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Journal Abstract Search

139 related items for PubMed ID: 1914322

  • 1. [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
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  • 2. [A family with oculopharyngeal muscular dystrophy with (GCG)9 expansion in which a sister had neck as well as proximal and her brother proximal lower limb muscle weakness].
    Takahashi T, Tateyama M, Aoki M, Shiga Y, Uyama E, Itoyama Y.
    Rinsho Shinkeigaku; 2000 Sep; 40(9):911-4. PubMed ID: 11257788
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  • 3. [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
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  • 4. [Oculopharyngeal muscular dystrophy in a Japanese family].
    Tokunaga M, Uyama E, Tooya M, Kumamoto T, Araki S.
    Rinsho Shinkeigaku; 1990 Jan; 30(1):29-36. PubMed ID: 2184963
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  • 5. [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
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  • 12. Oculopharyngeal muscular dystrophy.
    Brais B, Rouleau GA, Bouchard JP, Fardeau M, Tomé FM.
    Semin Neurol; 1999 May; 19(1):59-66. PubMed ID: 10711989
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  • 13. [A family of autosomal dominant facio-limb-girdle muscular dystrophy].
    Takao S, Kira J, Kohtake N, Yoshimura T, Goto I.
    Fukuoka Igaku Zasshi; 1996 Dec; 87(12):278-82. PubMed ID: 9011111
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  • 14. Distal muscular dystrophy of the Miyoshi type.
    Yildiz H, Emre U, Coskun O, Ergün U, Atasoy HT, Inan LE.
    Clin Neuropathol; 2003 Dec; 22(4):204-8. PubMed ID: 12908758
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