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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]
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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]
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