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Shirley Rainier

Showing results (1-10 of 9) with videos related to

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Archives of Neurology|September 15, 2005
Cerebrotendinous xanthomatosis: possible higher prevalence than previously recognizedMatthew T Lorincz, Shirley Rainier, Donald Thomas, et al.
Plos One|December 17, 2015
Delayed Induction of Human NTE (PNPLA6) Rescues Neurodegeneration and Mobility Defects of Drosophila swiss cheese (sws) MutantsAlyson Sujkowski, Shirley Rainier, John K Fink, et al.
Journal of Neurogenetics|December 17, 2008
Normal dopaminergic nigrostriatal innervation in SPG3A hereditary spastic paraplegiaRoger L Albin, Robert A Koeppe, Shirley Rainier, et al.
Archives of Neurology|March 15, 2006
De novo occurrence of novel SPG3A/atlastin mutation presenting as cerebral palsyShirley Rainier, Carron Sher, Orit Reish, et al.
American Journal of Human Genetics|September 26, 2003
NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6)Shirley Rainier, Jing-Hua Chai, Debra Tokarz, et al.
Muscle & Nerve|December 21, 2010
Motor neuron disease due to neuropathy target esterase gene mutation: clinical features of the index familiesShirley Rainier, James W Albers, Peter J Dyck, et al.
Archives of Neurology|April 13, 2005
Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindredsDong-Hui Chen, Mark Matsushita, Shirley Rainier, et al.
Archives of Neurology|July 21, 2004
Myofibrillogenesis regulator 1 gene mutations cause paroxysmal dystonic choreoathetosisShirley Rainier, Donald Thomas, Debra Tokarz, et al.
American Journal of Human Genetics|March 4, 2008
Neuropathy target esterase gene mutations cause motor neuron diseaseShirley Rainier, Melanie Bui, Erin Mark, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Archives of Neurology|September 15, 2005
Cerebrotendinous xanthomatosis: possible higher prevalence than previously recognizedMatthew T Lorincz, Shirley Rainier, Donald Thomas, et al.
Plos One|December 17, 2015
Delayed Induction of Human NTE (PNPLA6) Rescues Neurodegeneration and Mobility Defects of Drosophila swiss cheese (sws) MutantsAlyson Sujkowski, Shirley Rainier, John K Fink, et al.
Journal of Neurogenetics|December 17, 2008
Normal dopaminergic nigrostriatal innervation in SPG3A hereditary spastic paraplegiaRoger L Albin, Robert A Koeppe, Shirley Rainier, et al.
Archives of Neurology|March 15, 2006
De novo occurrence of novel SPG3A/atlastin mutation presenting as cerebral palsyShirley Rainier, Carron Sher, Orit Reish, et al.
American Journal of Human Genetics|September 26, 2003
NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6)Shirley Rainier, Jing-Hua Chai, Debra Tokarz, et al.
Muscle & Nerve|December 21, 2010
Motor neuron disease due to neuropathy target esterase gene mutation: clinical features of the index familiesShirley Rainier, James W Albers, Peter J Dyck, et al.
Archives of Neurology|April 13, 2005
Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindredsDong-Hui Chen, Mark Matsushita, Shirley Rainier, et al.
Archives of Neurology|July 21, 2004
Myofibrillogenesis regulator 1 gene mutations cause paroxysmal dystonic choreoathetosisShirley Rainier, Donald Thomas, Debra Tokarz, et al.
American Journal of Human Genetics|March 4, 2008
Neuropathy target esterase gene mutations cause motor neuron diseaseShirley Rainier, Melanie Bui, Erin Mark, et al.
Pageof 1