LabCAST


SessionReferences
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  2. Brooke, M. Disorders of Skeletal Muscle in Neurology in Clinical Practice, edited by W.E. Bradley, et al, 2187-2200. Boston: Butterworth-Heinemann, 2000.
  3. Kissel, JT. Fascioscapulohumeral Dystrophy. Seminars in Neurology 1999; 19(1): 35-43.
  4. Orrell, RW, et al. Definitive molecular diagnosis of fascioscapulohumeral dystrophy. Neurology 1999; 52: 1822-1826.
  5. Gnecchi-Ruscone, T, et al. Cardiomyopathy in duchenne, becker, and sarcoglycanopathies: a role for coronary dysfunction? Muscle & Nerve 1999; 22(11): 1549-1556.
  6. Tawil, R, et al. Fascioscapulohumeral Dystrophy: A Distinct Regional Myopathy with a Novel Molecular Pathogenesis. Annals of Neurology 1998; 43(3): 279-282.
  7. Brouwer, OF, et al. Early onset Fascioscapulohumeral muscular dystrophy. Muscle & Nerve 1995; Supp2: S67-S72.
  8. Darras, B. Molecular genetics of Duchenne and Becker muscular dystrophy. The Journal of Pediatrics 1990; 117(1): 1-15.
  9. Blumen, SC, et al. Homozygotes for Oculopharyngeal Muscular Dystrophy Have a Severe Form of the Disease. Annals of Neurology 1999; 46: 115-118.
  10. Thompson, MW. The Genetic Transmission of Muscle Diseases in Myology: Basic and Clinical, 2nd ed. Edited by A.G. Engel, et al, 1078. New York: McGraw-Hill Inc., 1994.