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L Forsgren

Showing results (121-130 of 124) with videos related to

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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.
American Journal of Human Genetics|October 7, 2000
A major locus for myoclonus-dystonia maps to chromosome 7q in eight familiesC Klein, K Schilling, R J Saunders-Pullman, et al.
European Journal of Neurology|January 31, 2016
Management of dystonia in Europe: a survey of the European network for the study of the dystonia syndromesA Valadas, M-F Contarino, A Albanese, et al.
Annals of Neurology|March 15, 2000
Evaluation of the role of the D2 dopamine receptor in myoclonus dystoniaC Klein, N Gurvich, M Sena-Esteves, et al.
Pageof 13

Showing results (121-130 of 124) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 124 results.
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.
American Journal of Human Genetics|October 7, 2000
A major locus for myoclonus-dystonia maps to chromosome 7q in eight familiesC Klein, K Schilling, R J Saunders-Pullman, et al.
European Journal of Neurology|January 31, 2016
Management of dystonia in Europe: a survey of the European network for the study of the dystonia syndromesA Valadas, M-F Contarino, A Albanese, et al.
Annals of Neurology|March 15, 2000
Evaluation of the role of the D2 dopamine receptor in myoclonus dystoniaC Klein, N Gurvich, M Sena-Esteves, et al.
Pageof 13