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Journal Articles

The Highly Prevalent Deletions in F8 Intron 13 Found in French Mild Haemophilia a Patients Result of Both Founder Effect and Recurrent De Novo Events

Yohann Jourdy, PhD PharmD, Mathilde Fretigny, PharmD, Fanny Lassalle, PharmD, David Lillicrap, MD, Claude Negrier, Patrice Bouvagnet, MD, Christine Vinciguerra, PharmD

Blood (2018) 132 (Supplement 1): 2489.

https://doi.org/10.1182/blood-2018-99-111791

Published: 2018

Journal Articles

High-Throughput Genotyping of Haemophilia A and B Using Next-Generation Sequencing Technology in Lille University Hospital

Fanny Lassalle, PharmD, Antoine Rauch, MD PhD, Benedicte Wibaut, MD PhD, Christine Vinciguerra, PharmD, PhD, Mathilde Fretigny, PharmD, PhD, Bertrand Vaast, Valerie Gomanne, Sophie Susen, MD PhD, Jenny Goudemand, MD PhD, Christophe Zawadzki, PharmD, PhD

Blood (2015) 126 (23): 2273.

https://doi.org/10.1182/blood.V126.23.2273.2273

Published: 2015

Journal Articles

Recombinant factor VIII products and inhibitor development in previously untreated boys with severe hemophilia A

Thierry Calvez, Hervé Chambost, Ségolène Claeyssens-Donadel, Roseline d’Oiron, Véronique Goulet, Benoît Guillet, Virginie Héritier, Vanessa Milien, Chantal Rothschild, Valérie Roussel-Robert, Christine Vinciguerra, Jenny Goudemand

Blood (2014) 124 (23): 3398–3408.

https://doi.org/10.1182/blood-2014-07-586347

Published: 2014

Includes: Supplemental data

Journal Articles

Description of a Large Duplication in F8 Gene Responsible for Severe Hemophilia A.

Christine Vinciguerra, Jenny Goudemand, Christophe Zawadzki, Dorothee Pellecchia, Claude Negrier

Blood (2007) 110 (11): 1149.

https://doi.org/10.1182/blood.V110.11.1149.1149

Published: 2007

Journal Articles

Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A

Sophie Valleix, Christine Vinciguerra, Jean-Maurice Lavergne, Marco Leuer, Marc Delpech, Claude Negrier

Blood (2002) 100 (8): 3034–3036.

https://doi.org/10.1182/blood-2002-01-0277

Published: 2002

Journal Articles

ERGIC-53 Gene Structure and Mutation Analysis in 19 Combined Factors V and VIII Deficiency Families

Blood (1999) 93 (7): 2261–2266.

https://doi.org/10.1182/blood.V93.7.2261

Published: 1999

NARROW

The Highly Prevalent Deletions in F8 Intron 13 Found in French Mild Haemophilia a Patients Result of Both Founder Effect and Recurrent De Novo Events

High-Throughput Genotyping of Haemophilia A and B Using Next-Generation Sequencing Technology in Lille University Hospital

Recombinant factor VIII products and inhibitor development in previously untreated boys with severe hemophilia A

Description of a Large Duplication in F8 Gene Responsible for Severe Hemophilia A.

Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A

ERGIC-53 Gene Structure and Mutation Analysis in 19 Combined Factors V and VIII Deficiency Families

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ASH Publications

American Society of Hematology

The Highly Prevalent Deletions in F8 Intron 13 Found in French Mild Haemophilia a Patients Result of Both Founder Effect and Recurrent De Novo Events

High-Throughput Genotyping of Haemophilia A and B Using Next-Generation Sequencing Technology in Lille University Hospital

Recombinant factor VIII products and inhibitor development in previously untreated boys with severe hemophilia A

Description of a Large Duplication in F8 Gene Responsible for Severe Hemophilia A.

Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A

ERGIC-53 Gene Structure and Mutation Analysis in 19 Combined Factors V and VIII Deficiency Families

Email alerts

ASH Publications

American Society of Hematology

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