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Journal Abstract Search

131 related items for PubMed ID: 6859110

  • 1. Oculogastrointestinal muscular dystrophy.
    Ionasescu V.
    Am J Med Genet; 1983 May; 15(1):103-12. PubMed ID: 6859110
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  • 2.
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  • 3. 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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  • 4. A familial visceral myopathy with external ophthalmoplegia and autosomal recessive transmission.
    Anuras S, Mitros FA, Nowak TV, Ionasescu VV, Gurll NJ, Christensen J, Green JB.
    Gastroenterology; 1983 Feb; 84(2):346-53. PubMed ID: 6687359
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  • 5. Oculopharyngodistal myopathy.
    Satoyoshi E, Kinoshita M.
    Arch Neurol; 1977 Feb; 34(2):89-92. PubMed ID: 836191
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  • 6. [A pedigree of autosomal dominant limb-girdle myopathy with rimmed vacuole formation].
    Kishibayashi J, Sunohara N, Saito Y.
    Rinsho Shinkeigaku; 1997 Jul; 37(7):603-10. PubMed ID: 9396357
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  • 10. Hereditary ptosis.
    Aberfeld DC.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):63-5. PubMed ID: 5173128
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  • 11. [Clinicopathological study of a case of oculopharyngeal muscular dystrophy].
    Moreno Martínez JM, Martín Araguz A, García de la Rocha ML, Masjuán Vallejo J, Barón Rubio M, Ginel Feito MD.
    Arch Neurobiol (Madr); 1991 Feb; 54(5):229-32. PubMed ID: 1804038
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  • 12. Neuropathic findings in oculopharyngeal muscular dystrophy. A report of seven cases and a review of the literature.
    Hardiman O, Halperin JJ, Farrell MA, Shapiro BE, Wray SH, Brown RH.
    Arch Neurol; 1993 May; 50(5):481-8. PubMed ID: 8387769
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  • 13. Familial visceral neuropathy as part of a diffuse neuronal syndrome: four fatal cases in one sibship.
    Matulis SR, McJunkin B, Chang HH.
    Am J Gastroenterol; 1994 May; 89(5):792-6. PubMed ID: 8172158
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  • 15. Girls with muscular dystrophy.
    Reddy BK, Kumari CK, Reddy MV, Reddi OS.
    Acta Anthropogenet; 1984 May; 8(3-4):209-16. PubMed ID: 6545753
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  • 16. An autopsy study of a familial oculopharyngeal muscular dystrophy (OPMD) with distal spread and neurogenic involvement.
    Schmitt HP, Krause KH.
    Muscle Nerve; 1981 May; 4(4):296-305. PubMed ID: 7254232
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  • 17. Distal anterior compartment myopathy: a dysferlin mutation causing a new muscular dystrophy phenotype.
    Illa I, Serrano-Munuera C, Gallardo E, Lasa A, Rojas-García R, Palmer J, Gallano P, Baiget M, Matsuda C, Brown RH.
    Ann Neurol; 2001 Jan; 49(1):130-4. PubMed ID: 11198284
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  • 18. Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency.
    Romero NB, Tomé FM, Leturcq F, el Kerch FE, Azibi K, Bachner L, Anderson RD, Roberds SL, Campbell KP, Fardeau M.
    C R Acad Sci III; 1994 Jan; 317(1):70-6. PubMed ID: 7987694
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  • 19. [A case of distal muscular dystrophy (Miyoshi), characterized by early involvement in paravertebral muscle and atypical changes in muscle biopsy specimen].
    Kamakura K, Shimomura S, Higuchi I, Takatani O.
    Rinsho Shinkeigaku; 1988 Jun; 28(6):665-9. PubMed ID: 3233839
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  • 20. Surgery for progressive familial myopathic ptosis.
    Fox SA.
    Ann Ophthalmol; 1971 Sep; 3(9):1033-8. PubMed ID: 5163784
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