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Journal Articles

Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia

Giovanna D'Andrea, Michele Schiavulli, Claudia Dimatteo, Rosa Santacroce, Egidio Guerra, Vittoria A. C. Longo, Elvira Grandone, Maurizio Margaglione

Blood (2013) 122 (26): 4289–4291.

https://doi.org/10.1182/blood-2013-09-528943

Published: 2013

Journal Articles

F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis

Samantha C. Gouw, H. Marijke van den Berg, Johannes Oldenburg, Jan Astermark, Philip G. de Groot, Maurizio Margaglione, Arthur R. Thompson, Waander van Heerde, Jorien Boekhorst, Connie H. Miller, Saskia le Cessie, Johanna G. van der Bom

Blood (2012) 119 (12): 2922–2934.

https://doi.org/10.1182/blood-2011-09-379453

Published: 2012

Includes: Supplemental data

Journal Articles

Type of Factor VIII Product as Inhibitor Risk Factor in Patients with Severe Hemophilia A and Null Mutations.

Maria Elisa Mancuso, MD, PhD, Pier Mannuccio Mannucci, MD, Angiola Rocino, MD, Isabella Garagiola, PhD, AnnaRita Tagliaferri, MD, Maurizio Margaglione, MD, Elena Santagostino, MD, PhD

Blood (2009) 114 (22): 3500.

https://doi.org/10.1182/blood.V114.22.3500.3500

Published: 2009

Journal Articles

A new JAK2 gene mutation in patients with polycythemia vera and splanchnic vein thrombosis

Donatella Colaizzo, Lucio Amitrano, Giovanni L. Tiscia, Elvira Grandone, Maria Anna Guardascione, Maurizio Margaglione

Blood (2007) 110 (7): 2768.

https://doi.org/10.1182/blood-2007-05-092502

Published: 2007

Journal Articles

The αIIbP258S, a Newly Identified Mutation, and the αIIbG349D Substitutions Cause Glanzmann Thrombasthenia by Impairing αIIb-β3 Association in the Endoplasmic Reticulum.

Andrea Artoni, MD, Federica Gelain, MBBS, Abdolreza Afrasiabi, MD, Maurizio Margaglione, MD, Pier M. Mannucci, MD

Blood (2006) 108 (11): 1098.

https://doi.org/10.1182/blood.V108.11.1098.1098

Published: 2006

Journal Articles

A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin

Giovanna D'Andrea, Rosa Lucia D'Ambrosio, Pasquale Di Perna, Massimiliano Chetta, Rosa Santacroce, Vincenzo Brancaccio, Elvira Grandone, Maurizio Margaglione

Blood (2005) 105 (2): 645–649.

https://doi.org/10.1182/blood-2004-06-2111

Published: 2005

Journal Articles

A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing

Maurizio Margaglione, Rosa Santacroce, Donatella Colaizzo, Davide Seripa, Gennaro Vecchione, Maria Rosaria Lupone, Domenico De Lucia, Paolo Fortina, Elvira Grandone, Corrado Perricone, Giovanni Di Minno

Blood (2000) 96 (7): 2501–2505.

https://doi.org/10.1182/blood.V96.7.2501

Published: 2000

NARROW

Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia

F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis

Type of Factor VIII Product as Inhibitor Risk Factor in Patients with Severe Hemophilia A and Null Mutations.

A new JAK2 gene mutation in patients with polycythemia vera and splanchnic vein thrombosis

The αIIbP258S, a Newly Identified Mutation, and the αIIbG349D Substitutions Cause Glanzmann Thrombasthenia by Impairing αIIb-β3 Association in the Endoplasmic Reticulum.

A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin

A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing

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ASH Publications

American Society of Hematology

Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia

F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis

Type of Factor VIII Product as Inhibitor Risk Factor in Patients with Severe Hemophilia A and Null Mutations.

A new JAK2 gene mutation in patients with polycythemia vera and splanchnic vein thrombosis

The αIIbP258S, a Newly Identified Mutation, and the αIIbG349D Substitutions Cause Glanzmann Thrombasthenia by Impairing αIIb-β3 Association in the Endoplasmic Reticulum.

A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin

A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing

Email alerts

ASH Publications

American Society of Hematology

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