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Page 1
New therapies in muscular dystrophies.
Angelini C, Bonifati DM. Angelini C, et al. Neurol Sci. 2000;21(5 Suppl):S919-24. doi: 10.1007/s100720070004. Neurol Sci. 2000. PMID: 11382190 Review.
Decreased fatty acid beta-oxidation in riboflavin-responsive, multiple acylcoenzyme A dehydrogenase-deficient patients is associated with an increase in uncoupling protein-3.
Russell AP, Schrauwen P, Somm E, Gastaldi G, Hesselink MK, Schaart G, Kornips E, Lo SK, Bufano D, Giacobino JP, Muzzin P, Ceccon M, Angelini C, Vergani L. Russell AP, et al. J Clin Endocrinol Metab. 2003 Dec;88(12):5921-6. doi: 10.1210/jc.2003-030885. J Clin Endocrinol Metab. 2003. PMID: 14671191
Heart involvement in muscular dystrophies due to sarcoglycan gene mutations.
Melacini P, Fanin M, Duggan DJ, Freda MP, Berardinelli A, Danieli GA, Barchitta A, Hoffman EP, Dalla Volta S, Angelini C. Melacini P, et al. Muscle Nerve. 1999 Apr;22(4):473-9. doi: 10.1002/(sici)1097-4598(199904)22:4<473::aid-mus8>3.0.co;2-5. Muscle Nerve. 1999. PMID: 10204782
Coordinated and reversible reduction of enzymes involved in terminal oxidative metabolism in skeletal muscle mitochondria from a riboflavin-responsive, multiple acyl-CoA dehydrogenase deficiency patient.
Gianazza E, Vergani L, Wait R, Brizio C, Brambilla D, Begum S, Giancaspero TA, Conserva F, Eberini I, Bufano D, Angelini C, Pegoraro E, Tramontano A, Barile M. Gianazza E, et al. Electrophoresis. 2006 Mar;27(5-6):1182-98. doi: 10.1002/elps.200500687. Electrophoresis. 2006. PMID: 16470778
19 results