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Journal Abstract Search

288 related items for PubMed ID: 7254232

  • 21. [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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  • 22. [An autopsy case with lower motor neuron disease showing a transient-appearance of anti-GM1 antibody and an improvement of conduction block after gamma-globulin administration].
    Kikuchi H, Kawano Y, Dohura K, Kawamura T, Taniwaki T, Yamada T, Kato M, Iwaki T, Kira J.
    No To Shinkei; 1999 May; 51(5):455-64. PubMed ID: 10396755
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  • 23. [2 autopsy cases of congenital muscular dystrophy of Fukuyama type--a typical and an atypical cases].
    Koga M, Abe M, Tateishi J, Antoku Y, Iwashita H, Miyoshino S.
    No To Shinkei; 1984 Nov; 36(11):1103-8. PubMed ID: 6525323
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  • 24. Oculopharyngeal muscular dystrophy: non-French-Canadian pedigrees.
    Creel GB, Giuliani MJ, Lacomis D, Holbach SM.
    Muscle Nerve; 1998 Jun; 21(6):816-8. PubMed ID: 9585341
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  • 30. Oculopharyngeal muscular dystrophy and mitochondrial abnormalities.
    Arenas J, Huertas RA, Campos Y, Cabello A, Gutierrez E, Bautista J, Segura D.
    Muscle Nerve; 1992 Sep; 15(9):1055-6. PubMed ID: 1518515
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  • 32. Oculopharyngeal muscular dystrophy: clinical and morphological follow-up study reveals mitochondrial alterations and unique nuclear inclusions in a severe autosomal recessive type.
    Schröder JM, Krabbe B, Weis J.
    Neuropathol Appl Neurobiol; 1995 Feb; 21(1):68-73. PubMed ID: 7770123
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  • 34. [Oculopharyngeal muscular dystrophy with dysphagia in a Jewess from Uzbekistan].
    Ben Simon G, Felberg I, Sadeh M, Farfel Z.
    Harefuah; 1995 Feb 15; 128(4):220-1, 263. PubMed ID: 7744330
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  • 36. Mitochondrial abnormalities in oculopharyngeal muscular dystrophy.
    Sadeh M, Pauzner R, Blatt I, Mouallem M, Farfel Z.
    Muscle Nerve; 1993 Sep 15; 16(9):982-3. PubMed ID: 8257512
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  • 37. Intranuclear inclusions in oculopharyngeal muscular dystrophy among Bukhara Jews.
    Blumen SC, Sadeh M, Korczyn AD, Rouche A, Nisipeanu P, Asherov A, Tomé FM.
    Neurology; 1996 May 15; 46(5):1324-8. PubMed ID: 8628475
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  • 39. 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 15; 46(3):773-8. PubMed ID: 8618681
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