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Journal Abstract Search

79 related items for PubMed ID: 6661874

  • 1. [Familial occurrence of Fukuyama type congenital muscular dystrophy and limb-girdle syndrome].
    Riku S, Kumagai T, Sobue I.
    Rinsho Shinkeigaku; 1983 Aug; 23(8):711-6. PubMed ID: 6661874
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  • 4. The congenital and limb-girdle muscular dystrophies: sharpening the focus, blurring the boundaries.
    Kirschner J, Bönnemann CG.
    Arch Neurol; 2004 Feb; 61(2):189-99. PubMed ID: 14967765
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  • 6. Spinal reflex activity in patients with Duchenne, Limb-Girdle and myotonic muscular dystrophies.
    Sica RE, Rey RC.
    Medicina (B Aires); 1985 Feb; 45(5):501-7. PubMed ID: 3842457
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  • 7. [Updates in muscular dystrophies].
    Erazo-Torricelli R.
    Rev Neurol; 1985 Feb; 39(9):860-71. PubMed ID: 15543503
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  • 8. [Limb-girdle syndrome. A study of 46 cases].
    Ferrer X, Larrivière M, Coquet M, Ellie E, Lagueny A, Julien J.
    Rev Neurol (Paris); 1993 Feb; 149(12):788-93. PubMed ID: 7997739
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  • 9. Cerebro-oculo-muscular syndrome: a variant of Fukuyama congenital cerebromuscular dystrophy.
    Dambska M, Wisniewski K, Sher J, Solish G.
    Clin Neuropathol; 1982 Feb; 1(3):93-8. PubMed ID: 6820333
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  • 10. [Unusual sibling cases of Fukuyama type congenital muscular dystrophy (author's transl)].
    Riku S, Konagaya M, Ibi T, Sobue I.
    Rinsho Shinkeigaku; 1982 Mar; 22(3):216-22. PubMed ID: 7105594
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  • 11. [Fukuyama type congenital muscular dystrophy].
    Osawa M, Hino N.
    Ryoikibetsu Shokogun Shirizu; 2001 Mar; (35):97-102. PubMed ID: 11556002
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  • 13. [Fukuyama congenital muscular dystrophy and related alpha-dystroglycanopathies].
    Murakami T, Nishino I.
    Brain Nerve; 2008 Oct; 60(10):1159-64. PubMed ID: 18975603
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  • 14. [Staircase phenomenon in "mitochodrial myopathy' and limb-girdle type muscular dystrophy].
    Sunohara N, Tomi H, Tachibana S, Nonaka I, Satoyoshi E.
    Rinsho Shinkeigaku; 1982 Sep; 22(9):799-809. PubMed ID: 7160127
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  • 15. Limb girdle muscular dystrophy: description of a phenotype.
    Stübgen JP.
    Muscle Nerve; 1994 Dec; 17(12):1449-55. PubMed ID: 7969245
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  • 17. A case of Fukuyama-type congenital muscular dystrophy with a very mild mental deficit.
    Hino-Fukuyo N, Haginoya K, Hayashi YK, Nishino I, Murakami T, Nonaka I, Togashi K, Tanaka S, Takayanagi M, Yokoyama H, Sakamoto O, Abe T, Toda T, Iinuma K.
    Neuromuscul Disord; 2006 Apr; 16(4):274-6. PubMed ID: 16545565
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  • 18. [Update on diagnosis of limb girdle muscular dystrophy].
    Nevo Y, Yaron Y.
    Harefuah; 1999 May 02; 136(9):720-5. PubMed ID: 10955098
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  • 19. Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-alpha 2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?
    Taniguchi M, Kurahashi H, Noguchi S, Sese J, Okinaga T, Tsukahara T, Guicheney P, Ozono K, Nishino I, Morishita S, Toda T.
    Biochem Biophys Res Commun; 2006 Apr 07; 342(2):489-502. PubMed ID: 16487936
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  • 20. Differential diagnosis of limb girdle syndromes.
    Ishpekova B, Milanov I.
    Electromyogr Clin Neurophysiol; 1996 Dec 07; 36(8):469-75. PubMed ID: 8985674
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