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P M Andersen

Showing results (51-60 of 61) with videos related to

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Brain : a Journal of Neurology|August 1, 1996
Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patientsP M Andersen, L Forsgren, M Binzer, et al.
Neurology|June 30, 2006
ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)N Parkinson, P G Ince, M O Smith, et al.
Neurology|August 13, 2008
Association of paraoxonase gene cluster polymorphisms with ALS in France, Quebec, and SwedenP N Valdmanis, E Kabashi, A Dyck, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 26, 2011
Differential corticospinal tract degeneration in homozygous 'D90A' SOD-1 ALS and sporadic ALSC R V Blain, S Brunton, V C Williams, et al.
Neurology|January 20, 2006
A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementiaM Morita, A Al-Chalabi, P M Andersen, et al.
Neurology|November 18, 2005
Rapid disease progression correlates with instability of mutant SOD1 in familial ALST Sato, T Nakanishi, Y Yamamoto, et al.
European Journal of Human Genetics : EJHG|July 4, 2001
Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the worldA Lund, B Udd, V Juvonen, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|March 21, 2007
Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypesJ C Schymick, Y Yang, P M Andersen, et al.
Neurology|March 27, 2009
A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALSA-M Wills, S Cronin, A Slowik, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Brain : a Journal of Neurology|August 1, 1996
Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patientsP M Andersen, L Forsgren, M Binzer, et al.
Neurology|June 30, 2006
ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)N Parkinson, P G Ince, M O Smith, et al.
Neurology|August 13, 2008
Association of paraoxonase gene cluster polymorphisms with ALS in France, Quebec, and SwedenP N Valdmanis, E Kabashi, A Dyck, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 26, 2011
Differential corticospinal tract degeneration in homozygous 'D90A' SOD-1 ALS and sporadic ALSC R V Blain, S Brunton, V C Williams, et al.
Neurology|January 20, 2006
A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementiaM Morita, A Al-Chalabi, P M Andersen, et al.
Neurology|November 18, 2005
Rapid disease progression correlates with instability of mutant SOD1 in familial ALST Sato, T Nakanishi, Y Yamamoto, et al.
European Journal of Human Genetics : EJHG|July 4, 2001
Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the worldA Lund, B Udd, V Juvonen, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|March 21, 2007
Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypesJ C Schymick, Y Yang, P M Andersen, et al.
Neurology|March 27, 2009
A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALSA-M Wills, S Cronin, A Slowik, et al.
Pageof 7