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22. Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and spinocerebellar ataxia type 1. Hashida H; Goto J; Kurisaki H; Mizusawa H; Kanazawa I Ann Neurol; 1997 Apr; 41(4):505-11. PubMed ID: 9124808 [TBL] [Abstract][Full Text] [Related]
23. Somatic mosaicism in the central nervous system in spinocerebellar ataxia type 1 and Machado-Joseph disease. Lopes-Cendes I; Maciel P; Kish S; Gaspar C; Robitaille Y; Clark HB; Koeppen AH; Nance M; Schut L; Silveira I; Coutinho P; Sequeiros J; Rouleau GA Ann Neurol; 1996 Aug; 40(2):199-206. PubMed ID: 8773601 [TBL] [Abstract][Full Text] [Related]
24. Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients. Silveira I; Lopes-Cendes I; Kish S; Maciel P; Gaspar C; Coutinho P; Botez MI; Teive H; Arruda W; Steiner CE; Pinto-Júnior W; Maciel JA; Jerin S; Sack G; Andermann E; Sudarsky L; Rosenberg R; MacLeod P; Chitayat D; Babul R; Sequeiros J; Rouleau GA Neurology; 1996 Jan; 46(1):214-8. PubMed ID: 8559378 [TBL] [Abstract][Full Text] [Related]
25. Abnormalities of mitochondrial enzymes in hereditary ataxias. Sorbi S; Piacentini S; Fani C; Tonini S; Marini P; Amaducci L Acta Neurol Scand; 1989 Aug; 80(2):103-10. PubMed ID: 2816270 [TBL] [Abstract][Full Text] [Related]
26. Machado Joseph disease is not an allele of the spinocerebellar ataxia 2 locus. Twist EC; Farrer LA; Macleod PM; Radvany J; Chamberlain S; Rosenberg RN; Rouleau GA Hum Genet; 1994 Mar; 93(3):335-8. PubMed ID: 8125487 [TBL] [Abstract][Full Text] [Related]
27. Detection of the Machado-Joseph disease/spinocerebellar ataxia three trinucleotide repeat expansion in families with autosomal dominant motor disorders, including the Drew family of Walworth. Giunti P; Sweeney MG; Harding AE Brain; 1995 Oct; 118 ( Pt 5)():1077-85. PubMed ID: 7496771 [TBL] [Abstract][Full Text] [Related]
28. Glutamate dehydrogenase and aspartate aminotransferase in leukocytes of patients with motor neuron disease. Hugon J; Tabaraud F; Rigaud M; Vallat JM; Dumas M Neurology; 1989 Jul; 39(7):956-8. PubMed ID: 2739923 [TBL] [Abstract][Full Text] [Related]
29. Frequency of the different mutations causing spinocerebellar ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a large group of Brazilian patients. Lopes-Cendes I; Teive HG; Calcagnotto ME; Da Costa JC; Cardoso F; Viana E; Maciel JA; Radvany J; Arruda WO; Trevisol-Bittencourt PC; Rosa Neto P; Silveira I; Steiner CE; Pinto Júnior W; Santos AS; Correa Neto Y; Werneck LC; Araújo AQ; Carakushansky G; Mello LR; Jardim LB; Rouleau GA Arq Neuropsiquiatr; 1997 Sep; 55(3B):519-29. PubMed ID: 9629399 [TBL] [Abstract][Full Text] [Related]
30. Leukocyte glutamate dehydrogenase and CSF amino acids in late onset ataxias. Kaakkola S; Marnela KM; Oja SS; Icén A; Palo J Acta Neurol Scand; 1990 Nov; 82(5):292-6. PubMed ID: 2281745 [TBL] [Abstract][Full Text] [Related]
31. Spinocerebellar ataxia, type 3 (SCA3) is genetically identical to Machado-Joseph disease (MJD). Haberhausen G; Damian MS; Leweke F; Müller U J Neurol Sci; 1995 Sep; 132(1):71-5. PubMed ID: 8523034 [TBL] [Abstract][Full Text] [Related]
32. [Molecular and clinical features in spinocerebellar ataxia type 6 (SCA6) in Japanese]. Ikeuchi T Nihon Rinsho; 1999 Apr; 57(4):891-5. PubMed ID: 10222785 [TBL] [Abstract][Full Text] [Related]
33. Machado-Joseph disease in New England: clinical description and distinction from the olivopontocerebellar atrophies. Sudarsky L; Corwin L; Dawson DM Mov Disord; 1992; 7(3):204-8. PubMed ID: 1620136 [TBL] [Abstract][Full Text] [Related]
34. [Overview of Hereditary Spinocerebellar Ataxias in Japan]. Tada M; Yokoseki A; Onodera O Brain Nerve; 2017 Aug; 69(8):879-890. PubMed ID: 28819072 [TBL] [Abstract][Full Text] [Related]
35. Family with dominantly inherited ataxia, amyotrophy, and peripheral sensory loss. Spinopontine atrophy or Machado-Joseph Azorean disease in another non-Portuguese family? Eto K; Sumi SM; Bird TD; McEvoy-Bush T; Boehnke M; Schellenberg G Arch Neurol; 1990 Sep; 47(9):968-74. PubMed ID: 2396938 [TBL] [Abstract][Full Text] [Related]
36. Nine families with the SCA3/Machado-Joseph disease type of inherited ataxia. Greenstein PE; Moore D; Levy-Lohad E; Stephens K; Bird TD Neurology; 1996 Oct; 47(4):1106-7. PubMed ID: 8857759 [No Abstract] [Full Text] [Related]
37. [Molecular genetics of hereditary spinocerebellar ataxia]. Tsuji S No To Shinkei; 1995 Oct; 47(10):955-61. PubMed ID: 7577140 [No Abstract] [Full Text] [Related]
38. Sequence variation and size ranges of CAG repeats in the Machado-Joseph disease, spinocerebellar ataxia type 1 and androgen receptor genes. Rubinsztein DC; Leggo J; Coetzee GA; Irvine RA; Buckley M; Ferguson-Smith MA Hum Mol Genet; 1995 Sep; 4(9):1585-90. PubMed ID: 8541843 [TBL] [Abstract][Full Text] [Related]
39. Frequency analysis of autosomal dominant cerebellar ataxias in Japanese patients and clinical characterization of spinocerebellar ataxia type 6. Watanabe H; Tanaka F; Matsumoto M; Doyu M; Ando T; Mitsuma T; Sobue G Clin Genet; 1998 Jan; 53(1):13-9. PubMed ID: 9550356 [TBL] [Abstract][Full Text] [Related]
40. Glutamate and pyruvate dehydrogenase deficiency in spinocerebellar degeneration. Maruyama S; Yamaguchi T Adv Neurol; 1984; 41():255-65. PubMed ID: 6437168 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]