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

R Amouri

Showing results (1-10 of 23) with videos related to

Pageof 3
Sort By:
Neuromuscular Disorders : NMD|April 18, 2006
Genetic heterogeneity within a consanguineous family involving the LGMD 2D and the LGMD 2C genesK Fendri, M Kefi, F Hentati, et al.
Journal of Inherited Metabolic Disease|September 10, 2008
L-2-hydroxyglutaric aciduria: clinical and molecular study in three Tunisian families. Identification of a new mutation and inter-familial phenotype variabilityA Larnaout, R Amouri, M Kefi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Distinct phenotypes within autosomal recessive ataxias not linked to already known lociY Bouhlal, G El-Euch-Fayeche, R Amouri, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|May 7, 2002
Association of a gliotoxic activity with active multiple sclerosis in US patientsR Pierig, J Belliveau, R Amouri, et al.
Neuropediatrics|August 2, 2008
Variable cardiac involvement in Tunisian siblings harboring FKRP gene mutationsM Kefi, R Amouri, S Chabrak, et al.
Neuroscience Letters|May 24, 1996
Mouse G2-GPI AChE is processed as a membrane-bound ectoenzyme in transfected mouse sarcoma cells but is not a homophilic adhesion moleculeM Guenneugues, M Verdière-Sahuqué, R Amouri, et al.
Neuromuscular Disorders : NMD|April 19, 2005
Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathyR Amouri, A Driss, K Murayama, et al.
Journal of Inherited Metabolic Disease|October 6, 2007
Osteoma of the calvaria in L-2-hydroxyglutaric aciduriaA Larnaout, R Amouri, S Neji, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3C Barhoumi, R Amouri, C Ben Hamida, et al.
Neuromuscular Disorders : NMD|December 18, 2003
Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutationM Kefi, R Amouri, A Driss, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Neuromuscular Disorders : NMD|April 18, 2006
Genetic heterogeneity within a consanguineous family involving the LGMD 2D and the LGMD 2C genesK Fendri, M Kefi, F Hentati, et al.
Journal of Inherited Metabolic Disease|September 10, 2008
L-2-hydroxyglutaric aciduria: clinical and molecular study in three Tunisian families. Identification of a new mutation and inter-familial phenotype variabilityA Larnaout, R Amouri, M Kefi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Distinct phenotypes within autosomal recessive ataxias not linked to already known lociY Bouhlal, G El-Euch-Fayeche, R Amouri, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|May 7, 2002
Association of a gliotoxic activity with active multiple sclerosis in US patientsR Pierig, J Belliveau, R Amouri, et al.
Neuropediatrics|August 2, 2008
Variable cardiac involvement in Tunisian siblings harboring FKRP gene mutationsM Kefi, R Amouri, S Chabrak, et al.
Neuroscience Letters|May 24, 1996
Mouse G2-GPI AChE is processed as a membrane-bound ectoenzyme in transfected mouse sarcoma cells but is not a homophilic adhesion moleculeM Guenneugues, M Verdière-Sahuqué, R Amouri, et al.
Neuromuscular Disorders : NMD|April 19, 2005
Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathyR Amouri, A Driss, K Murayama, et al.
Journal of Inherited Metabolic Disease|October 6, 2007
Osteoma of the calvaria in L-2-hydroxyglutaric aciduriaA Larnaout, R Amouri, S Neji, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3C Barhoumi, R Amouri, C Ben Hamida, et al.
Neuromuscular Disorders : NMD|December 18, 2003
Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutationM Kefi, R Amouri, A Driss, et al.
Pageof 3