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American Journal of Human Genetics
|
September 26, 2003
Slowed conduction and thin myelination of peripheral nerves associated with mutant rho Guanine-nucleotide exchange factor 10
Kristien Verhoeven, Peter De Jonghe, Tom Van de Putte, et al.
American Journal of Human Genetics
|
January 25, 2003
Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy
Kristien Verhoeven, Peter De Jonghe, Katrien Coen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 7, 2007
Astrocytes regulate GluR2 expression in motor neurons and their vulnerability to excitotoxicity
Philip Van Damme, Elke Bogaert, Maarten Dewil, et al.
Nature Genetics
|
February 26, 2005
Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease
Stephan Züchner, Maher Noureddine, Marina Kennerson, et al.
Molecular and Cellular Neurosciences
|
September 6, 2005
Synaptopodin and 4 novel genes identified in primary sensory neurons
Nathalie Verpoorten, Kristien Verhoeven, Stefan Weckx, et al.
Brain : a Journal of Neurology
|
June 9, 2009
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy
Kristl G Claeys, Stephan Züchner, Marina Kennerson, et al.
Annals of Neurology
|
January 27, 2006
Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2
Stephan Züchner, Peter De Jonghe, Albena Jordanova, et al.
Brain : a Journal of Neurology
|
May 23, 2006
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2
Kristien Verhoeven, Kristl G Claeys, Stephan Züchner, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 18) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 18 results.
American Journal of Human Genetics
|
September 26, 2003
Slowed conduction and thin myelination of peripheral nerves associated with mutant rho Guanine-nucleotide exchange factor 10
Kristien Verhoeven, Peter De Jonghe, Tom Van de Putte, et al.
American Journal of Human Genetics
|
January 25, 2003
Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy
Kristien Verhoeven, Peter De Jonghe, Katrien Coen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 7, 2007
Astrocytes regulate GluR2 expression in motor neurons and their vulnerability to excitotoxicity
Philip Van Damme, Elke Bogaert, Maarten Dewil, et al.
Nature Genetics
|
February 26, 2005
Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease
Stephan Züchner, Maher Noureddine, Marina Kennerson, et al.
Molecular and Cellular Neurosciences
|
September 6, 2005
Synaptopodin and 4 novel genes identified in primary sensory neurons
Nathalie Verpoorten, Kristien Verhoeven, Stefan Weckx, et al.
Brain : a Journal of Neurology
|
June 9, 2009
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy
Kristl G Claeys, Stephan Züchner, Marina Kennerson, et al.
Annals of Neurology
|
January 27, 2006
Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2
Stephan Züchner, Peter De Jonghe, Albena Jordanova, et al.
Brain : a Journal of Neurology
|
May 23, 2006
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2
Kristien Verhoeven, Kristl G Claeys, Stephan Züchner, et al.
Page
of 2