Sabine-marie Castet

Bordeaux, France

Last Updated: 09/26/2026

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Found 8 publications

F8 gene variants influence the response to desmopressin in hemophilia A carriers.

F8 gene variants influence the response to desmopressin in hemophilia A carriers.

Journal: Blood

Published: May 06, 2025

Whole F8 gene sequencing combined with splicing functional analyses led to a substantial increase of the molecular diagnosis yield for non-severe haemophilia A.

Whole F8 gene sequencing combined with splicing functional analyses led to a substantial increase of the molecular diagnosis yield for non-severe haemophilia A.

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

Published: April 26, 2023

Reinvestigation of unidentified causative variants in FXI-deficient patients: Focus on gene segment deletions.

Reinvestigation of unidentified causative variants in FXI-deficient patients: Focus on gene segment deletions.

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

Published: April 29, 2022

Global Seroprevalence of Pre-existing Immunity Against AAV5 and Other AAV Serotypes in People with Hemophilia A.

Global Seroprevalence of Pre-existing Immunity Against AAV5 and Other AAV Serotypes in People with Hemophilia A.

Journal: Human gene therapy

Published: February 14, 2022

Atypical late diagnosis of Noonan syndrome revealed by bleedings due to platelet dysfunction.

Atypical late diagnosis of Noonan syndrome revealed by bleedings due to platelet dysfunction.

Journal: Journal of thrombosis and thrombolysis

Published: July 25, 2021

Evaluation of the potential utility of the total thrombus-formation analysis system in comparison to the platelet function analyser in subjects with primary haemostatic defects.

Evaluation of the potential utility of the total thrombus-formation analysis system in comparison to the platelet function analyser in subjects with primary haemostatic defects.

Journal: British journal of haematology

Published: July 02, 2020

Gastrointestinal bleeding from angiodysplasia in von Willebrand disease: Improved diagnosis and outcome prediction using videocapsule on top of conventional endoscopy.

Gastrointestinal bleeding from angiodysplasia in von Willebrand disease: Improved diagnosis and outcome prediction using videocapsule on top of conventional endoscopy.

Journal: Journal of thrombosis and haemostasis : JTH

Published: June 03, 2020

Severe hemophilia A caused by an unbalanced chromosomal rearrangement identified using nanopore sequencing.

Severe hemophilia A caused by an unbalanced chromosomal rearrangement identified using nanopore sequencing.

Journal: Journal of thrombosis and haemostasis : JTH

Published: March 14, 2019

Showing 1-8 of 8

Last Updated: 09/26/2026