These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 2396938)

  • 1. 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]  

  • 2. Linkage analysis in spinopontine atrophy: correlation of HLA linkage with phenotypic findings in hereditary ataxia.
    Bale AE; Bale SJ; Schlesinger SL; McFarland HF
    Am J Med Genet; 1987 Jul; 27(3):595-602. PubMed ID: 3477098
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Autopsy cases of hereditary ataxia pathologically diagnosed as the Japanese type of Joseph disease--cliniconeuropathological findings].
    Kogure T; Oda T; Katoh Y
    Seishin Shinkeigaku Zasshi; 1990; 92(3):161-83. PubMed ID: 2353076
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. [Machado-Joseph disease in a family of Spanish origin].
    Pou-Serradell A; Russi A; Ferrer I; Galofré E; Escudero D
    Rev Neurol (Paris); 1987; 143(6-7):520-5. PubMed ID: 3477847
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. [Some problems on the clinical phenotype of Machado-Joseph disease in relation between their ages at onset].
    Iwabuchi K; Kogure T; Oda T; Kato Y; Ohtani K; Endo K; Kosaka K; Amano N; Yagishita S
    No To Shinkei; 1993 Mar; 45(3):246-54. PubMed ID: 8323819
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Type III Machado-Joseph disease in a Japanese family: a clinicopathological study with special reference to the peripheral nervous system.
    Kanda T; Isozaki E; Kato S; Tanabe H; Oda M
    Clin Neuropathol; 1989; 8(3):134-41. PubMed ID: 2743650
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. The Neuropathology of Spinocerebellar Ataxia Type 3/Machado-Joseph Disease.
    Koeppen AH
    Adv Exp Med Biol; 2018; 1049():233-241. PubMed ID: 29427106
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Linkage disequilibrium at the Machado-Joseph disease/spinal cerebellar ataxia 3 locus: evidence for a common founder effect in French and Portuguese-Brazilian families as well as a second ancestral Portuguese-Azorean mutation.
    Stevanin G; Cancel G; Didierjean O; Dürr A; Abbas N; Cassa E; Feingold J; Agid Y; Brice A
    Am J Hum Genet; 1995 Nov; 57(5):1247-50. PubMed ID: 7485178
    [No Abstract]   [Full Text] [Related]  

  • 14. Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype.
    Robitaille Y; Schut L; Kish SJ
    Acta Neuropathol; 1995; 90(6):572-81. PubMed ID: 8615077
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Machado-Joseph disease or not?
    Dawson DM
    Arch Neurol; 1991 Jun; 48(6):570. PubMed ID: 2039375
    [No Abstract]   [Full Text] [Related]  

  • 17. Infantile onset spinocerebellar ataxia with sensory neuropathy (IOSCA): neuropathological features.
    Lönnqvist T; Paetau A; Nikali K; von Boguslawski K; Pihko H
    J Neurol Sci; 1998 Nov; 161(1):57-65. PubMed ID: 9879682
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Clinicopathological study of Joseph disease: report of 4 pedigrees and its nosological consideration].
    Sasaki H; Wakisaka A; Hamada K; Hamada T; Shima K; Tashiro K
    Hokkaido Igaku Zasshi; 1992 Mar; 67(2):174-90. PubMed ID: 1597300
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Machado-Joseph disease is genetically different from Holguin dominant ataxia (SCA2).
    Silveira I; Manaia A; Melki J; Magariño C; Lunkes A; Hernandez A; Gispert S; Burlet P; Rozet JM; Coutinho P
    Genomics; 1993 Sep; 17(3):556-9. PubMed ID: 7902323
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The Machado-Joseph disease locus is different from the spinocerebellar ataxia locus (SCA1).
    Carson WJ; Radvany J; Farrer LA; Vincent D; Rosenberg RN; MacLeod PM; Rouleau GA
    Genomics; 1992 Jul; 13(3):852-5. PubMed ID: 1639414
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.