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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 17, 2006
Readthrough strategies for stop codons in Duchenne muscular dystrophyS Aurino, V NigroEcotoxicology (London, England)|December 12, 2012
Metals loads into the Mediterranean Sea: estimate of Sarno River inputs and ecological riskP Montuori, P Lama, S Aurino, et al.Neurology|April 22, 2009
Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypesM Fanin, A C Nascimbeni, S Aurino, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 28, 2011
Mendelian bases of myopathies, cardiomyopathies, and neuromyopathiesG Piluso, S Aurino, M Cacciottolo, et al.Developmental Medicine and Child Neurology|March 18, 2006
Early onset calpainopathy with normal non-functional calpain 3 levelR Lanzillo, S Aurino, M Fanin, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 29, 2009
Candidate-gene testing for orphan limb-girdle muscular dystrophiesS Aurino, G Piluso, V Saccone, et al.Clinical Genetics|August 5, 2010
Novel missense mutations and unexpected multiple changes of RYR1 gene in 75 malignant hyperthermia familiesA Tammaro, A Di Martino, A Bracco, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|June 9, 2005
Beta-sarcoglycan gene mutations in TurkeyB Balci, E Wilichowski, G Haliloğlu, et al.Journal of Medical Genetics|September 6, 2005
Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypesG Piluso, L Politano, S Aurino, et al.Pageof 1