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European Radiology
|
April 4, 2007
Diffusion-weighted imaging in normal fetal brain maturation
J F Schneider, S Confort-Gouny, Y Le Fur, et al.
Neurosurgery
|
February 1, 1997
The in vivo metabolic pattern of low-grade brain gliomas: a positron emission tomographic study using 18F-fluorodeoxyglucose and 11C-L-methylmethionine
J M Derlon, M C Petit-Taboué, F Chapon, et al.
Human Mutation
|
January 1, 1995
Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B
P Latour, F Blanquet, E Nelis, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1994
Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations
E Plassart, J Reboul, C S Rime, et al.
European Journal of Neurology
|
November 29, 2013
Intrafamilial heterogeneous clinical presentation of the mitochondrial 3243 MELAS mutation; molecular investigations among four generations
F Degoul, M Diry, F Viader, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1996
Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1A
F Chapon, P Diraison, B Lechevalier, et al.
Mutagenesis
|
August 18, 2005
Screening of TP53 mutations by DHPLC and sequencing in brain tumours from patients with an occupational exposure to pesticides or organic solvents
V Loyant, A Jaffré, J Breton, et al.
AJNR. American Journal of Neuroradiology
|
July 16, 2011
Is brain maturation comparable in fetuses and premature neonates at term equivalent age?
A Viola, S Confort-Gouny, J F Schneider, et al.
Biochemical and Biophysical Research Communications
|
September 1, 2007
A novel mutation 3090 G>A of the mitochondrial 16S ribosomal RNA associated with myopathy
L Coulbault, B Deslandes, D Herlicoviez, et al.
American Journal of Physiology. Cell Physiology
|
July 3, 2009
Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubes
S Sacconi, D Simkin, N Arrighi, et al.
Page
of 11
Search research articles
Search
Showing results (71-80 of 104) with videos related to
Sort By:
Page
of 11
European Radiology
|
April 4, 2007
Diffusion-weighted imaging in normal fetal brain maturation
J F Schneider, S Confort-Gouny, Y Le Fur, et al.
Neurosurgery
|
February 1, 1997
The in vivo metabolic pattern of low-grade brain gliomas: a positron emission tomographic study using 18F-fluorodeoxyglucose and 11C-L-methylmethionine
J M Derlon, M C Petit-Taboué, F Chapon, et al.
Human Mutation
|
January 1, 1995
Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B
P Latour, F Blanquet, E Nelis, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1994
Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations
E Plassart, J Reboul, C S Rime, et al.
European Journal of Neurology
|
November 29, 2013
Intrafamilial heterogeneous clinical presentation of the mitochondrial 3243 MELAS mutation; molecular investigations among four generations
F Degoul, M Diry, F Viader, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1996
Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1A
F Chapon, P Diraison, B Lechevalier, et al.
Mutagenesis
|
August 18, 2005
Screening of TP53 mutations by DHPLC and sequencing in brain tumours from patients with an occupational exposure to pesticides or organic solvents
V Loyant, A Jaffré, J Breton, et al.
AJNR. American Journal of Neuroradiology
|
July 16, 2011
Is brain maturation comparable in fetuses and premature neonates at term equivalent age?
A Viola, S Confort-Gouny, J F Schneider, et al.
Biochemical and Biophysical Research Communications
|
September 1, 2007
A novel mutation 3090 G>A of the mitochondrial 16S ribosomal RNA associated with myopathy
L Coulbault, B Deslandes, D Herlicoviez, et al.
American Journal of Physiology. Cell Physiology
|
July 3, 2009
Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubes
S Sacconi, D Simkin, N Arrighi, et al.
Page
of 11