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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 gene
S 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 disease
C 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 heterogeneity
M 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 myopathy
C 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 6p21-23
P 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.
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Search research articles
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Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 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 gene
S 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 disease
C 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 heterogeneity
M 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 myopathy
C 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 6p21-23
P 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.
Page
of 2