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G Sweeney

Showing results (161-170 of 220) with videos related to

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Forensic Science International|May 12, 2001
A survey of extraction techniques for drugs of abuse in urineJ F Wilson, B L Smith, P A Toseland, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 29, 2013
The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis and managementVictoria Nesbitt, Robert D S Pitceathly, Doug M Turnbull, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 3, 2011
An intragenic duplication in guanosine triphosphate cyclohydrolase-1 gene in a dopa-responsive dystonia familyHelen Ling, James M Polke, Mary G Sweeney, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 9, 2008
Huntington's disease phenocopies are clinically and genetically heterogeneousEdward J Wild, Ese E Mudanohwo, Mary G Sweeney, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2004
Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern IndiaK K Sinha, P F Worth, D K Jha, et al.
Plos Genetics|August 13, 2013
The role of interruptions in polyQ in the pathology of SCA1Rajesh P Menon, Suran Nethisinghe, Serena Faggiano, et al.
Neurology|January 2, 2009
Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysisE Matthews, R Labrum, M G Sweeney, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2010
An ITPR1 gene deletion causes spinocerebellar ataxia 15/16: a genetic, clinical and radiological descriptionMarianne J U Novak, Mary G Sweeney, Abi Li, et al.
Brain : a Journal of Neurology|March 1, 1997
The phenotypic manifestations of chromosome 17p11.2 duplicationP K Thomas, W Marques, M B Davis, et al.
JAMA|September 9, 1988
Fatal food-induced anaphylaxisJ W Yunginger, K G Sweeney, W Q Sturner, et al.
Pageof 22

Showing results (161-170 of 220) with videos related to

Sort By:
Pageof 22
Forensic Science International|May 12, 2001
A survey of extraction techniques for drugs of abuse in urineJ F Wilson, B L Smith, P A Toseland, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 29, 2013
The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis and managementVictoria Nesbitt, Robert D S Pitceathly, Doug M Turnbull, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 3, 2011
An intragenic duplication in guanosine triphosphate cyclohydrolase-1 gene in a dopa-responsive dystonia familyHelen Ling, James M Polke, Mary G Sweeney, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 9, 2008
Huntington's disease phenocopies are clinically and genetically heterogeneousEdward J Wild, Ese E Mudanohwo, Mary G Sweeney, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2004
Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern IndiaK K Sinha, P F Worth, D K Jha, et al.
Plos Genetics|August 13, 2013
The role of interruptions in polyQ in the pathology of SCA1Rajesh P Menon, Suran Nethisinghe, Serena Faggiano, et al.
Neurology|January 2, 2009
Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysisE Matthews, R Labrum, M G Sweeney, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2010
An ITPR1 gene deletion causes spinocerebellar ataxia 15/16: a genetic, clinical and radiological descriptionMarianne J U Novak, Mary G Sweeney, Abi Li, et al.
Brain : a Journal of Neurology|March 1, 1997
The phenotypic manifestations of chromosome 17p11.2 duplicationP K Thomas, W Marques, M B Davis, et al.
JAMA|September 9, 1988
Fatal food-induced anaphylaxisJ W Yunginger, K G Sweeney, W Q Sturner, et al.
Pageof 22