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

F G Debray

Showing results (1-10 of 15) with videos related to

Pageof 2
Sort By:
Molecular Genetics and Metabolism|June 24, 2025
The origin of abnormal organic acids in HMG-CoA synthase deficiencyF-G Debray, E Van Schaftingen
Revue Medicale De Liege|January 11, 2020
[A somatic disease causing a child psychiatric disorder]C Barrea, F G Debray, M Simon, et al.
Revue Medicale De Liege|August 11, 2017
[Progressive muscular weakness of lower limbs revealing a limb girdle muscular dystrophy]G Saintmard, G Brands, F-G Debray, et al.
Revue Medicale De Liege|October 11, 2021
[How I explore… autism spectrum disorder in a child]C Barrea, A Jadot, F G Debray, et al.
Revue Medicale De Liege|October 8, 2020
[How I explore… a disorder of intellectual development in a child]C Barrea, P Leroy, F G Debray, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 8, 2005
[A particular hereditary anemia in a two-month-old infant: elliptocytosis]F G Debray, S Ilunga, B Brichard, et al.
Revue Medicale De Liege|June 5, 2020
[Current and new therapeutic options in inborn errors of metabolism]F G Debray, L Weekers, C Dadoumont, et al.
Revue Medicale De Liege|March 26, 2009
[Osteogenesis imperfecta]J F Kaux, C Le Goff, F G Debray, et al.
Revue Medicale De Liege|December 31, 2010
[How to explore ... congenital isolated hypogonadotrophic hypogonadism]H Valdes-Socin, F G Debray, A S Parent, et al.
Neuropediatrics|May 28, 2008
Pyruvate dehydrogenase deficiency presenting as intermittent isolated acute ataxiaF-G Debray, M Lambert, R Gagne, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Molecular Genetics and Metabolism|June 24, 2025
The origin of abnormal organic acids in HMG-CoA synthase deficiencyF-G Debray, E Van Schaftingen
Revue Medicale De Liege|January 11, 2020
[A somatic disease causing a child psychiatric disorder]C Barrea, F G Debray, M Simon, et al.
Revue Medicale De Liege|August 11, 2017
[Progressive muscular weakness of lower limbs revealing a limb girdle muscular dystrophy]G Saintmard, G Brands, F-G Debray, et al.
Revue Medicale De Liege|October 11, 2021
[How I explore… autism spectrum disorder in a child]C Barrea, A Jadot, F G Debray, et al.
Revue Medicale De Liege|October 8, 2020
[How I explore… a disorder of intellectual development in a child]C Barrea, P Leroy, F G Debray, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 8, 2005
[A particular hereditary anemia in a two-month-old infant: elliptocytosis]F G Debray, S Ilunga, B Brichard, et al.
Revue Medicale De Liege|June 5, 2020
[Current and new therapeutic options in inborn errors of metabolism]F G Debray, L Weekers, C Dadoumont, et al.
Revue Medicale De Liege|March 26, 2009
[Osteogenesis imperfecta]J F Kaux, C Le Goff, F G Debray, et al.
Revue Medicale De Liege|December 31, 2010
[How to explore ... congenital isolated hypogonadotrophic hypogonadism]H Valdes-Socin, F G Debray, A S Parent, et al.
Neuropediatrics|May 28, 2008
Pyruvate dehydrogenase deficiency presenting as intermittent isolated acute ataxiaF-G Debray, M Lambert, R Gagne, et al.
Pageof 2