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Journal Abstract Search

287 related items for PubMed ID: 11571700

  • 1. Reducing body myopathy with cytoplasmic bodies and rigid spine syndrome: a mixed congenital myopathy.
    Goebel HH, Halbig LE, Goldfarb L, Schober R, Albani M, Neuen-Jacob E, Voit T.
    Neuropediatrics; 2001 Aug; 32(4):196-205. PubMed ID: 11571700
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  • 3. Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles.
    Darin N, Kyllerman M, Wahlström J, Martinsson T, Oldfors A.
    Ann Neurol; 1998 Aug; 44(2):242-8. PubMed ID: 9708547
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  • 4. [Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material without mutation of the alphabeta-crystallin gene].
    Pou Serradell A, Lloreta Trull J, Corominas Torres J, Guicheney P.
    Neurologia; 2001 May; 16(5):195-203. PubMed ID: 11412718
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  • 8. Inclusion body myopathy associated with motor neuron syndrome: three case reports.
    Cafforio G, Pistolesi S, D'Avino C, Galluzzi F, Patricelli A, Solito B, Fontanini G, Siciliano G.
    Clin Neuropathol; 2005 May; 24(1):36-41. PubMed ID: 15696783
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  • 9. Myopathy with tubulin-reactive inclusions in two cats.
    Shelton GD, Sturges BK, Lyons LA, Williams DC, Aleman M, Jiang Y, Mizisin AP.
    Acta Neuropathol; 2007 Nov; 114(5):537-42. PubMed ID: 17393175
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  • 10. Sarcoplasmic body myopathy--a rare hereditary myopathy with characteristic inclusions.
    Engvall M, Ahlberg G, Hedberg B, Edström L, Ansved T.
    Acta Neurol Scand; 2005 Oct; 112(4):223-7. PubMed ID: 16146490
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  • 14. [Unilateral presentation of X-linked myotubular myopathy (XLMTM) in two out of three female carriers in a family with no affected male].
    Drouet A, Ollagnon-Roman E, Streichenberger N, Biancalana V, Cossée M, Guilloton L, Petiot P.
    Rev Neurol (Paris); 2008 Feb; 164(2):169-76. PubMed ID: 18358876
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  • 17. [Congenital myopathies].
    Cabello A, Ricoy-Campo JR.
    Rev Neurol; 2008 Feb; 37(8):779-86. PubMed ID: 14593641
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  • 18. IBM-type inclusions in a patient with slow-channel syndrome caused by a mutation in the AChR epsilon subunit.
    Fidzianska A, Ryniewicz B, Shen XM, Engel AG.
    Neuromuscul Disord; 2005 Nov; 15(11):753-9. PubMed ID: 16198106
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  • 19. Consequences of mutations within the C terminus of the FHL1 gene.
    Schoser B, Goebel HH, Janisch I, Quasthoff S, Rother J, Bergmann M, Müller-Felber W, Windpassinger C.
    Neurology; 2009 Aug 18; 73(7):543-51. PubMed ID: 19687455
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  • 20. Rimmed vacuoles with beta-amyloid and tau protein deposits in the muscle of children with hereditary myopathy.
    Fidziańska A, Glinka Z.
    Acta Neuropathol; 2006 Aug 18; 112(2):185-93. PubMed ID: 16788822
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