These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 9270668)

  • 1. 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; 20(9):1127-36. PubMed ID: 9270668
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal dominant distal myopathy with desmin storage: a clinicopathologic and electrophysiologic study of a large kinship.
    Horowitz SH; Schmalbruch H
    Muscle Nerve; 1994 Feb; 17(2):151-60. PubMed ID: 8114783
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Spheroid-cytoplasmic complexes in a congenital myopathy.
    Halbig L; Goebel HH; Hopf HC; Moll R
    Rev Neurol (Paris); 1991; 147(4):300-7. PubMed ID: 1648255
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hereditary distal myopathy with granulo-filamentous cytoplasmic inclusions containing desmin, dystrophin and vimentin.
    Helliwell TR; Green AR; Green A; Edwards RH
    J Neurol Sci; 1994 Jul; 124(2):174-87. PubMed ID: 7964869
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Glucocorticoid treatment induces expression of small heat shock proteins in human satellite cell populations: consequences for a desmin-related myopathy involving the R120G alpha B-crystallin mutation.
    Nédellec P; Edling Y; Perret E; Fardeau M; Vicart P
    Neuromuscul Disord; 2002 Jun; 12(5):457-65. PubMed ID: 12031619
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial desminopathy: myopathy with accumulation of desmin-type intermediate filaments.
    Vajsar J; Becker LE; Freedom RM; Murphy EG
    J Neurol Neurosurg Psychiatry; 1993 Jun; 56(6):644-8. PubMed ID: 8509778
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two related Dutch families with a clinically variable presentation of cardioskeletal myopathy caused by a novel S13F mutation in the desmin gene.
    Bergman JE; Veenstra-Knol HE; van Essen AJ; van Ravenswaaij CM; den Dunnen WF; van den Wijngaard A; van Tintelen JP
    Eur J Med Genet; 2007; 50(5):355-66. PubMed ID: 17720647
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A mutation in myotilin causes spheroid body myopathy.
    Foroud T; Pankratz N; Batchman AP; Pauciulo MW; Vidal R; Miravalle L; Goebel HH; Cushman LJ; Azzarelli B; Horak H; Farlow M; Nichols WC
    Neurology; 2005 Dec; 65(12):1936-40. PubMed ID: 16380616
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Autosomal dominant late adult onset distal leg myopathy.
    Pénisson-Besnier I; Dumez C; Chateau D; Dubas F; Fardeau M
    Neuromuscul Disord; 1998 Oct; 8(7):459-66. PubMed ID: 9829275
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A new type of hereditary distal myopathy with characteristic sarcoplasmic bodies and intermediate (skeletin) filaments.
    Edström L; Thornell LE; Eriksson A
    J Neurol Sci; 1980 Aug; 47(2):171-90. PubMed ID: 6251174
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Storage of phosphorylated desmin in a familial myopathy.
    Rappaport L; Contard F; Samuel JL; Delcayre C; Marotte F; Tomè F; Fardeau M
    FEBS Lett; 1988 Apr; 231(2):421-5. PubMed ID: 3360147
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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(8):525-31. PubMed ID: 16009553
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autosomal dominant hyaline body myopathy: clinical variability and pathologic findings.
    Bohlega S; Lach B; Meyer BF; Al Said Y; Kambouris M; Al Homsi M; Cupler EJ
    Neurology; 2003 Dec; 61(11):1519-23. PubMed ID: 14663035
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Myopathy associated with desmin type intermediate filaments. An immunoelectron microscopic study.
    Pellissier JF; Pouget J; Charpin C; Figarella D
    J Neurol Sci; 1989 Jan; 89(1):49-61. PubMed ID: 2926442
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Reducing body myopathy and desmin storage in skeletal muscle: morphological and biochemical findings.
    Bertini E; Salviati G; Apollo F; Ricci E; Servidei S; Broccolini A; Papacci M; Tonali P
    Acta Neuropathol; 1994; 87(1):106-12. PubMed ID: 8140891
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Centronuclear myopathy with autosomal dominant inheritance.
    McLeod JG; Baker Wde C; Lethlean AK; Shorey CD
    J Neurol Sci; 1972 Apr; 15(4):375-87. PubMed ID: 5016690
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.