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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

233 related items for PubMed ID: 1620135

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. [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
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. [Linkage study of hereditary spinocerebellar ataxia, and probable correlation for the loci to the disease phenotypes].
    Sasaki H.
    Rinsho Shinkeigaku; 1993 Dec; 33(12):1285-7. PubMed ID: 8174326
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No 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
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. [Cumulative familial olivopontocerebellar atrophy type IV].
    Erös E, Czeizel E.
    Orv Hetil; 1994 Apr 10; 135(15):801-4. PubMed ID: 8177597
    [Abstract] [Full Text] [Related]

  • 14. Joseph's disease: an autosomal dominant neurological disease in the Portuguese of the United States and the Azores Islands.
    Rosenberg RN, Nyhan WL, Coutinho P, Bay C.
    Adv Neurol; 1978 Apr 10; 21():33-57. PubMed ID: 735930
    [Abstract] [Full Text] [Related]

  • 15. Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature.
    Pascual-Castroviejo I, Gutierrez M, Morales C, Gonzalez-Mediero I, Martínez-Bermejo A, Pascual-Pascual SI.
    Neuropediatrics; 1994 Aug 10; 25(4):183-90. PubMed ID: 7824090
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. 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 Aug 10; 8(3):134-41. PubMed ID: 2743650
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Dominantly inherited hypoplasia of the vermis.
    Rivier F, Echenne B.
    Neuropediatrics; 1992 Aug 10; 23(4):206-8. PubMed ID: 1407388
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.