2004

NARROW

Genome Wide SNP Analysis Reveals Frequent Cryptic Clonal Chromosomal Aberrations Including Uniparental Disomy (UPD) in Waldenstrom's Macroglobulinemia.

RUNX1 DNA-Binding Mutations and RUNX1-PRDM16 Cryptic Fusion in BCR/ABL+ Leukemias Are Frequently Associated with Secondary Trisomy 21 and May Contribute to Clonal Evolution and Imatinib Resistance.

A Retrospective Survey of Imatinib Mesylate Treatment for Chronic Myeloid Leukemia in a Northern France Region.

A Retrospective 20-Year Survey of the Incidence of Chronic Myeloid Leukemia in the Northern France Region.

Molecular Characterization of the Idiopathic Hypereosinophilic Syndrome (HES) in 35 French Patients with Normal Conventional Cytogenetics.

Email alerts

ASH Publications

American Society of Hematology

Genome Wide SNP Analysis Reveals Frequent Cryptic Clonal Chromosomal Aberrations Including Uniparental Disomy (UPD) in Waldenstrom's Macroglobulinemia.

RUNX1 DNA-Binding Mutations and RUNX1-PRDM16 Cryptic Fusion in BCR/ABL+ Leukemias Are Frequently Associated with Secondary Trisomy 21 and May Contribute to Clonal Evolution and Imatinib Resistance.

A Retrospective Survey of Imatinib Mesylate Treatment for Chronic Myeloid Leukemia in a Northern France Region.

A Retrospective 20-Year Survey of the Incidence of Chronic Myeloid Leukemia in the Northern France Region.

Molecular Characterization of the Idiopathic Hypereosinophilic Syndrome (HES) in 35 French Patients with Normal Conventional Cytogenetics.

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only