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Journal Abstract Search

89 related items for PubMed ID: 1295057

  • 21.
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  • 22. Sporadic distal myopathy with early adult onset.
    Miller RG, Blank NK, Layzer RB.
    Ann Neurol; 1979 Mar; 5(3):220-7. PubMed ID: 443754
    [Abstract] [Full Text] [Related]

  • 23. Emery-dreifuss humeroperoneal muscular dystrophy: an x-linked myopathy with unusual contractures and bradycardia.
    Hopkins LC, Jackson JA, Elsas LJ.
    Ann Neurol; 1981 Sep; 10(3):230-7. PubMed ID: 7294729
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  • 26. A case of myopathy associated with a dystrophin gene deletion and abnormal glycogen storage.
    Rose MR, Howard RS, Genet SA, McMahon CJ, Whitfield A, Morgan-Hughes JA.
    Muscle Nerve; 1993 Jan; 16(1):57-62. PubMed ID: 8423832
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  • 27. [Late centronuclear myopathy: autosomal dominant form].
    Cartier L, Hernández JE.
    Rev Med Chil; 1996 Feb; 124(2):209-16. PubMed ID: 9213890
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  • 28. Adult course in dynamin 2 dominant centronuclear myopathy with neonatal onset.
    Melberg A, Kretz C, Kalimo H, Wallgren-Pettersson C, Toussaint A, Böhm J, Stålberg E, Laporte J.
    Neuromuscul Disord; 2010 Jan; 20(1):53-6. PubMed ID: 19932619
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  • 30. [Distal myopathy].
    Badurska B, Pfeffer-Baczuk A.
    Neurol Neurochir Pol; 1985 Jan; 19(6):512-5. PubMed ID: 3835492
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  • 35. [Familial myopathy with exclusively cardiac clinical expression].
    Morand P, Bienvenu P, Daumas PL, Kieffer A, Muh JP, Raynaud R.
    Arch Mal Coeur Vaiss; 1977 Oct; 70(10):1097-103. PubMed ID: 413519
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  • 36. Centronuclear myopathy: possible central nervous system origin.
    Serratrice G, Pellissier JF, Faugere MC, Gastaut JL.
    Muscle Nerve; 1978 Oct; 1(1):62-9. PubMed ID: 752109
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  • 37. A distinct phenotype of distal myopathy in a large Finnish family.
    Mahjneh I, Haravuori H, Paetau A, Anderson LV, Saarinen A, Udd B, Somer H.
    Neurology; 2003 Jul 08; 61(1):87-92. PubMed ID: 12847162
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  • 38. Infantile autosomal dominant distal myopathy.
    Scoppetta C, Casali C, La Cesa I, Sermoni A, Mercuri B, Pierelli F, Vaccario ML.
    Acta Neurol Scand; 1995 Aug 08; 92(2):122-6. PubMed ID: 7484058
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  • 39. Benign muscular dystrophy with autosomal dominant inheritance.
    Somer H, Laulumaa V, Paljärvi L, Partanen J, Lamminen A, Pihko H, Sariola H, Haltia M.
    Neuromuscul Disord; 1991 Aug 08; 1(4):267-73. PubMed ID: 1822805
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  • 40. Genetics of congenital nemaline myopathy: a study of 10 families.
    Wallgren-Pettersson C, Kääriäinen H, Rapola J, Salmi T, Jääskeläinen J, Donner M.
    J Med Genet; 1990 Aug 08; 27(8):480-7. PubMed ID: 2213842
    [Abstract] [Full Text] [Related]

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