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Journal Abstract Search

106 related items for PubMed ID: 3347807

  • 21. Characteristic clinical findings in some neurogenic myopathies and in some myogenic myopathies causing muscular weakness, hypotonia and atrophy in infancy and early childhood.
    Gamstorp I.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):72-81. PubMed ID: 5173129
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  • 23. Distal muscular dystrophy. Case reports.
    Ishpekova B, Milanov I.
    Electromyogr Clin Neurophysiol; 1997 Feb; 37(4):201-5. PubMed ID: 9208214
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  • 24. Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy.
    Baker NL, Mörgelin M, Peat R, Goemans N, North KN, Bateman JF, Lamandé SR.
    Hum Mol Genet; 2005 Jan 15; 14(2):279-93. PubMed ID: 15563506
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  • 25. Adult onset limb-girdle muscular dystrophy with autosomal dominant inheritance.
    Somer H, Laulumaa V, Paljärvi L, Partanen J, Haltia M.
    Prog Clin Biol Res; 1989 Jan 15; 306():69-71. PubMed ID: 2740412
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  • 28. Slowly progressive proximal weakness: limb-girdle syndromes.
    Fowler WM, Nayak NN.
    Arch Phys Med Rehabil; 1983 Nov 15; 64(11):527-38. PubMed ID: 6357144
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  • 29. Early-onset benign autosomal-dominant limb-girdle myopathy with contractures (Bethlem myopathy).
    Tachi N, Tachi M, Sasaki K, Imamura S.
    Pediatr Neurol; 1989 Nov 15; 5(4):232-6. PubMed ID: 2803379
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  • 31. [Familial scapuloperoneal-type myopathy associated with a marked elevation of serum creatine kinase and hepatomegaly].
    Maruoka A, Ideguchi H, Nawata H, Goto I, Ibayashi H.
    Rinsho Shinkeigaku; 1989 Mar 15; 29(3):325-31. PubMed ID: 2752661
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  • 33. Benign congenital muscular dystrophy with autosomal dominant heredity: problems of classification.
    Schmalbruch H, Kamieniecka Z, Fuglsang-Frederiksen A, Trojaborg W.
    J Neurol; 1987 Apr 15; 234(3):146-51. PubMed ID: 3585421
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  • 36. 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 Apr 15; 1(4):267-73. PubMed ID: 1822805
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  • 40. Autosomal dominant limb-girdle muscular dystrophy with ankle joint contracture.
    Tanaka K, Yamada T, Kikuchi H, Mitsunaga Y, Furuya H, Kira J.
    Acta Neurol Scand; 1999 Sep 15; 100(3):199-201. PubMed ID: 10478586
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