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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

156 related items for PubMed ID: 8930416

  • 1.
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  • 2. Neuroimaging manifestations and classification of congenital muscular dystrophies.
    Barkovich AJ.
    AJNR Am J Neuroradiol; 1998 Sep; 19(8):1389-96. PubMed ID: 9763366
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  • 5. Congenital muscular dystrophy, brain and eye abnormalities: one or more clinical entities?
    Laverda AM, Battaglia MA, Drigo P, Battistella PA, Casara GL, Suppiej A, Casellato R.
    Childs Nerv Syst; 1993 Apr; 9(2):84-7. PubMed ID: 8319237
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  • 7. Congenital muscular dystrophy with cerebral and ocular malformations (cerebro-oculo-muscular syndrome).
    Heyer R, Ehrich J, Goebel HH, Christen HJ, Hanefeld F.
    Brain Dev; 1986 Apr; 8(6):614-9. PubMed ID: 3103478
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  • 9. Merosin-positive congenital muscular dystrophy: a large inbred family.
    Mahjneh I, Bushby K, Anderson L, Muntoni F, Tolvanen-Mahjneh H, Bashir R, Pizzi A, Brockington M, Marconi G.
    Neuropediatrics; 1999 Feb; 30(1):22-8. PubMed ID: 10222457
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  • 11. Preserved merosin M-chain (or laminin-alpha 2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophy.
    Voit T, Sewry CA, Meyer K, Hermann R, Straub V, Muntoni F, Kahn T, Unsöld R, Helliwell TR, Appleton R.
    Neuropediatrics; 1995 Jun; 26(3):148-55. PubMed ID: 7477753
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  • 16. Merosin positive congenital muscular dystrophy with severe involvement of the central nervous system.
    De Stefano N, Dotti MT, Villanova M, Scarano G, Federico A.
    Brain Dev; 1996 Jun; 18(4):323-6. PubMed ID: 8879654
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  • 20. Congenital muscular dystrophy. Part I: a review of phenotypical and diagnostic aspects.
    Reed UC.
    Arq Neuropsiquiatr; 2009 Mar; 67(1):144-68. PubMed ID: 19330236
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