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Journal Abstract Search

493 related items for PubMed ID: 11001821

  • 1.
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  • 2. Surplus protein myopathies.
    Goebel HH, Warlo IA.
    Neuromuscul Disord; 2001 Jan; 11(1):3-6. PubMed ID: 11166159
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  • 6. Electron microscopy in neuromuscular disorders.
    Fernandez C, Figarella-Branger D, Meyronet D, Cassote E, Tong S, Pellissier JF.
    Ultrastruct Pathol; 2005 Jan; 29(6):437-50. PubMed ID: 16316944
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  • 8. Progress in desmin-related myopathies.
    Goebel HH, Warlo IA.
    J Child Neurol; 2000 Sep; 15(9):565-72. PubMed ID: 11019786
    [Abstract] [Full Text] [Related]

  • 9. Desminopathies in muscle disease.
    Paulin D, Huet A, Khanamyrian L, Xue Z.
    J Pathol; 2004 Nov; 204(4):418-27. PubMed ID: 15495235
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  • 10. A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathy.
    Vicart P, Caron A, Guicheney P, Li Z, Prévost MC, Faure A, Chateau D, Chapon F, Tomé F, Dupret JM, Paulin D, Fardeau M.
    Nat Genet; 1998 Sep; 20(1):92-5. PubMed ID: 9731540
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  • 11. Congenital myopathies at their molecular dawning.
    Goebel HH.
    Muscle Nerve; 2003 May; 27(5):527-48. PubMed ID: 12707973
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  • 13. Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients.
    Selcen D, Ohno K, Engel AG.
    Brain; 2004 Feb; 127(Pt 2):439-51. PubMed ID: 14711882
    [Abstract] [Full Text] [Related]

  • 14. Actin myopathy with nemaline bodies, intranuclear rods, and a heterozygous mutation in ACTA1 (Asp154Asn).
    Schröder JM, Durling H, Laing N.
    Acta Neuropathol; 2004 Sep; 108(3):250-6. PubMed ID: 15221331
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  • 16. 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; 30(3):E490-9. PubMed ID: 19105189
    [Abstract] [Full Text] [Related]

  • 17. Different early pathogenesis in myotilinopathy compared to primary desminopathy.
    Fischer D, Clemen CS, Olivé M, Ferrer I, Goudeau B, Roth U, Badorf P, Wattjes MP, Lutterbey G, Kral T, van der Ven PF, Fürst DO, Vicart P, Goldfarb LG, Moza M, Carpen O, Reichelt J, Schröder R.
    Neuromuscul Disord; 2006 Jun; 16(6):361-7. PubMed ID: 16684602
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  • 19. Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy.
    Nowak KJ, Wattanasirichaigoon D, Goebel HH, Wilce M, Pelin K, Donner K, Jacob RL, Hübner C, Oexle K, Anderson JR, Verity CM, North KN, Iannaccone ST, Müller CR, Nürnberg P, Muntoni F, Sewry C, Hughes I, Sutphen R, Lacson AG, Swoboda KJ, Vigneron J, Wallgren-Pettersson C, Beggs AH, Laing NG.
    Nat Genet; 1999 Oct; 23(2):208-12. PubMed ID: 10508519
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  • 20. [Myofibrillar myopathies].
    Olivé-Plana M.
    Rev Neurol; 1999 Oct; 37(8):770-2. PubMed ID: 14593638
    [Abstract] [Full Text] [Related]

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