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P M Andersen

Showing results (41-50 of 61) with videos related to

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European Journal of Neurology|December 6, 2005
EFNS task force on management of amyotrophic lateral sclerosis: guidelines for diagnosing and clinical care of patients and relativesP M Andersen, G D Borasio, R Dengler, et al.
Brain : a Journal of Neurology|November 20, 1997
Phenotypic heterogeneity in motor neuron disease patients with CuZn-superoxide dismutase mutations in ScandinaviaP M Andersen, P Nilsson, M L Keränen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 25, 2011
ALS patients with SOD1 mutations in Switzerland show very diverse phenotypes and extremely long survivalM Weber, C Neuwirth, J Thierbach, et al.
Human Molecular Genetics|February 5, 1999
Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosisA Al-Chalabi, P M Andersen, P Nilsson, et al.
European Journal of Neurology|December 11, 2012
Truncating mutations in FUS/TLS give rise to a more aggressive ALS-phenotype than missense mutations: a clinico-genetic study in GermanyS Waibel, M Neumann, A Rosenbohm, et al.
Nature Genetics|May 1, 1995
Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutaseP M Andersen, P Nilsson, V Ala-Hurula, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2005
Abnormal cortical excitability in sporadic but not homozygous D90A SOD1 ALSM R Turner, A D Osei-Lah, A Hammers, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Founder effect in spinal and bulbar muscular atrophy (SBMA) in ScandinaviaA Lund, B Udd, V Juvonen, et al.
Neurology|December 30, 2004
No association of the SOD1 locus and disease susceptibility or phenotype in sporadic ALSW J Broom, M J Parton, C A Vance, et al.
Neuroscience Letters|December 7, 2007
SOD1A4V-mediated ALS: absence of a closely linked modifier gene and origination in AsiaW J Broom, D V Johnson, K E Auwarter, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
European Journal of Neurology|December 6, 2005
EFNS task force on management of amyotrophic lateral sclerosis: guidelines for diagnosing and clinical care of patients and relativesP M Andersen, G D Borasio, R Dengler, et al.
Brain : a Journal of Neurology|November 20, 1997
Phenotypic heterogeneity in motor neuron disease patients with CuZn-superoxide dismutase mutations in ScandinaviaP M Andersen, P Nilsson, M L Keränen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 25, 2011
ALS patients with SOD1 mutations in Switzerland show very diverse phenotypes and extremely long survivalM Weber, C Neuwirth, J Thierbach, et al.
Human Molecular Genetics|February 5, 1999
Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosisA Al-Chalabi, P M Andersen, P Nilsson, et al.
European Journal of Neurology|December 11, 2012
Truncating mutations in FUS/TLS give rise to a more aggressive ALS-phenotype than missense mutations: a clinico-genetic study in GermanyS Waibel, M Neumann, A Rosenbohm, et al.
Nature Genetics|May 1, 1995
Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutaseP M Andersen, P Nilsson, V Ala-Hurula, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2005
Abnormal cortical excitability in sporadic but not homozygous D90A SOD1 ALSM R Turner, A D Osei-Lah, A Hammers, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Founder effect in spinal and bulbar muscular atrophy (SBMA) in ScandinaviaA Lund, B Udd, V Juvonen, et al.
Neurology|December 30, 2004
No association of the SOD1 locus and disease susceptibility or phenotype in sporadic ALSW J Broom, M J Parton, C A Vance, et al.
Neuroscience Letters|December 7, 2007
SOD1A4V-mediated ALS: absence of a closely linked modifier gene and origination in AsiaW J Broom, D V Johnson, K E Auwarter, et al.
Pageof 7