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Journal Abstract Search

135 related items for PubMed ID: 8922062

  • 1. Familial desmin myopathies and cytoplasmic body myopathies.
    Baeta AM, Figarella-Branger D, Bille-Turc F, Lepidi H, Pellissier JF.
    Acta Neuropathol; 1996 Nov; 92(5):499-510. PubMed ID: 8922062
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  • 2. [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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  • 3. Familial cardiomyopathy and distal myopathy with abnormal desmin accumulation and migration.
    Lobrinus JA, Janzer RC, Kuntzer T, Matthieu JM, Pfend G, Goy JJ, Bogousslavsky J.
    Neuromuscul Disord; 1998 Apr; 8(2):77-86. PubMed ID: 9608560
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  • 4. Progress in desmin-related myopathies.
    Goebel HH, Warlo IA.
    J Child Neurol; 2000 Sep; 15(9):565-72. PubMed ID: 11019786
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  • 5. Expression of the intermediate filament protein synemin in myofibrillar myopathies and other muscle diseases.
    Olivé M, Goldfarb L, Dagvadorj A, Sambuughin N, Paulin D, Li Z, Goudeau B, Vicart P, Ferrer I.
    Acta Neuropathol; 2003 Jul; 106(1):1-7. PubMed ID: 12669240
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  • 6. Desmin-related myopathies.
    Goebel HH.
    Curr Opin Neurol; 1997 Oct; 10(5):426-9. PubMed ID: 9330890
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  • 7. Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene.
    Dalakas MC, Park KY, Semino-Mora C, Lee HS, Sivakumar K, Goldfarb LG.
    N Engl J Med; 2000 Mar 16; 342(11):770-80. PubMed ID: 10717012
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  • 9. Myofibrillar (desmin-related) myopathy: clinico-pathological spectrum in 3 cases and review of the literature.
    Wanschit J, Nakano S, Goudeau B, Ströbel T, Rinner W, Wimmer G, Resch H, Jaksch M, Akiguchi I, Vicart P, Budka H.
    Clin Neuropathol; 2002 Mar 16; 21(5):220-31. PubMed ID: 12365725
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  • 10. Spheroid-cytoplasmic complexes in a congenital myopathy.
    Halbig L, Goebel HH, Hopf HC, Moll R.
    Rev Neurol (Paris); 1991 Mar 16; 147(4):300-7. PubMed ID: 1648255
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  • 11. Desmin-related myopathy: clinical, electrophysiological, radiological, neuropathological and genetic studies.
    Olivé M, Goldfarb L, Moreno D, Laforet E, Dagvadorj A, Sambuughin N, Martínez-Matos JA, Martínez F, Alió J, Farrero E, Vicart P, Ferrer I.
    J Neurol Sci; 2004 Apr 15; 219(1-2):125-37. PubMed ID: 15050448
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  • 15. Spheroid body myopathy revisited.
    Goebel HH, D'Agostino AN, Wilson J, Cole G, Foroud T, Koller D, Farlow M, Azzarelli B, Muller J.
    Muscle Nerve; 1997 Sep 15; 20(9):1127-36. PubMed ID: 9270668
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  • 16. Desmin-related neuromuscular disorders.
    Goebel HH.
    Muscle Nerve; 1995 Nov 15; 18(11):1306-20. PubMed ID: 7565929
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  • 18. A novel desmin R355P mutation causes cardiac and skeletal myopathy.
    Fidziańska A, Kotowicz J, Sadowska M, Goudeau B, Walczak E, Vicart P, Hausmanowa-Petrusewicz I.
    Neuromuscul Disord; 2005 Aug 15; 15(8):525-31. PubMed ID: 16009553
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  • 19. How much mutant protein is needed to cause a protein aggregate myopathy in vivo? Lessons from an exceptional desminopathy.
    Clemen CS, Fischer D, Reimann J, Eichinger L, Müller CR, Müller HD, Goebel HH, Schröder R.
    Hum Mutat; 2009 Mar 15; 30(3):E490-9. PubMed ID: 19105189
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  • 20. Familial desminopathy: myopathy with accumulation of desmin-type intermediate filaments.
    Vajsar J, Becker LE, Freedom RM, Murphy EG.
    J Neurol Neurosurg Psychiatry; 1993 Jun 15; 56(6):644-8. PubMed ID: 8509778
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