Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Fretigny

Showing results (51-60 of 62) with videos related to

Pageof 7
Sort By:
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 AAmy 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 temperatureNathan 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 measurementsM 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 disabilityY 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 AAmy 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 IXCéline 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 counsellingY 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 deficiencyHamdi 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 AYohann Jourdy, Claire Bardel, Mathilde Fretigny, et al.
Hemasphere|September 15, 2021
The EHA Research Roadmap: Blood Coagulation and Hemostatic DisordersSabine Eichinger, Pierre E Morange, Marco Cattaneo, et al.
Pageof 7

Showing results (51-60 of 62) with videos related to

Sort By:
Pageof 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 AAmy 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 temperatureNathan 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 measurementsM 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 disabilityY 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 AAmy 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 IXCéline 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 counsellingY 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 deficiencyHamdi 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 AYohann Jourdy, Claire Bardel, Mathilde Fretigny, et al.
Hemasphere|September 15, 2021
The EHA Research Roadmap: Blood Coagulation and Hemostatic DisordersSabine Eichinger, Pierre E Morange, Marco Cattaneo, et al.
Pageof 7