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

L J De Meirleir

Showing results (1-10 of 7) with videos related to

Pageof 1
Sort By:
Pediatric Neurology|January 1, 1986
Evoked potentials in comatose children: auditory brainstem responsesL J De Meirleir, M J Taylor
Pediatric Neurology|March 1, 1987
Prognostic utility of SEPs in comatose childrenL J De Meirleir, M J Taylor
Pediatric Neurology|July 3, 1998
Dancing eye syndrome and hyperphosphatasemiaD E Hasaerts, F K Gorus, L J De Meirleir
Journal of Inherited Metabolic Disease|January 1, 1991
Pyruvate dehydrogenase deficiency due to a mutation of the E1 alpha subunitL J de Meirleir, W Lissens, E Vamos, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 1, 1988
Multimodal evoked potential studies in leukodystrophies of childrenL J De Meirleir, M J Taylor, W J Logan
Pediatric Research|September 1, 1990
Impaired skin fibroblast carnitine uptake in primary systemic carnitine deficiency manifested by childhood carnitine-responsive cardiomyopathyI Tein, D C De Vivo, F Bierman, et al.
Biochemical and Biophysical Research Communications|November 9, 2005
Aminoacylase I deficiency: a novel inborn error of metabolismR N Van Coster, E A Gerlo, T G Giardina, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Pediatric Neurology|January 1, 1986
Evoked potentials in comatose children: auditory brainstem responsesL J De Meirleir, M J Taylor
Pediatric Neurology|March 1, 1987
Prognostic utility of SEPs in comatose childrenL J De Meirleir, M J Taylor
Pediatric Neurology|July 3, 1998
Dancing eye syndrome and hyperphosphatasemiaD E Hasaerts, F K Gorus, L J De Meirleir
Journal of Inherited Metabolic Disease|January 1, 1991
Pyruvate dehydrogenase deficiency due to a mutation of the E1 alpha subunitL J de Meirleir, W Lissens, E Vamos, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 1, 1988
Multimodal evoked potential studies in leukodystrophies of childrenL J De Meirleir, M J Taylor, W J Logan
Pediatric Research|September 1, 1990
Impaired skin fibroblast carnitine uptake in primary systemic carnitine deficiency manifested by childhood carnitine-responsive cardiomyopathyI Tein, D C De Vivo, F Bierman, et al.
Biochemical and Biophysical Research Communications|November 9, 2005
Aminoacylase I deficiency: a novel inborn error of metabolismR N Van Coster, E A Gerlo, T G Giardina, et al.
Pageof 1