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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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F Pierelli

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Neurology|January 14, 2004

Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay typeG S Grieco, A Malandrini, G Comanducci, et al.

Neuroscience Letters|August 28, 2007

The wolframin His611Arg polymorphism influences medication overuse headacheC Di Lorenzo, G Sances, G Di Lorenzo, et al.

Neurology|March 29, 2001

Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish familyC Casali, V Bonifati, F M Santorelli, et al.

Neurology|April 26, 2006

Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic studyC Criscuolo, L Chessa, S Di Giandomenico, et al.

Pageof 12

Search research articles

Showing results (111-120 of 114) with videos related to

Sort By:

Pageof 12

You have reached the last page of results.This site can display upto 114 results.

Neurology|January 14, 2004

Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay typeG S Grieco, A Malandrini, G Comanducci, et al.

Neuroscience Letters|August 28, 2007

The wolframin His611Arg polymorphism influences medication overuse headacheC Di Lorenzo, G Sances, G Di Lorenzo, et al.

Neurology|March 29, 2001

Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish familyC Casali, V Bonifati, F M Santorelli, et al.

Neurology|April 26, 2006

Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic studyC Criscuolo, L Chessa, S Di Giandomenico, et al.

Pageof 12