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J M Burgunder

Showing results (81-90 of 100) with videos related to

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Epilepsy Research|July 13, 2004
Metabotropic glutamate receptor 2/3 in the hippocampus of patients with mesial temporal lobe epilepsy, and of rats and mice after pilocarpine-induced status epilepticusF R Tang, S C Chia, P M Chen, et al.
European Journal of Neurology|May 1, 2013
EFNS review on the role of muscle biopsy in the investigation of myalgiaT Kyriakides, C Angelini, J Schaefer, et al.
European Journal of Neurology|September 13, 2017
Characterization of social cognition impairment in multiple sclerosisM Neuhaus, S Bagutti, Ö Yaldizli, et al.
Journal of Neurology|February 13, 2007
Mitochondrial neurogastrointestinal encephalomyopathy in three siblings: clinical, genetic and neuroradiological featuresW M M Schüpbach, K Madhavi Vadday, A Schaller, et al.
Parkinsonism & Related Disorders|April 3, 2019
Stimulation of the globus pallidus internus in the treatment of Parkinson's disease: Long-term results of a monocentric cohortM L Lachenmayer, C Bettschen, C Bernasconi, et al.
Neuromuscular Disorders : NMD|January 5, 2000
A diagnostic fluorescent marker kit for six limb girdle muscular dystrophiesI Richard, N Bourg, S Marchand, et al.
European Journal of Neurology|January 19, 2008
LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland ChinaX-K An, R Peng, T Li, et al.
Neuroscience Letters|July 22, 2008
Lack of evidence for association of a UCH-L1 S18Y polymorphism with Parkinson's disease in a Han-Chinese populationZ-J Zhang, J-M Burgunder, X-K An, et al.
Brain : a Journal of Neurology|October 1, 1996
Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2A Dürr, C S Davoine, C Paternotte, et al.
Nature Genetics|December 28, 1999
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegiaJ Hazan, N Fonknechten, D Mavel, et al.
Pageof 10

Showing results (81-90 of 100) with videos related to

Sort By:
Pageof 10
Epilepsy Research|July 13, 2004
Metabotropic glutamate receptor 2/3 in the hippocampus of patients with mesial temporal lobe epilepsy, and of rats and mice after pilocarpine-induced status epilepticusF R Tang, S C Chia, P M Chen, et al.
European Journal of Neurology|May 1, 2013
EFNS review on the role of muscle biopsy in the investigation of myalgiaT Kyriakides, C Angelini, J Schaefer, et al.
European Journal of Neurology|September 13, 2017
Characterization of social cognition impairment in multiple sclerosisM Neuhaus, S Bagutti, Ö Yaldizli, et al.
Journal of Neurology|February 13, 2007
Mitochondrial neurogastrointestinal encephalomyopathy in three siblings: clinical, genetic and neuroradiological featuresW M M Schüpbach, K Madhavi Vadday, A Schaller, et al.
Parkinsonism & Related Disorders|April 3, 2019
Stimulation of the globus pallidus internus in the treatment of Parkinson's disease: Long-term results of a monocentric cohortM L Lachenmayer, C Bettschen, C Bernasconi, et al.
Neuromuscular Disorders : NMD|January 5, 2000
A diagnostic fluorescent marker kit for six limb girdle muscular dystrophiesI Richard, N Bourg, S Marchand, et al.
European Journal of Neurology|January 19, 2008
LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland ChinaX-K An, R Peng, T Li, et al.
Neuroscience Letters|July 22, 2008
Lack of evidence for association of a UCH-L1 S18Y polymorphism with Parkinson's disease in a Han-Chinese populationZ-J Zhang, J-M Burgunder, X-K An, et al.
Brain : a Journal of Neurology|October 1, 1996
Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2A Dürr, C S Davoine, C Paternotte, et al.
Nature Genetics|December 28, 1999
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegiaJ Hazan, N Fonknechten, D Mavel, et al.
Pageof 10