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Journal Abstract Search

99 related items for PubMed ID: 8122880

  • 1. Rapidly evolving myopathy with myosin-deficient muscle fibers.
    al-Lozi MT, Pestronk A, Yee WC, Flaris N, Cooper J.
    Ann Neurol; 1994 Mar; 35(3):273-9. PubMed ID: 8122880
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  • 5. Clinical and histologic changes in the follow-up of a congenital myopathy.
    Camacho A, Villarejo A, Simón R, Mateos F, Cabello A.
    Pediatr Neurol; 2005 Aug; 33(2):139-41. PubMed ID: 16087062
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  • 8. Fiber density in congenital muscle fiber type disproportion. II. Congenital muscle hypotonia and hip dislocation.
    Rowińska-Marcińska K, Strugalska MH, Hausmanowa-Petrusewicz I.
    Electromyogr Clin Neurophysiol; 1991 Aug; 31(1):5-8. PubMed ID: 2009826
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  • 9. Congenital myopathy with type 2A muscle fiber uniformity and smallness.
    Gallanti A, Prelle A, Chianese L, Barbieri S, Jann S, Schiaffino S, Comini A, Scarpini E, Pellegrini G, Moggio M.
    Neuropediatrics; 1992 Feb; 23(1):10-3. PubMed ID: 1565211
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  • 11. Fetal muscle characteristics in nemaline myopathy.
    Nonaka I, Tojo M, Sugita H.
    Neuropediatrics; 1983 Feb; 14(1):47-52. PubMed ID: 6682187
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  • 12. Diagnosis of mitochondrial diseases: clinical and histological study of sixty patients with ragged red fibers.
    Challa S, Kanikannan MA, Murthy JM, Bhoompally VR, Surath M.
    Neurol India; 2004 Sep; 52(3):353-8. PubMed ID: 15472426
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  • 15. Necrotising myopathy, an unusual presentation of a steroid-responsive myopathy.
    Bronner IM, Hoogendijk JE, Wintzen AR, van der Meulen MF, Linssen WH, Wokke JH, de Visser M.
    J Neurol; 2003 Apr; 250(4):480-5. PubMed ID: 12700915
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  • 16. Myosin storage myopathy: slow skeletal myosin (MYH7) mutation in two isolated cases.
    Laing NG, Ceuterick-de Groote C, Dye DE, Liyanage K, Duff RM, Dubois B, Robberecht W, Sciot R, Martin JJ, Goebel HH.
    Neurology; 2005 Feb 08; 64(3):527-9. PubMed ID: 15699387
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