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Journal Articles

Compound Heterozygosity of a W493C Substitution and R704/Premature Stop Codon within the γ-Glutamyl Carboxylase in Combined Vitamin K-Dependent Coagulation Factor Deficiency in a French Family.

Dhouha Darghouth, PhD, Kevin W Hallgren, Odile Issertial, Amine Bazaa, PhD, Kathleen L Berkner, PhD, Jean-Philippe Rosa, MD, PhD, Rémi Favier, MD

Blood (2009) 114 (22): 1302.

https://doi.org/10.1182/blood.V114.22.1302.1302

Published: 2009

Journal Articles

In Vitro Knock-Down of Myh9 Leads to a Myh9-Related Disorder Phenotype in Human Megakaryocytes.

Yolande Chen, MD, Siham Boukour, PhD, Monia Romdhane, Ababacar Seye, PhD, Olivier Bluteau, PhD, Larissa Lordier, PhD, Yunhua Chang, PhD, Anne Galy, D., Pharm, and, PhD, Rémi Favier, MD, Paquita Nurden, MD, Hana Raslova, PhD, William Vainchenker, MD, PhD, Najet Debili, PhD

Blood (2009) 114 (22): 4596.

https://doi.org/10.1182/blood.V114.22.4596.4596

Published: 2009

Journal Articles

Newly recognized cellular abnormalities in the gray platelet syndrome

Arnaud Drouin, Rémi Favier, Jean-Marc Massé, Najet Debili, Alain Schmitt, Carole Elbim, Josette Guichard, Mircea Adam, Marie-Anne Gougerot-Pocidalo, Elisabeth M. Cramer

Blood (2001) 98 (5): 1382–1391.

https://doi.org/10.1182/blood.V98.5.1382

Published: 2001

Journal Articles

Unbalanced X-chromosome inactivation with a novel FVIII gene mutation resulting in severe hemophilia A in a female

Rémi Favier, Jean-Maurice Lavergne, Jean-Marc Costa, Claudine Caron, Claudine Mazurier, Michèle Viémont, Marc Delpech, Sophie Valleix

Blood (2000) 96 (13): 4373–4375.

https://doi.org/10.1182/blood.V96.13.4373

Published: 2000

Journal Articles

Existence of a differentiation blockage at the stage of a megakaryocyte precursor in the thrombocytopenia and absent radii (TAR) syndrome

Rémi Letestu, Natacha Vitrat, Aline Massé, Jean-Pierre Le Couedic, Vladimir Lazar, Philippe Rameau, Françoise Wendling, Jacqueline Vuillier, Patrick Boutard, Emmanuel Plouvier, Mireille Plasse, Rémi Favier, William Vainchenker, Najet Debili

Blood (2000) 95 (5): 1633–1641.

https://doi.org/10.1182/blood.V95.5.1633.005k25_1633_1641

Published: 2000

NARROW

Compound Heterozygosity of a W493C Substitution and R704/Premature Stop Codon within the γ-Glutamyl Carboxylase in Combined Vitamin K-Dependent Coagulation Factor Deficiency in a French Family.

In Vitro Knock-Down of Myh9 Leads to a Myh9-Related Disorder Phenotype in Human Megakaryocytes.

Newly recognized cellular abnormalities in the gray platelet syndrome

Unbalanced X-chromosome inactivation with a novel FVIII gene mutation resulting in severe hemophilia A in a female

Existence of a differentiation blockage at the stage of a megakaryocyte precursor in the thrombocytopenia and absent radii (TAR) syndrome

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ASH Publications

American Society of Hematology

Compound Heterozygosity of a W493C Substitution and R704/Premature Stop Codon within the γ-Glutamyl Carboxylase in Combined Vitamin K-Dependent Coagulation Factor Deficiency in a French Family.

In Vitro Knock-Down of Myh9 Leads to a Myh9-Related Disorder Phenotype in Human Megakaryocytes.

Newly recognized cellular abnormalities in the gray platelet syndrome

Unbalanced X-chromosome inactivation with a novel FVIII gene mutation resulting in severe hemophilia A in a female

Existence of a differentiation blockage at the stage of a megakaryocyte precursor in the thrombocytopenia and absent radii (TAR) syndrome

Email alerts

ASH Publications

American Society of Hematology

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