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

C Guiraud-Chaumeil

Showing results (1-10 of 12) with videos related to

Pageof 2
Sort By:
Revue Neurologique|April 25, 2001
[Hemicontracture and facial myokimia as the first manifestation of multiple sclerosis]A Dupeyron, F Chaury, C Guiraud-Chaumeil, et al.
Presse Medicale (Paris, France : 1983)|April 21, 1999
[Spinocerebellar ataxia and polyneuropathy secondary to vitamin E deficiency]C Guiraud-Chaumeil, F Battaglia, C Tranchant, et al.
Journal of Neurology|January 11, 2001
Is clonidine growth hormone stimulation a good test to differentiate multiple system atrophy from idiopathic Parkinson's disease?C Tranchant, C Guiraud-Chaumeil, A Echaniz-Laguna, et al.
Human Mutation|February 5, 1998
Confirmation of prenatal diagnosis results of X-linked recessive myotubular myopathy by mutational screening, and description of three new mutations in the MTM1 geneS M Tanner, J Laporte, C Guiraud-Chaumeil, et al.
Revue Neurologique|December 19, 2000
[Myotubular myopathy]C Guiraud-Chaumeil, J Laporte, J L Mandel, et al.
Neurology|April 24, 1999
Basis of phenotypic variability in sporadic Creutzfeldt-Jakob diseaseC Tranchant, L Geranton, C Guiraud-Chaumeil, et al.
Journal of Medical Genetics|April 16, 1998
Extensive germinal mosaicism in a family with X linked myotubular myopathy simulates genetic heterogeneityM C Vincent, C Guiraud-Chaumeil, J Laporte, et al.
American Journal of Human Genetics|June 1, 1997
A mutation in the MTM1 gene invalidates a previous suggestion of nonallelic heterogeneity in X-linked myotubular myopathyC Guiraud-Chaumeil, M C Vincent, J Laporte, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Homozygosity mapping of spinocerebellar ataxia with cerebellar atrophy and peripheral neuropathy to 9q33-34, and with hearing impairment and optic atrophy to 6p21-23P Bomont, M Watanabe, R Gershoni-Barush, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|February 27, 1999
[Spinal cord MRI in multiple sclerosis: comparison of turbo-spin echo sequences and turbo-MRI]C Neugroschl, S von Sohsten, A Doll, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Revue Neurologique|April 25, 2001
[Hemicontracture and facial myokimia as the first manifestation of multiple sclerosis]A Dupeyron, F Chaury, C Guiraud-Chaumeil, et al.
Presse Medicale (Paris, France : 1983)|April 21, 1999
[Spinocerebellar ataxia and polyneuropathy secondary to vitamin E deficiency]C Guiraud-Chaumeil, F Battaglia, C Tranchant, et al.
Journal of Neurology|January 11, 2001
Is clonidine growth hormone stimulation a good test to differentiate multiple system atrophy from idiopathic Parkinson's disease?C Tranchant, C Guiraud-Chaumeil, A Echaniz-Laguna, et al.
Human Mutation|February 5, 1998
Confirmation of prenatal diagnosis results of X-linked recessive myotubular myopathy by mutational screening, and description of three new mutations in the MTM1 geneS M Tanner, J Laporte, C Guiraud-Chaumeil, et al.
Revue Neurologique|December 19, 2000
[Myotubular myopathy]C Guiraud-Chaumeil, J Laporte, J L Mandel, et al.
Neurology|April 24, 1999
Basis of phenotypic variability in sporadic Creutzfeldt-Jakob diseaseC Tranchant, L Geranton, C Guiraud-Chaumeil, et al.
Journal of Medical Genetics|April 16, 1998
Extensive germinal mosaicism in a family with X linked myotubular myopathy simulates genetic heterogeneityM C Vincent, C Guiraud-Chaumeil, J Laporte, et al.
American Journal of Human Genetics|June 1, 1997
A mutation in the MTM1 gene invalidates a previous suggestion of nonallelic heterogeneity in X-linked myotubular myopathyC Guiraud-Chaumeil, M C Vincent, J Laporte, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Homozygosity mapping of spinocerebellar ataxia with cerebellar atrophy and peripheral neuropathy to 9q33-34, and with hearing impairment and optic atrophy to 6p21-23P Bomont, M Watanabe, R Gershoni-Barush, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|February 27, 1999
[Spinal cord MRI in multiple sclerosis: comparison of turbo-spin echo sequences and turbo-MRI]C Neugroschl, S von Sohsten, A Doll, et al.
Pageof 2