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Journal Articles

Trisomy 13, AML1 Mutations and M0 Subtype Are Remarkably Intricate Events in Acute Myeloid Leukemia (AML).

Olivier Nibourel, Christophe Roumier, Nathalie Philippe, Sabine Quief, Celine Villenet, Jean-Luc Laï, Nicole Dastugue, Isabelle Tigaud, John de Vos, Jean Soulier, Antonio Alberdi, Daniela Geromin, Eric Delabesse, Jean-Pierre Kerckaert, Claude Preudhomme

Blood (2007) 110 (11): 4250.

https://doi.org/10.1182/blood.V110.11.4250.4250

Published: 2007

Journal Articles

Molecular Characterization of Genomic Structural Alterations through CGH Arrays in Acute Myeloid Leukemia with Normal Cytogenetic Findings.

Christophe Roumier, MD, Sandrine Geffroy, PHD, Olivier Nibourel, MD, Sabine Quief, Celine Villenet, Aline Reneville, MD, Valeria Biggio, PHD, Jean-Luc Laï, PHD, Jean-Pierre Kerckaert, PHD, Claude Preudhomme, MD/PHD

Blood (2006) 108 (11): 105.

https://doi.org/10.1182/blood.V108.11.105.105

Published: 2006

Journal Articles

Expression of HMGA2 in PB Leukocytes and Purified CD34+ Cells from Normal Individuals and Patients with Myelofibrosis and Myeloid Metaplasia.

Joris R. Andrieux, MD, PhD, Chrystèle Bilhou-Nabera, MD, Jean Loup Demory, MD, Olivier Pierre-Louis, Brigitte Dupriez, MD, Nathalie Grardel, MD, Agnès Charpentier, MD, Vincent Praloran, MD, Francis Bauters, MD, Jean Luc Laï, PhD, Marie-Caroline Le Bousse-Kerdilès, PhD

Blood (2004) 104 (11): 2435.

https://doi.org/10.1182/blood.V104.11.2435.2435

Published: 2004

Journal Articles

HMGA2 Dysregulation in Myelofibrosis with Myeloïd Metaplasia (MMM) Versus Other Phi-Negative Chronic Myeloproliferative Disorders and Myelodysplasia.

Chrystèle Bilhou-Nabera, MD, PhD, Joris R. Andrieux, MD, PhD, Olivier Pierre-Louis, Marie-Caroline Le Bousse-Kerdilès, PhD, Brigitte Dupriez, MD, Nathalie Grardel, MD, Agnès Charpentier, MD, Vincent Praloran, MD, Francis Bauters, MD, Jean Luc Laï, PhD, Jean Loup Demory, MD

Blood (2004) 104 (11): 2436.

https://doi.org/10.1182/blood.V104.11.2436.2436

Published: 2004

Journal Articles

A report from the LALA-94 and LALA-SA groups on hypodiploidy with 30 to 39 chromosomes and near-triploidy: 2 possible expressions of a sole entity conferring poor prognosis in adult acute lymphoblastic leukemia (ALL)

Christiane Charrin, Xavier Thomas, Martine Ffrench, Quoc-Hung Le, Joris Andrieux, Marie-Joelle Mozziconacci, Jean-Luc Laï, Chrystele Bilhou-Nabera, Lucienne Michaux, Alain Bernheim, Christian Bastard, Hossein Mossafa, Christine Perot, Odile Maarek, Claude Boucheix, Véronique Lheritier, André Delannoy, Denis Fière, Nicole Dastugue

Blood (2004) 104 (8): 2444–2451.

https://doi.org/10.1182/blood-2003-04-1299

Published: 2004

Journal Articles

Several types of mutations of the Abl gene can be found in chronic myeloid leukemia patients resistant to STI571, and they can pre-exist to the onset of treatment

Catherine Roche-Lestienne, Valerie Soenen-Cornu, Nathalie Grardel-Duflos, Jean-Luc Laı̈, Nathalie Philippe, Thierry Facon, Pierre Fenaux, Claude Preudhomme

Blood (2002) 100 (3): 1014–1018.

https://doi.org/10.1182/blood.V100.3.1014

Published: 2002

Journal Articles

p16 INK4a immunocytochemical analysis is an independent prognostic factor in childhood acute lymphoblastic leukemia

Jean Hughes Dalle, Martine Fournier, Brigitte Nelken, Françoise Mazingue, Jean-Luc Laı̈, Francis Bauters, Pierre Fenaux, Bruno Quesnel

Blood (2002) 99 (7): 2620–2623.

https://doi.org/10.1182/blood.V99.7.2620

Published: 2002

Journal Articles

Chromosome 13 abnormalities identified by FISH analysis and serum β 2 -microglobulin produce a powerful myeloma staging system for patients receiving high-dose therapy

Thierry Facon, Hervé Avet-Loiseau, Gaëlle Guillerm, Philippe Moreau, Franck Geneviève, Marc Zandecki, Jean-Luc Laı̈, Xavier Leleu, Jean-Pierre Jouet, Francis Bauters, Jean-Luc Harousseau, Régis Bataille, Jean-Yves Mary

Blood (2001) 97 (6): 1566–1571.

https://doi.org/10.1182/blood.V97.6.1566

Published: 2001

Journal Articles

17p Deletion in Acute Myeloid Leukemia and Myelodysplastic Syndrome. Analysis of Breakpoints and Deleted Segments by Fluorescence In Situ

Valérie Soenen, Claude Preudhomme, Christophe Roumier, Agnès Daudignon, Jean Luc Laı̈, Pierre Fenaux

Blood (1998) 91 (3): 1008–1015.

https://doi.org/10.1182/blood.V91.3.1008

Published: 1998

Journal Articles

Acute Myeloid Leukemia and Myelodysplastic Syndromes Following Essential Thrombocythemia Treated With Hydroxyurea: High Proportion of Cases With 17p Deletion

Yvon Sterkers, Claude Preudhomme, Jean-Luc Laı̈, Jean-Loup Demory, Marie-Thérèse Caulier, Eric Wattel, Dominique Bordessoule, Francis Bauters, Pierre Fenaux

Blood (1998) 91 (2): 616–622.

https://doi.org/10.1182/blood.V91.2.616

Published: 1998

Journal Articles

Several Cytogenetic Subclones May Be Identified Within Plasma Cells From Patients With Monoclonal Gammopathy of Undetermined Significance, Both at Diagnosis and During the Indolent Course of This Condition

Marc Zandecki, Jean-Luc Laı̈, Franck Geneviève, Franck Bernardi, Hélène Volle-Rémy, Odile Blanchet, Michel François, Alain Cosson, Francis Bauters, Thierry Facon

Blood (1997) 90 (9): 3682–3690.

https://doi.org/10.1182/blood.V90.9.3682

Published: 1997

NARROW

Trisomy 13, AML1 Mutations and M0 Subtype Are Remarkably Intricate Events in Acute Myeloid Leukemia (AML).

Molecular Characterization of Genomic Structural Alterations through CGH Arrays in Acute Myeloid Leukemia with Normal Cytogenetic Findings.

Expression of HMGA2 in PB Leukocytes and Purified CD34+ Cells from Normal Individuals and Patients with Myelofibrosis and Myeloid Metaplasia.

HMGA2 Dysregulation in Myelofibrosis with Myeloïd Metaplasia (MMM) Versus Other Phi-Negative Chronic Myeloproliferative Disorders and Myelodysplasia.

A report from the LALA-94 and LALA-SA groups on hypodiploidy with 30 to 39 chromosomes and near-triploidy: 2 possible expressions of a sole entity conferring poor prognosis in adult acute lymphoblastic leukemia (ALL)

Several types of mutations of the Abl gene can be found in chronic myeloid leukemia patients resistant to STI571, and they can pre-exist to the onset of treatment

p16 INK4a immunocytochemical analysis is an independent prognostic factor in childhood acute lymphoblastic leukemia

Chromosome 13 abnormalities identified by FISH analysis and serum β 2 -microglobulin produce a powerful myeloma staging system for patients receiving high-dose therapy

17p Deletion in Acute Myeloid Leukemia and Myelodysplastic Syndrome. Analysis of Breakpoints and Deleted Segments by Fluorescence In Situ

Acute Myeloid Leukemia and Myelodysplastic Syndromes Following Essential Thrombocythemia Treated With Hydroxyurea: High Proportion of Cases With 17p Deletion

Several Cytogenetic Subclones May Be Identified Within Plasma Cells From Patients With Monoclonal Gammopathy of Undetermined Significance, Both at Diagnosis and During the Indolent Course of This Condition

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American Society of Hematology

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ASH Publications

American Society of Hematology

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