Pierre Boisseau

Nantes, 44093, France

Last Updated: 09/26/2026

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Found 39 publications

LDLR-3'UTR Deletions Identified as a Genetic Cause of Hypobetalipoproteinemia: Evidence From Familial and Population-Based Studies.

LDLR-3'UTR Deletions Identified as a Genetic Cause of Hypobetalipoproteinemia: Evidence From Familial and Population-Based Studies.

Journal: Arteriosclerosis, thrombosis, and vascular biology

Published: June 04, 2026

Optimizing ADAMTS13 prophylaxis to reduce relapse and organ failure in congenital thrombotic thrombocytopenic purpura.

Optimizing ADAMTS13 prophylaxis to reduce relapse and organ failure in congenital thrombotic thrombocytopenic purpura.

Journal: Blood advances

Published: July 01, 2025

Optimizing ADAMTS13 prophylaxis to reduce relapse and organ failure in congenital thrombotic thrombocytopenic purpura.

Optimizing ADAMTS13 prophylaxis to reduce relapse and organ failure in congenital thrombotic thrombocytopenic purpura.

Journal: Blood advances

Published: July 01, 2025

Clinical, Phenotypic and Genotypic Characteristics of Von Willebrand Disease in Afro-Caribbeans: Results From a Study in Martinique Island, French West Indies.

Clinical, Phenotypic and Genotypic Characteristics of Von Willebrand Disease in Afro-Caribbeans: Results From a Study in Martinique Island, French West Indies.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: June 11, 2024

Genotype-Dependent Response to Desmopressin in Hemophilia A and Proposal of a Predictive Response Score.

Genotype-Dependent Response to Desmopressin in Hemophilia A and Proposal of a Predictive Response Score.

Journal: Thrombosis and haemostasis

Published: May 17, 2024

Does the VWF:CB Assay Help to Diagnose von Willebrand Factor Deficiency in Patients With a Bleeding Disorder of Unknown Cause?

Does the VWF:CB Assay Help to Diagnose von Willebrand Factor Deficiency in Patients With a Bleeding Disorder of Unknown Cause?

Journal: International journal of laboratory hematology

Published: April 27, 2024

Type 2N von Willebrand disease: genotype drives different bleeding phenotypes and treatment needs.

Type 2N von Willebrand disease: genotype drives different bleeding phenotypes and treatment needs.

Journal: Journal of thrombosis and haemostasis : JTH

Published: January 04, 2024

Management and follow-up of pregnancy-onset thrombotic thrombocytopenic purpura: the French experience.

Management and follow-up of pregnancy-onset thrombotic thrombocytopenic purpura: the French experience.

Journal: Blood advances

Published: October 19, 2023

MYH9-related disease: Assessment of the pathogenicity of a new mutation.

MYH9-related disease: Assessment of the pathogenicity of a new mutation.

Journal: EJHaem

Published: April 20, 2023

Biological, clinical features and modelling of heterozygous variants of glycoprotein Ib platelet subunit alpha (GP1BA) and glycoprotein Ib platelet subunit beta (GP1BB) genes responsible for constitutional thrombocytopenia.

Biological, clinical features and modelling of heterozygous variants of glycoprotein Ib platelet subunit alpha (GP1BA) and glycoprotein Ib platelet subunit beta (GP1BB) genes responsible for constitutional thrombocytopenia.

Journal: British journal of haematology

Published: March 04, 2022

Rare pathogenic variants in WNK3 cause X-linked intellectual disability.

Rare pathogenic variants in WNK3 cause X-linked intellectual disability.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: December 22, 2021

Identification of von Willebrand factor D4 domain mutations in patients of Afro-Caribbean descent: In vitro characterization.

Identification of von Willebrand factor D4 domain mutations in patients of Afro-Caribbean descent: In vitro characterization.

Journal: Research and practice in thrombosis and haemostasis

Published: December 02, 2021

Showing 1-12 of 39

Last Updated: 09/26/2026