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Journal Abstract Search

146 related items for PubMed ID: 8888050

  • 1. Neonatal perifascicular myopathy.
    Nevo Y, Pestronk A.
    Pediatr Neurol; 1996 Sep; 15(2):150-2. PubMed ID: 8888050
    [Abstract] [Full Text] [Related]

  • 2. Pathologic quiz case: Male infant with generalized hypotonia and absence of respirations at birth,
    Kelly NA, Thomas C.
    Arch Pathol Lab Med; 2001 Apr; 125(4):575-6. PubMed ID: 11260644
    [No Abstract] [Full Text] [Related]

  • 3. RIG-I expression in perifascicular myofibers is a reliable biomarker of dermatomyositis.
    Suárez-Calvet X, Gallardo E, Pinal-Fernandez I, De Luna N, Lleixà C, Díaz-Manera J, Rojas-García R, Castellví I, Martínez MA, Grau JM, Selva-O'Callaghan A, Illa I.
    Arthritis Res Ther; 2017 Jul 24; 19(1):174. PubMed ID: 28738907
    [Abstract] [Full Text] [Related]

  • 4. A fatal congenital myopathy with severe type I fibre atrophy, central nuclei and multicores.
    Lee YS, Yip WC.
    J Neurol Sci; 1981 May 24; 50(2):277-90. PubMed ID: 7229670
    [Abstract] [Full Text] [Related]

  • 5. [Cap myopathy: a case report].
    Muñoz-Jareño N, López-Martínez A, Martín Fernández-Mayoralas D, Meizoso-Latova T, Cabello A.
    Rev Neurol; 1981 May 24; 45(11):669-71. PubMed ID: 18050099
    [Abstract] [Full Text] [Related]

  • 6. [Congenital fiber disproportion: atrophy of type I fibers. Report of 11 cases].
    Levy JA, Alegro MS, Lusvarghi ES, Salum PN, Tsanaclis AM, Levy A.
    Arq Neuropsiquiatr; 1987 Jun 24; 45(2):153-8. PubMed ID: 3426422
    [Abstract] [Full Text] [Related]

  • 7. [Neonatal hypotonia of muscular origin: analysis of 50 cases].
    Floriach-Robert M, Cabello A, Simón De Las Heras R, Mateos Beato F.
    Neurologia; 2001 Jun 24; 16(6):245-53. PubMed ID: 11423041
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  • 9. The myopathology of floppy and hypotonic infants in Singapore.
    Premasiri MK, Lee YS.
    Pathology; 2003 Oct 24; 35(5):409-13. PubMed ID: 14555385
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  • 12. [Animal experiment and biopsy studies on the cause, manifestations and diagnostic relevance of perifascicular muscle fiber atrophy].
    Herrmann V.
    Z Gesamte Inn Med; 1985 Jul 15; 40(14):417-23. PubMed ID: 2931906
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  • 14. Congenital neuromuscular disease with type I fibre hypotrophy, ophthalmoplegia and myofibril degeneration.
    Sugie H, Hanson R, Rasmussen G, Verity MA.
    J Neurol Neurosurg Psychiatry; 1982 Jun 15; 45(6):507-12. PubMed ID: 7119813
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  • 17. [Muscle biopsy in children: Usefulness in 2012].
    Cuisset JM, Maurage CA, Carpentier A, Briand G, Thévenon A, Rouaix N, Vallée L.
    Rev Neurol (Paris); 2013 Jun 15; 169(8-9):632-9. PubMed ID: 23993361
    [Abstract] [Full Text] [Related]

  • 18. [Nemaline myopathy as a cause of neonatal hypotonia - with emphasis on personal experiences. Report of a family with two brothers affected].
    Bojdo A, Obersztyn E, Wallgren-Pettersson C, Lehtokari V, Laing N, Davis M, Kułakowska Z.
    Med Wieku Rozwoj; 2009 Jun 15; 13(1):5-10. PubMed ID: 19648653
    [Abstract] [Full Text] [Related]

  • 19. Type 1 fiber size disproportion: morphometric data from 37 children with myopathic, neuropathic, or idiopathic hypotonia.
    Iannaccone ST, Bove KE, Vogler CA, Buchino JJ.
    Pediatr Pathol; 1987 Jun 15; 7(4):395-419. PubMed ID: 2451237
    [Abstract] [Full Text] [Related]

  • 20. Muscle biopsy in hypotonic children.
    Jirásek A, Kocura P.
    Acta Univ Carol Med Monogr; 1976 Jun 15; (75):35-6. PubMed ID: 1052638
    [No Abstract] [Full Text] [Related]

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