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

V Valayannopoulos

Showing results (31-40 of 35) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 35 results.
Journal of Neuroradiology = Journal De Neuroradiologie|April 10, 2010
Posterior fossa imaging in 158 children with ataxiaN Boddaert, I Desguerre, N Bahi-Buisson, et al.
Neurology|July 7, 2010
Mitochondrial ND5 mutations mimicking brainstem tectal gliomaM Rio, A S Lebre, P de Lonlay, et al.
Molecular Genetics and Metabolism|June 12, 2013
Renal transplantation in 4 patients with methylmalonic aciduria: a cell therapy for metabolic diseaseA Brassier, O Boyer, V Valayannopoulos, et al.
Journal of Medical Genetics|October 26, 2010
A common pattern of brain MRI imaging in mitochondrial diseases with complex I deficiencyA S Lebre, M Rio, L Faivre d'Arcier, et al.
Journal of Medical Genetics|May 7, 2013
Phenotype and genotype in 101 males with X-linked creatine transporter deficiencyJ M van de Kamp, O T Betsalel, S Mercimek-Mahmutoglu, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Journal of Neuroradiology = Journal De Neuroradiologie|April 10, 2010
Posterior fossa imaging in 158 children with ataxiaN Boddaert, I Desguerre, N Bahi-Buisson, et al.
Neurology|July 7, 2010
Mitochondrial ND5 mutations mimicking brainstem tectal gliomaM Rio, A S Lebre, P de Lonlay, et al.
Molecular Genetics and Metabolism|June 12, 2013
Renal transplantation in 4 patients with methylmalonic aciduria: a cell therapy for metabolic diseaseA Brassier, O Boyer, V Valayannopoulos, et al.
Journal of Medical Genetics|October 26, 2010
A common pattern of brain MRI imaging in mitochondrial diseases with complex I deficiencyA S Lebre, M Rio, L Faivre d'Arcier, et al.
Journal of Medical Genetics|May 7, 2013
Phenotype and genotype in 101 males with X-linked creatine transporter deficiencyJ M van de Kamp, O T Betsalel, S Mercimek-Mahmutoglu, et al.
Pageof 4