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T Siddique

Showing results (61-70 of 69) with videos related to

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Neurology|June 1, 1996
Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working groupJ K Fink, T Heiman-Patterson, T Bird, et al.
Neurogenetics|March 29, 2000
Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosisT Siddique, M A Pericak-Vance, J Caliendo, et al.
Nature Genetics|October 5, 2001
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosisY Yang, A Hentati, H X Deng, et al.
Human Molecular Genetics|November 18, 1998
Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factorA Al-Chalabi, P M Andersen, B Chioza, et al.
Neurology|November 23, 2000
Novel mutations in spastin gene and absence of correlation with age at onset of symptomsA Hentati, H X Deng, H Zhai, et al.
JAMA|October 4, 2000
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22B A Hosler, T Siddique, P C Sapp, et al.
Neurology|August 3, 1999
Neurodegenerative diseases of Guam: analysis of TAUJ Pérez-Tur, L Buée, H R Morris, et al.
Journal of Medical Genetics|April 17, 2008
Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the -2578AA genotypeD Lambrechts, K Poesen, R Fernández-Santiago, et al.
Science (New York, N.Y.)|March 3, 2009
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosisT J Kwiatkowski, D A Bosco, A L Leclerc, et al.
Pageof 7

Showing results (61-70 of 69) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 69 results.
Neurology|June 1, 1996
Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working groupJ K Fink, T Heiman-Patterson, T Bird, et al.
Neurogenetics|March 29, 2000
Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosisT Siddique, M A Pericak-Vance, J Caliendo, et al.
Nature Genetics|October 5, 2001
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosisY Yang, A Hentati, H X Deng, et al.
Human Molecular Genetics|November 18, 1998
Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factorA Al-Chalabi, P M Andersen, B Chioza, et al.
Neurology|November 23, 2000
Novel mutations in spastin gene and absence of correlation with age at onset of symptomsA Hentati, H X Deng, H Zhai, et al.
JAMA|October 4, 2000
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22B A Hosler, T Siddique, P C Sapp, et al.
Neurology|August 3, 1999
Neurodegenerative diseases of Guam: analysis of TAUJ Pérez-Tur, L Buée, H R Morris, et al.
Journal of Medical Genetics|April 17, 2008
Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the -2578AA genotypeD Lambrechts, K Poesen, R Fernández-Santiago, et al.
Science (New York, N.Y.)|March 3, 2009
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosisT J Kwiatkowski, D A Bosco, A L Leclerc, et al.
Pageof 7