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Haemophilia : the Official Journal of the World Federation of Hemophilia
|
July 6, 2023
Whole F8 gene sequencing combined with splicing functional analyses led to a substantial increase of the molecular diagnosis yield for non-severe haemophilia A
Amy Dericquebourg, Mathilde Fretigny, Alexandre Leuci, et al.
Soft Matter
|
October 27, 2021
Investigating the relationship between the mechanical properties of plasma polymer-like thin films and their glass transition temperature
Nathan Vinx, Pascal Damman, Philippe Leclère, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
February 13, 2014
Diagnosis and management challenges in patients with mild haemophilia A and discrepant FVIII measurements
M Trossaert, A Lienhart, C Nougier, et al.
Journal of Thrombosis and Haemostasis : JTH
|
August 2, 2016
Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability
Y Jourdy, N Chatron, M-L Carage, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
August 20, 2020
Identification of new F8 deep intronic variations in patients with haemophilia A
Amy Dericquebourg, Yohann Jourdy, Mathilde Fretigny, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
September 30, 2020
Abnormal bleeding phenotype for mild haemophilia B patients with the p.Ile112Thr variation on the gene for factor IX
Céline Row, Pierre Chamouni, Claire Berger, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 6, 2017
Molecular cytogenetic characterization of five F8 complex rearrangements: utility for haemophilia A genetic counselling
Y Jourdy, N Chatron, M Fretigny, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 20, 2024
Heterozygous large deletion mimicking homozygous substitution in MCFD2 in a patient with combined Factor V and Factor VIII deficiency
Hamdi Rezigue, Pierre Chamouni, Mathilde Fretigny, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
September 4, 2021
Complete characterisation of two new large Xq28 duplications involving F8 using whole genome sequencing in patients without haemophilia A
Yohann Jourdy, Claire Bardel, Mathilde Fretigny, et al.
Hemasphere
|
September 15, 2021
The EHA Research Roadmap: Blood Coagulation and Hemostatic Disorders
Sabine Eichinger, Pierre E Morange, Marco Cattaneo, et al.
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of 7
Search research articles
Search
Showing results (51-60 of 62) with videos related to
Sort By:
Page
of 7
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
July 6, 2023
Whole F8 gene sequencing combined with splicing functional analyses led to a substantial increase of the molecular diagnosis yield for non-severe haemophilia A
Amy Dericquebourg, Mathilde Fretigny, Alexandre Leuci, et al.
Soft Matter
|
October 27, 2021
Investigating the relationship between the mechanical properties of plasma polymer-like thin films and their glass transition temperature
Nathan Vinx, Pascal Damman, Philippe Leclère, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
February 13, 2014
Diagnosis and management challenges in patients with mild haemophilia A and discrepant FVIII measurements
M Trossaert, A Lienhart, C Nougier, et al.
Journal of Thrombosis and Haemostasis : JTH
|
August 2, 2016
Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability
Y Jourdy, N Chatron, M-L Carage, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
August 20, 2020
Identification of new F8 deep intronic variations in patients with haemophilia A
Amy Dericquebourg, Yohann Jourdy, Mathilde Fretigny, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
September 30, 2020
Abnormal bleeding phenotype for mild haemophilia B patients with the p.Ile112Thr variation on the gene for factor IX
Céline Row, Pierre Chamouni, Claire Berger, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 6, 2017
Molecular cytogenetic characterization of five F8 complex rearrangements: utility for haemophilia A genetic counselling
Y Jourdy, N Chatron, M Fretigny, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 20, 2024
Heterozygous large deletion mimicking homozygous substitution in MCFD2 in a patient with combined Factor V and Factor VIII deficiency
Hamdi Rezigue, Pierre Chamouni, Mathilde Fretigny, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
September 4, 2021
Complete characterisation of two new large Xq28 duplications involving F8 using whole genome sequencing in patients without haemophilia A
Yohann Jourdy, Claire Bardel, Mathilde Fretigny, et al.
Hemasphere
|
September 15, 2021
The EHA Research Roadmap: Blood Coagulation and Hemostatic Disorders
Sabine Eichinger, Pierre E Morange, Marco Cattaneo, et al.
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of 7