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M G Sweeney

Showing results (31-40 of 48) with videos related to

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Brain : a Journal of Neurology|August 1, 1992
Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutationA E Harding, M G Sweeney, D H Miller, et al.
Brain : a Journal of Neurology|April 29, 1998
The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlatesP Giunti, G Sabbadini, M G Sweeney, et al.
Biochimica Et Biophysica Acta|May 24, 1995
Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotypeJ A Morgan-Hughes, M G Sweeney, J M Cooper, et al.
Journal of the Neurological Sciences|January 1, 1992
Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathyS R Hammans, M G Sweeney, I J Holt, et al.
Brain : a Journal of Neurology|June 1, 1993
The mitochondrial DNA transfer RNA(Lys)A-->G(8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF). Relationship of clinical phenotype to proportion of mutant mitochondrial DNAS R Hammans, M G Sweeney, M Brockington, et al.
Neurology|January 2, 2008
What causes paramyotonia in the United Kingdom? Common and new SCN4A mutations revealedE Matthews, S V Tan, D Fialho, 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.
Neurology|January 2, 2009
Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysisE Matthews, R Labrum, M G Sweeney, 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.
Journal of Medical Genetics|December 7, 2007
Episodic ataxia and hemiplegia caused by the 8993T->C mitochondrial DNA mutationK Craig, H R Elliott, S M Keers, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Brain : a Journal of Neurology|August 1, 1992
Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutationA E Harding, M G Sweeney, D H Miller, et al.
Brain : a Journal of Neurology|April 29, 1998
The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlatesP Giunti, G Sabbadini, M G Sweeney, et al.
Biochimica Et Biophysica Acta|May 24, 1995
Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotypeJ A Morgan-Hughes, M G Sweeney, J M Cooper, et al.
Journal of the Neurological Sciences|January 1, 1992
Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathyS R Hammans, M G Sweeney, I J Holt, et al.
Brain : a Journal of Neurology|June 1, 1993
The mitochondrial DNA transfer RNA(Lys)A-->G(8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF). Relationship of clinical phenotype to proportion of mutant mitochondrial DNAS R Hammans, M G Sweeney, M Brockington, et al.
Neurology|January 2, 2008
What causes paramyotonia in the United Kingdom? Common and new SCN4A mutations revealedE Matthews, S V Tan, D Fialho, 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.
Neurology|January 2, 2009
Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysisE Matthews, R Labrum, M G Sweeney, 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.
Journal of Medical Genetics|December 7, 2007
Episodic ataxia and hemiplegia caused by the 8993T->C mitochondrial DNA mutationK Craig, H R Elliott, S M Keers, et al.
Pageof 5