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Annals of Neurology|March 1, 1995
A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19pK Vahedi, A Joutel, P Van Bogaert, et al.Annals of Neurology|March 1, 1995
In vitro evidence for a dual role of tumor necrosis factor-alpha in human immunodeficiency virus type 1 encephalopathyS G Wilt, E Milward, J M Zhou, et al.Annals of Neurology|March 1, 1995
JC virus DNA in cerebrospinal fluid of human immunodeficiency virus-infected patients: predictive value for progressive multifocal leukoencephalopathyD McGuire, S Barhite, H Hollander, et al.Annals of Neurology|March 1, 1995
An allelic association study of monoamine oxidase B in Parkinson's diseaseS L Ho, A L Kapadi, D B Ramsden, et al.Annals of Neurology|March 1, 1995
The gene for hereditary progressive dystonia with marked diurnal fluctuation maps to chromosome 14qH Tanaka, K Endo, S Tsuji, et al.Annals of Neurology|March 1, 1995
Hyperkalemic periodic paralysis with cardiac dysrhythmia: a novel sodium channel mutation?J L Baquero, R A Ayala, J Wang, et al.Annals of Neurology|September 1, 1995
A Greek-American kindred with autosomal dominant, levodopa-responsive parkinsonism and anticipationK Markopoulou, Z K Wszolek, R F PfeifferAnnals of Neurology|September 1, 1995
Enhanced endothelial cell adhesion of human cerebrospinal fluid lymphocytesR M Elfont, D E Griffin, G W GoldsteinAnnals of Neurology|September 1, 1995
Apolipoprotein E epsilon 4 allele is not associated with earlier age at onset in amyotrophic lateral sclerosisS Mui, G W Rebeck, D McKenna-Yasek, et al.Annals of Neurology|October 1, 1993
beta-Amyloid precursor epitopes in muscle fibers of inclusion body myositisV Askanas, R B Alvarez, W K EngelPageof 982