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Kristien Verhoeven

Showing results (11-20 of 18) with videos related to

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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 10Kristien 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 neuropathyKristien 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 excitotoxicityPhilip 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 diseaseStephan Züchner, Maher Noureddine, Marina Kennerson, et al.
Molecular and Cellular Neurosciences|September 6, 2005
Synaptopodin and 4 novel genes identified in primary sensory neuronsNathalie 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 neuropathyKristl 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 2Stephan 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 2Kristien Verhoeven, Kristl G Claeys, Stephan Züchner, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 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 10Kristien 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 neuropathyKristien 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 excitotoxicityPhilip 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 diseaseStephan Züchner, Maher Noureddine, Marina Kennerson, et al.
Molecular and Cellular Neurosciences|September 6, 2005
Synaptopodin and 4 novel genes identified in primary sensory neuronsNathalie 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 neuropathyKristl 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 2Stephan 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 2Kristien Verhoeven, Kristl G Claeys, Stephan Züchner, et al.
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