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Page 1
Infantile autosomal dominant distal myopathy.
Scoppetta C, Casali C, La Cesa I, Sermoni A, Mercuri B, Pierelli F, Vaccario ML. Scoppetta C, et al. Among authors: mercuri b. Acta Neurol Scand. 1995 Aug;92(2):122-6. doi: 10.1111/j.1600-0404.1995.tb01024.x. Acta Neurol Scand. 1995. PMID: 7484058 Review.
Cortical modulation of spinal excitability: an F-wave study.
Mercuri B, Wassermann EM, Manganotti P, Ikoma K, Samii A, Hallett M. Mercuri B, et al. Electroencephalogr Clin Neurophysiol. 1996 Feb;101(1):16-24. doi: 10.1016/0013-4694(95)00164-6. Electroencephalogr Clin Neurophysiol. 1996. PMID: 8625873
Autosomal recessive distal muscular dystrophy.
Scoppetta C, Mercuri B, Di Lello R, Tolli VS, Mennuni GF, Vaccario ML. Scoppetta C, et al. Among authors: mercuri b. Ital J Neurol Sci. 1997 Oct;18(5):271-6. doi: 10.1007/BF02083303. Ital J Neurol Sci. 1997. PMID: 9412850
Phenotypic variability in Bartter syndrome type I.
Bettinelli A, Ciarmatori S, Cesareo L, Tedeschi S, Ruffa G, Appiani AC, Rosini A, Grumieri G, Mercuri B, Sacco M, Leozappa G, Binda S, Cecconi M, Navone C, Curcio C, Syren ML, Casari G. Bettinelli A, et al. Among authors: mercuri b. Pediatr Nephrol. 2000 Sep;14(10-11):940-5. doi: 10.1007/pl00013418. Pediatr Nephrol. 2000. PMID: 10975303
25 results