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Journal Abstract Search

268 related items for PubMed ID: 9296168

  • 1. [Mitochondrial anomalies in oculopharyngeal muscular dystrophy].
    de Seze J, Pasquier F, Ruchoux MM, Hurtevent JF, Petit H.
    Rev Neurol (Paris); 1997 Jun; 153(5):335-8. PubMed ID: 9296168
    [Abstract] [Full Text] [Related]

  • 2. Mitochondrial abnormalities in oculopharyngeal muscular dystrophy.
    Pauzner R, Blatt I, Mouallem M, Ben-David E, Farfel Z, Sadeh M.
    Muscle Nerve; 1991 Oct; 14(10):947-52. PubMed ID: 1944407
    [Abstract] [Full Text] [Related]

  • 3. Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the disease.
    Blumen SC, Brais B, Korczyn AD, Medinsky S, Chapman J, Asherov A, Nisipeanu P, Codère F, Bouchard JP, Fardeau M, Tomé FM, Rouleau GA.
    Ann Neurol; 1999 Jul; 46(1):115-8. PubMed ID: 10401788
    [Abstract] [Full Text] [Related]

  • 4. [A Japanese pedigree with oculopharyngeal muscular dystrophy].
    Nohira O, Imai N, Okabe T, Hamaguchi K.
    Rinsho Shinkeigaku; 1994 May; 34(5):461-5. PubMed ID: 7924058
    [Abstract] [Full Text] [Related]

  • 5. A rapidly progressive adolescent-onset oculopharyngeal somatic syndrome with rimmed vacuoles in two siblings.
    Rose MR, Landon DN, Papadimitriou A, Morgan-Hughes JA.
    Ann Neurol; 1997 Jan; 41(1):25-31. PubMed ID: 9005862
    [Abstract] [Full Text] [Related]

  • 6. Oculopharyngeal muscular dystrophy.
    Adamczyk DT, Oshinskie L.
    J Am Optom Assoc; 1987 May; 58(5):408-12. PubMed ID: 3584810
    [Abstract] [Full Text] [Related]

  • 7. Morphological changes in muscle fibers in oculopharyngeal muscular dystrophy.
    Tomé FM, Chateau D, Helbling-Leclerc A, Fardeau M.
    Neuromuscul Disord; 1997 Oct; 7 Suppl 1():S63-9. PubMed ID: 9392019
    [Abstract] [Full Text] [Related]

  • 8. Ocular myopathies.
    Tomé FM, Fardeau M.
    Pathol Res Pract; 1985 Jul; 180(1):19-27. PubMed ID: 4034429
    [Abstract] [Full Text] [Related]

  • 9. [Autosomal recessive oculopharyngeal "muscular dystrophy"--clinical features and association with reduced activity of myophosphorylase].
    Nishimura M, Miyamoto K, Motoyoshi Y, Sugie H, Tanabe H.
    Rinsho Shinkeigaku; 1991 Apr; 31(4):383-90. PubMed ID: 1914322
    [Abstract] [Full Text] [Related]

  • 10. Oculopharyngeal muscular dystrophy in Italy.
    Meola G, Sansone V, Rotondo G, Tomé FM, Bouchard JP.
    Neuromuscul Disord; 1997 Oct; 7 Suppl 1():S53-6. PubMed ID: 9392017
    [Abstract] [Full Text] [Related]

  • 11. Oculopharyngeal muscular dystrophy in France.
    Fardeau M, Tomé FM.
    Neuromuscul Disord; 1997 Oct; 7 Suppl 1():S30-3. PubMed ID: 9392012
    [Abstract] [Full Text] [Related]

  • 12. [Oculopharyngeal muscular dystrophy].
    Knoblauch A, Köppel M.
    Schweiz Med Wochenschr; 1984 Apr 21; 114(16):557-61. PubMed ID: 6474119
    [Abstract] [Full Text] [Related]

  • 13. Oculopharyngeal muscular dystrophy in two unrelated Japanese families.
    Uyama E, Nohira O, Chateau D, Tokunaga M, Uchino M, Okabe T, Ando M, Tome FM.
    Neurology; 1996 Mar 21; 46(3):773-8. PubMed ID: 8618681
    [Abstract] [Full Text] [Related]

  • 14. [Oculopharyngeal muscular dystrophy].
    Tamir G, Hauben D.
    Harefuah; 1990 Jun 01; 118(11):634-6. PubMed ID: 2387559
    [Abstract] [Full Text] [Related]

  • 15. An autopsy study of a familial oculopharyngeal muscular dystrophy (OPMD) with distal spread and neurogenic involvement.
    Schmitt HP, Krause KH.
    Muscle Nerve; 1981 Jun 01; 4(4):296-305. PubMed ID: 7254232
    [Abstract] [Full Text] [Related]

  • 16. [Oculopharyngeal muscular dystrophy in a Japanese family].
    Tokunaga M, Uyama E, Tooya M, Kumamoto T, Araki S.
    Rinsho Shinkeigaku; 1990 Jan 01; 30(1):29-36. PubMed ID: 2184963
    [Abstract] [Full Text] [Related]

  • 17. An unusual case of muscular limb-girdle dystrophy and mitochondrial myopathy.
    Calore EE, Cavaliere MJ, Wakamatsu A, Perez NM, Maeda MY, Russo DH.
    Pathologica; 1994 Dec 01; 86(6):649-51. PubMed ID: 7617396
    [Abstract] [Full Text] [Related]

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