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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

772 related items for PubMed ID: 18351526

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  • 6. Congenital muscular dystrophy in a new age.
    Day JW.
    Neurology; 2008 Jul 29; 71(5):308-9. PubMed ID: 18663176
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  • 7. Altered expression of ARPP protein in skeletal muscles of patients with muscular dystrophy, congenital myopathy and spinal muscular atrophy.
    Nakada C, Tsukamoto Y, Oka A, Nonaka I, Sato K, Mori S, Ito H, Moriyama M.
    Pathobiology; 2004 Jul 29; 71(1):43-51. PubMed ID: 14555844
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  • 8. Centronuclear myopathies: a widening concept.
    Romero NB.
    Neuromuscul Disord; 2010 Apr 29; 20(4):223-8. PubMed ID: 20181480
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  • 11. Muscular dystrophies and neurologic diseases that present as myopathy.
    Quan D.
    Rheum Dis Clin North Am; 2011 May 29; 37(2):233-44, vi. PubMed ID: 21444022
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  • 13. Muscle MRI in inherited neuromuscular disorders: past, present, and future.
    Mercuri E, Pichiecchio A, Allsop J, Messina S, Pane M, Muntoni F.
    J Magn Reson Imaging; 2007 Feb 29; 25(2):433-40. PubMed ID: 17260395
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  • 14. Gene expression analyses in X-linked myotubular myopathy.
    Noguchi S, Fujita M, Murayama K, Kurokawa R, Nishino I.
    Neurology; 2005 Sep 13; 65(5):732-7. PubMed ID: 16157907
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  • 15. Magnetic resonance imaging of muscle in congenital myopathies associated with RYR1 mutations.
    Jungbluth H, Davis MR, Müller C, Counsell S, Allsop J, Chattopadhyay A, Messina S, Mercuri E, Laing NG, Sewry CA, Bydder G, Muntoni F.
    Neuromuscul Disord; 2004 Dec 13; 14(12):785-90. PubMed ID: 15564033
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  • 19. A new phenotype of dysferlinopathy with congenital onset.
    Paradas C, González-Quereda L, De Luna N, Gallardo E, García-Consuegra I, Gómez H, Cabello A, Illa I, Gallano P.
    Neuromuscul Disord; 2009 Jan 13; 19(1):21-5. PubMed ID: 19084402
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