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T Siddique

Showing results (31-40 of 69) with videos related to

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Journal of Neuropathology and Experimental Neurology|April 1, 1996
Intense superoxide dismutase-1 immunoreactivity in intracytoplasmic hyaline inclusions of familial amyotrophic lateral sclerosis with posterior column involvementN Shibata, A Hirano, M Kobayashi, et al.
The EMBO Journal|March 1, 1990
Alpha subunit variants of the human glycine receptor: primary structures, functional expression and chromosomal localization of the corresponding genesG Grenningloh, V Schmieden, P R Schofield, et al.
Clinical Genetics|June 1, 1989
Duchenne muscular dystrophy: detection of deletion carriers by spectrophotometric densitometryN G Laing, T Siddique, R Bartlett, et al.
Neurology|August 1, 1992
Intrafamilial heterogeneity in hereditary motor neuron diseaseJ S Appelbaum, R P Roos, E F Salazar-Grueso, et al.
Neurology|January 30, 2009
Age and founder effect of SOD1 A4V mutation causing ALSM Saeed, Y Yang, H-X Deng, et al.
Australian Paediatric Journal|January 1, 1988
Update on the molecular genetics of Duchenne muscular dystrophyT Siddique, R Bartlett, M Pericak-Vance, et al.
Journal of Neurophysiology|March 7, 2014
Effect of fluoxetine on disease progression in a mouse model of ALSJ E Koschnitzky, K A Quinlan, T J Lukas, et al.
Neurology|January 1, 1985
Autosomal dominant syndrome of lipid neuromyopathy with normal carnitine: successful treatment with long-chain fatty-acid-free dietV Askanas, W K Engel, H H Kwan, et al.
Human Molecular Genetics|August 1, 1994
Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneityA Hentati, M A Pericak-Vance, W Y Hung, et al.
American Journal of Medical Genetics|October 1, 1987
Chorea-acanthocytosis: a report of three new families and implications for genetic counsellingJ M Vance, M A Pericak-Vance, M H Bowman, et al.
Pageof 7

Showing results (31-40 of 69) with videos related to

Sort By:
Pageof 7
Journal of Neuropathology and Experimental Neurology|April 1, 1996
Intense superoxide dismutase-1 immunoreactivity in intracytoplasmic hyaline inclusions of familial amyotrophic lateral sclerosis with posterior column involvementN Shibata, A Hirano, M Kobayashi, et al.
The EMBO Journal|March 1, 1990
Alpha subunit variants of the human glycine receptor: primary structures, functional expression and chromosomal localization of the corresponding genesG Grenningloh, V Schmieden, P R Schofield, et al.
Clinical Genetics|June 1, 1989
Duchenne muscular dystrophy: detection of deletion carriers by spectrophotometric densitometryN G Laing, T Siddique, R Bartlett, et al.
Neurology|August 1, 1992
Intrafamilial heterogeneity in hereditary motor neuron diseaseJ S Appelbaum, R P Roos, E F Salazar-Grueso, et al.
Neurology|January 30, 2009
Age and founder effect of SOD1 A4V mutation causing ALSM Saeed, Y Yang, H-X Deng, et al.
Australian Paediatric Journal|January 1, 1988
Update on the molecular genetics of Duchenne muscular dystrophyT Siddique, R Bartlett, M Pericak-Vance, et al.
Journal of Neurophysiology|March 7, 2014
Effect of fluoxetine on disease progression in a mouse model of ALSJ E Koschnitzky, K A Quinlan, T J Lukas, et al.
Neurology|January 1, 1985
Autosomal dominant syndrome of lipid neuromyopathy with normal carnitine: successful treatment with long-chain fatty-acid-free dietV Askanas, W K Engel, H H Kwan, et al.
Human Molecular Genetics|August 1, 1994
Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneityA Hentati, M A Pericak-Vance, W Y Hung, et al.
American Journal of Medical Genetics|October 1, 1987
Chorea-acanthocytosis: a report of three new families and implications for genetic counsellingJ M Vance, M A Pericak-Vance, M H Bowman, et al.
Pageof 7