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K M Flanigan

Showing results (1-10 of 22) with videos related to

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Journal of Clinical Neuromuscular Disease|December 17, 2008
Genetic testing in the neuromuscular clinicK M Flanigan
Neurology|December 1, 1993
Association of the 11778 mitochondrial DNA mutation and demyelinating diseaseK M Flanigan, D R Johns
Neurologic Clinics|July 17, 1998
Age-related biology and diseases of muscle and nerveK M Flanigan, G Lauria, J W Griffin, et al.
Neuropathology and Applied Neurobiology|January 17, 2012
Quantification of dystrophin immunofluorescence in dystrophinopathy muscle specimensL E Taylor, Y J Kaminoh, C K Rodesch, et al.
Neurology|July 29, 2011
Neurology Academic Advisory Committee: a strategy for faculty retention and advancementT Schenkenberg, N L Foster, M B Bromberg, et al.
Neuromuscular Disorders : NMD|August 30, 2001
Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophyK M Flanigan, C M Coffeen, L Sexton, et al.
Neurology|October 16, 1999
Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24N M Plaster, E Uyama, M Uchino, et al.
Annals of Neurology|August 12, 2000
Sequence specificity of aminoglycoside-induced stop condon readthrough: potential implications for treatment of Duchenne muscular dystrophyM T Howard, B H Shirts, L M Petros, et al.
AJNR. American Journal of Neuroradiology|February 12, 1998
AIDS-related MR hyperintensity of the basal gangliaC C Meltzer, S W Wells, M W Becher, et al.
Neuromuscular Disorders : NMD|March 6, 2007
Paraneoplastic myopathy: response to intravenous immunoglobulinJ B Sampson, S M Smith, A G Smith, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Journal of Clinical Neuromuscular Disease|December 17, 2008
Genetic testing in the neuromuscular clinicK M Flanigan
Neurology|December 1, 1993
Association of the 11778 mitochondrial DNA mutation and demyelinating diseaseK M Flanigan, D R Johns
Neurologic Clinics|July 17, 1998
Age-related biology and diseases of muscle and nerveK M Flanigan, G Lauria, J W Griffin, et al.
Neuropathology and Applied Neurobiology|January 17, 2012
Quantification of dystrophin immunofluorescence in dystrophinopathy muscle specimensL E Taylor, Y J Kaminoh, C K Rodesch, et al.
Neurology|July 29, 2011
Neurology Academic Advisory Committee: a strategy for faculty retention and advancementT Schenkenberg, N L Foster, M B Bromberg, et al.
Neuromuscular Disorders : NMD|August 30, 2001
Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophyK M Flanigan, C M Coffeen, L Sexton, et al.
Neurology|October 16, 1999
Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24N M Plaster, E Uyama, M Uchino, et al.
Annals of Neurology|August 12, 2000
Sequence specificity of aminoglycoside-induced stop condon readthrough: potential implications for treatment of Duchenne muscular dystrophyM T Howard, B H Shirts, L M Petros, et al.
AJNR. American Journal of Neuroradiology|February 12, 1998
AIDS-related MR hyperintensity of the basal gangliaC C Meltzer, S W Wells, M W Becher, et al.
Neuromuscular Disorders : NMD|March 6, 2007
Paraneoplastic myopathy: response to intravenous immunoglobulinJ B Sampson, S M Smith, A G Smith, et al.
Pageof 3