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Journal Abstract Search

165 related items for PubMed ID: 13469173

  • 41. [Pseudohypertrophic proximal progressive muscular dystrophy with a malignant course manifesting itself in adolescence].
    Badalian LO, Temin PA, Saidbegov DG, Nikitin MV, Arkhipov BA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1989; 89(3):113-20. PubMed ID: 2728733
    [Abstract] [Full Text] [Related]

  • 42. The incidence and heredity of muscular dystrophy; a study of 71 patients admitted to the Massachusetts General Hospital.
    BROWN MR.
    N Engl J Med; 1951 Jan 18; 244(3):88-90. PubMed ID: 14796792
    [No Abstract] [Full Text] [Related]

  • 43. Muscular dystrophy.
    Arahata K.
    Neuropathology; 2000 Sep 18; 20 Suppl():S34-41. PubMed ID: 11037185
    [Abstract] [Full Text] [Related]

  • 44. [Humeral-peroneal muscular dystrophy with cardiomyopathy and sex-linked recessive heredity (Emery-Dreifuss). Description of a case with orthopedic problems].
    Merlini L, Granata C, Bonfiglioli S, Mattutini P.
    Chir Organi Mov; 1984 Sep 18; 69(3):291-5. PubMed ID: 6398205
    [No Abstract] [Full Text] [Related]

  • 45. [2 families with benign myopathy predominantly on the limb girdle with dominant autosomal heredity].
    Serratrice G, Pellissier JF.
    Rev Neurol (Paris); 1988 Sep 18; 144(1):43-6. PubMed ID: 3347807
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  • 46. Linkage analyses in tibial muscular dystrophy.
    Nokelainen P, Udd B, Somer H, Peltonen L.
    Hum Hered; 1996 Sep 18; 46(2):98-107. PubMed ID: 8666419
    [Abstract] [Full Text] [Related]

  • 47. Early onset muscular dystrophy with autosomal dominant heredity. Report of a family and CT findings of skeletal muscle.
    Tohyama J, Inagaki M, Nonaka I.
    Brain Dev; 1994 Sep 18; 16(5):402-6. PubMed ID: 7892962
    [Abstract] [Full Text] [Related]

  • 48. NEUROLOGICAL clinical pathological conference: progressive muscular dystrophy.
    Dis Nerv Syst; 1953 Jun 18; 14(6):183-90. PubMed ID: 13052050
    [No Abstract] [Full Text] [Related]

  • 49. Autosomal recessive oculopharyngeal muscular dystrophy.
    Fried K, Arlozorov A, Spira R.
    J Med Genet; 1975 Dec 18; 12(4):416-8. PubMed ID: 1219124
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  • 55. Landouzy-Dejerine disease: a progressive metameric muscular dystrophy of autosomal dominant inheritance with a variable intrafamilial phenotype expression.
    Rossi A, Giannini F, D'Amore I, Guazzi GC.
    Acta Neurol (Napoli); 1985 Apr 18; 7(2):93-111. PubMed ID: 4013841
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  • 57. Zebrafish orthologs of human muscular dystrophy genes.
    Steffen LS, Guyon JR, Vogel ED, Beltre R, Pusack TJ, Zhou Y, Zon LI, Kunkel LM.
    BMC Genomics; 2007 Mar 20; 8():79. PubMed ID: 17374169
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