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Pubmed for Handhelds

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Journal Abstract Search

269 related items for PubMed ID: 6720743

  • 1. Oculopharyngeal and distal myopathy: a case study from Papua New Guinea.
    Scrimgeour EM, Mastaglia FL.
    Am J Med Genet; 1984 Apr; 17(4):763-71. PubMed ID: 6720743
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  • 5. Oculopharyngeal myopathy with sensorineural hearing loss.
    Alusi GH, Grant WE, Quiney RE.
    J Laryngol Otol; 1996 Jun; 110(6):567-9. PubMed ID: 8763380
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  • 6. Hereditary dysphagia: the oculopharyngeal syndrome.
    Ford LH, Holinger PH.
    Laryngoscope; 1971 Mar; 81(3):373-8. PubMed ID: 5553785
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  • 8. [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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  • 11. Oculopharyngeal muscular dystrophy in Norway. Survey of a large Norwegian family.
    Salvesen R, Brautaset NJ.
    Acta Neurol Scand; 1996 Apr; 93(4):281-5. PubMed ID: 8739439
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  • 16. [From gene to disease; the PABN1 gene and oculopharyngeal muscular dystrophy].
    Schreuder AH, de Die-Smulders CE, Herbergs J, Koehler PJ.
    Ned Tijdschr Geneeskd; 2006 May 20; 150(20):1124-6. PubMed ID: 16756225
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  • 17. [Oculopharyngeal muscular dystrophy].
    Tamir G, Hauben D.
    Harefuah; 1990 Jun 01; 118(11):634-6. PubMed ID: 2387559
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  • 19. Oculopharyngeal muscular dystrophy.
    Adamczyk DT, Oshinskie L.
    J Am Optom Assoc; 1987 May 01; 58(5):408-12. PubMed ID: 3584810
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