What's in a name? Amyotrophic lateral sclerosis, motor neuron disease, and allelic heterogeneity
- 1 June 1998
- journal article
- Published by Wiley in Annals of Neurology
- Vol. 43 (6) , 691-694
- https://doi.org/10.1002/ana.410430602
Abstract
No abstract availableThis publication has 41 references indexed in Scilit:
- Limited corticospinal tract involvement in amyotrophic lateral sclerosis subjects with the A4V mutation in the copper/zinc superoxide dismutase geneAnnals of Neurology, 1998
- A novel SOD1 mutation in an Austrian family with amyotrophic lateral sclerosisNeuromuscular Disorders, 1997
- Epidemiology of mutations in superoxide dismutase in amyotrophic lateal sclerosisAnnals of Neurology, 1997
- Sequence variants in human neurofilament proteins: Absence of linkage to familial amyotrophic lateral sclerosisAnnals of Neurology, 1996
- Difficulties in distinguishing sporadic from familial amyotrophic lateral sclerosisAnnals of Neurology, 1996
- Familial amyotrophic lateral sclerosis with a point mutation of SOD-1: intrafamilial heterogeneity of disease duration associated with neurofibrillary tangles.Journal of Neurology, Neurosurgery & Psychiatry, 1995
- Cu/Zn superoxide dismutase (SOD1) mutations and sporadic amyotrophic lateral sclerosisThe Lancet, 1993
- The central nervous system in motor neurone diseaseJournal of Neurology, Neurosurgery & Psychiatry, 1970
- AN INHERITED DISEASE SIMILAR TO AMYOTROPHIC LATERAL SCLEROSIS WITH A PATTERN OF POSTERIOR COLUMN INVOLVEMENT. AN INTERMEDIATE FORM?Brain, 1959