105 related articles for article (PubMed ID: 2039375)
1. Machado-Joseph disease or not?
Dawson DM
Arch Neurol; 1991 Jun; 48(6):570. PubMed ID: 2039375
[No Abstract] [Full Text] [Related]
2. 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]
3. 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]
4. Machado-Joseph disease, spinopontine atrophy, and SCA3.
Genis D; Volpini V
Neurology; 1997 Apr; 48(4):1137-9. PubMed ID: 9109924
[No Abstract] [Full Text] [Related]
5. Dominantly inherited cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia-I, Machado-Joseph disease, or Dentato-Rubro-Pallido-Luysian atrophy locus.
Subramony SH; Fratkin JD; Manyam BV; Currier RD
Mov Disord; 1996 Mar; 11(2):174-80. PubMed ID: 8684388
[TBL] [Abstract][Full Text] [Related]
6. Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease.
Matilla T; McCall A; Subramony SH; Zoghbi HY
Ann Neurol; 1995 Jul; 38(1):68-72. PubMed ID: 7611728
[TBL] [Abstract][Full Text] [Related]
7. Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease.
Higgins JJ; Nee LE; Vasconcelos O; Ide SE; Lavedan C; Goldfarb LG; Polymeropoulos MH
Neurology; 1996 Jan; 46(1):208-13. PubMed ID: 8559377
[TBL] [Abstract][Full Text] [Related]
8. Machado-Joseph disease mutations as the genetic basis of most spinocerebellar ataxias in Germany.
Schöls L; Amoiridis G; Langkafel M; Büttner T; Przuntek H; Riess O; Vieira-Saecker AM; Epplen JT
J Neurol Neurosurg Psychiatry; 1995 Oct; 59(4):449-50. PubMed ID: 7561932
[No Abstract] [Full Text] [Related]
9. Machado-Joseph disease and SCA3: the genotype meets the phenotypes.
Junck L; Fink JF
Neurology; 1996 Jan; 46(1):4-8. PubMed ID: 8559417
[No Abstract] [Full Text] [Related]
10. Electrophysiological features of central motor conduction in spinocerebellar atrophy type 1, type 2, and Machado-Joseph disease.
Yokota T; Sasaki H; Iwabuchi K; Shiojiri T; Yoshino A; Otagiri A; Inaba A; Yuasa T
J Neurol Neurosurg Psychiatry; 1998 Oct; 65(4):530-4. PubMed ID: 9771779
[TBL] [Abstract][Full Text] [Related]
11. Flattened facial colliculus on magnetic resonance imaging in Machado-Joseph disease.
Ogawa Y; Ito S; Makino T; Kanai K; Arai K; Kuwabara S
Mov Disord; 2012 Jul; 27(8):1041-6. PubMed ID: 22693147
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Spinocerebellar ataxia type 2.
Silverman IE
Arch Neurol; 1999 May; 56(5):628. PubMed ID: 10328260
[No Abstract] [Full Text] [Related]
14. Glutamate dehydrogenase deficiency in Machado-Joseph disease.
Gonçalves A; Oliveira C; Ferro MA; Dinis M; Cunha L
Can J Neurol Sci; 1993 May; 20(2):147-50. PubMed ID: 8334577
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. 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]
17. [An autopsied case of type 2 Machado-Joseph's disease or spino-pontine degeneration].
Iwabuchi K; Nagatomo H; Tanabe T; Sakai H; Yagishita S
No To Shinkei; 1993 Aug; 45(8):733-40. PubMed ID: 8217397
[TBL] [Abstract][Full Text] [Related]
18. Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) families.
Iughetti P; Otto PA; Zatz M; Passos Bueno MR; Marie SK
Am J Med Genet; 1998 May; 77(3):246-8. PubMed ID: 9605593
[No Abstract] [Full Text] [Related]
19. Epidemiology and clinical aspects of Machado-Joseph disease.
Sequeiros J; Coutinho P
Adv Neurol; 1993; 61():139-53. PubMed ID: 8421964
[No Abstract] [Full Text] [Related]
20. [Clinical studies on a large family of probable Machado-Joseph disease in Japan].
Takiyama Y; Tanaka Y; Mizuno Y; Yoshida M
Rinsho Shinkeigaku; 1987 May; 27(5):569-78. PubMed ID: 3476233
[No Abstract] [Full Text] [Related]
[Next] [New Search]