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Annals of Neurology|June 1, 1996
Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patientsF M Santorelli, M Sciacco, K Tanji, et al.Annals of Neurology|June 1, 1996
Familial cerebral cavernous angioma: a gene localized to a 15-cM interval on chromosome 7qA Gil-Nagel, J Dubovsky, K J Wilcox, et al.Annals of Neurology|June 1, 1996
Difficulties in distinguishing sporadic from familial amyotrophic lateral sclerosisR W Orrell, J Habgood, P Rudge, et al.Annals of Neurology|April 1, 1996
Impact of aerobic training on fitness and quality of life in multiple sclerosisJ H Petajan, E Gappmaier, A T White, et al.Annals of Neurology|April 1, 1996
Thalamic metbolism and corticospinal tract integrity determine motor recovery in strokeF Binkofski, R J Seitz, S Arnold, et al.Annals of Neurology|April 1, 1996
Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophyK C Wilhelmsen, D M Blake, T Lynch, et al.Annals of Neurology|May 1, 1996
Brain thiamine, its phosphate esters, and its metabolizing enzymes in Alzheimer's diseaseF Mastrogiacoma, L Bettendorff, T Grisar, et al.Annals of Neurology|May 1, 1996
Brain protein and alpha-ketoglutarate dehydrogenase complex activity in Alzheimer's diseaseF Mastrogiacoma, J G Lindsay, L Bettendorff, et al.Annals of Neurology|May 1, 1996
Paramyotonia congenita: the R1448P Na+ channel mutation in adult human skeletal muscleH Lerche, N Mitrovic, V Dubowitz, et al.Annals of Neurology|May 1, 1996
GTP-cyclohydrolase I gene mutations in hereditary progressive amd dopa-responsive dystoniaY Furukawa, M Shimadzu, A H Rajput, et al.Pageof 982