Emery-Dreiffus Muscular Dystrophy: MR Imaging and Spectroscopy in the Brain and Skeletal Muscle

References

1. ↵
   Mercuri E, Counsell S, Allsop J, et al. Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy. Neuropediatrics 2002;33:10–14

   CrossRefPubMed
2. Sewry CA, Brown SC, Mercuri E, et al. Skeletal muscle pathology in autosomal dominant Emery-Dreifuss muscular dystrophy with lamin A/C mutations. Neuropathol Appl Neurobiol 2001;27:281–290

   CrossRefPubMedWeb of Science
3. Rowland LP, Fetell M, Olarte M, et al. Emery-Dreifuss muscular dystrophy. Ann Neurol 1979;5:111–117

   CrossRefPubMedWeb of Science
4. Miller RG, Layzer RB, Mellenthin MA, et al. Emery-Dreifuss muscular dystrophy with autosomal dominant transmission. Neurology 1985;35:1230–1233

   Abstract/FREE Full Text
5. Galassi G, Modena MG, Benassi A, et al. Autosomal-dominant dystrophy with humeroperoneal weakness and cardiopathy: a genetic variant of Emery-Dreifuss disease? Ital J Neurol Sci 1986;7:125–132

   CrossRefPubMed
6. Emery AE. Emery-Dreifuss muscular dystrophy: a 40-year retrospective. Neuromuscul Disord 2000;10:228–232

   CrossRefPubMedWeb of Science
7. Zacharias AS, Wagener ME, Warren ST, Hopkins LC. Emery-Dreifuss muscular dystrophy. Semin Neurol 1999;19:67–79

   PubMed
8. ↵
   Helbling-Leclerc A, Bonne G, Schwartz K. Emery-Dreifuss muscular dystrophy. Eur J Hum Genet 2002;10:157–161

   CrossRefPubMed
9. ↵
   Barkovich AJ. Neuroimaging manifestations and classification of congenital muscular dystrophies. AJNR Am J Neuroradiol 1998;19:1389–1396

   Abstract
10. ↵
    van der Knaap MS, Smit LM, Barth PG, et al. Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities. Ann Neurol 1997;42:50–59

    CrossRefPubMedWeb of Science
11. ↵
    Yoshida T. The rate of phosphocreatine hydrolysis and resynthesis in exercising muscle in humans using 31P-MRS. J Physiol Anthropol Appl Human Sci 2002;21:247–255

    CrossRefPubMed