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Ophthalmoplegia, demyelinating neuropathy, leukoencephalopathy, myopathy, and gastrointestinal dysfunction with multiple deletions of mitochondrial DNA: a mitochondrial multisystem disorder in search of a name.
Uncini A, Servidei S, Silvestri G, Manfredi G, Sabatelli M, Di Muzio A, Ricci E, Mirabella M, Di Mauro S, Tonali P. Uncini A, et al. Among authors: silvestri g. Muscle Nerve. 1994 Jun;17(6):667-74. doi: 10.1002/mus.880170616. Muscle Nerve. 1994. PMID: 8196710
Functional involvement of central nervous system in mitochondrial disorders.
Di Lazzaro V, Restuccia D, Servidei S, Valeriani M, Nardone R, Manfredi G, Silvestri G, Ricci E, Tonali P. Di Lazzaro V, et al. Among authors: silvestri g. Electroencephalogr Clin Neurophysiol. 1997 Jun;105(3):171-80. doi: 10.1016/s0924-980x(97)96671-6. Electroencephalogr Clin Neurophysiol. 1997. PMID: 9216485
Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype.
Ricci E, Galluzzi G, Deidda G, Cacurri S, Colantoni L, Merico B, Piazzo N, Servidei S, Vigneti E, Pasceri V, Silvestri G, Mirabella M, Mangiola F, Tonali P, Felicetti L. Ricci E, et al. Among authors: silvestri g. Ann Neurol. 1999 Jun;45(6):751-7. doi: 10.1002/1531-8249(199906)45:6<751::aid-ana9>3.0.co;2-m. Ann Neurol. 1999. PMID: 10360767
1,087 results