Valdivia S, Ugaya CML, Hildenbrand J, Traverso M, Mazijn B, Sonnemann G. Dramatic effect of levetiracetam in early-onset epileptic encephalopathy due to STXBP1 mutation. PMID 26718981 DOI: 10.1016/J.Pediatrneurol.2015.11.004ĭilena R, Striano P, Traverso M, Viri M, Cristofori G, Tadini L, Barbieri S, Romeo A, Zara F. Genetic and Early Clinical Manifestations of Females Heterozygous for Duchenne/Becker Muscular Dystrophy. Papa R, Madia F, Bartolomeo D, Trucco F, Pedemonte M, Traverso M, Broda P, Bruno C, Zara F, Minetti C, Fiorillo C. Development of a Smartphone Application to Capture Carbohydrate, Lipid, and Protein Contents of Daily Food: Need for Integration in Artificial Pancreas for Patients With Type 1 Diabetes? Journal of Diabetes Science and Technology. PMID 3185434ĭiouri O, Place J, Traverso M, Georgescu V, Picot MC, Renard E. Lack of SLC2A1 (glucose transporter 1) mutations in 30 Italian patients with alternating hemiplegia of childhood. PMID 18487559 DOI: 10.1136/Jnnp.2007.133207ĭe Grandis E, Stagnaro M, Biancheri R, Giannotta M, Gobbi G, Traverso M, Veneselli E, Zara F. Journal of Neurology, Neurosurgery, and Psychiatry. Truncation of Caveolin-3 causes autosomal-recessive Rippling Muscle Disease. Traverso M, Bruno C, Broccolini A, Sotgia F, Donati MA, Assereto S, Gazzerro E, Lo Monaco M, Modoni A, D'Amico A, Gasperini S, Ricci E, Zara F, Lisanti M, Minetti C. PMID 27295345 DOI: 10.1038/labinvest.2016.63Ĭataldo F, La Monaca P, Schiavo G, Traverso MG, Iacono A, Albeggiani A. Laboratory Investigation a Journal of Technical Methods and Pathology. The ubiquitin ligase tripartite-motif-protein 32 is induced in Duchenne muscular dystrophy. PMID 15452297 DOI: 10.1212/01.Wnl.0000138429.11433.0DĪssereto S, Piccirillo R, Baratto S, Scudieri P, Fiorillo C, Massacesi M, Traverso M, Galietta LJ, Bruno C, Minetti C, Zara F, Gazzerro E.

Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV). PMID 14506725 DOI: 10.1002/mus.10429īruno C, van Diggelen OP, Cassandrini D, Gimpelev M, Giuffrè B, Donati MA, Introvini P, Alegria A, Assereto S, Morandi L, Mora M, Tonoli E, Mascelli S, Traverso M, Pasquini E, et al. Progressive exercise intolerance associated with a new muscle-restricted nonsense mutation (G142X) in the mitochondrial cytochrome b gene. PMID 18253147 DOI: 10.1038/Labinvest.3700713īruno C, Santorelli FM, Assereto S, Tonoli E, Tessa A, Traverso M, Scapolan S, Bado M, Tedeschi S, Minetti C. Caveolin-3 T78M and T78K missense mutations lead to different phenotypes in vivo and in vitro. Traverso M, Gazzerro E, Assereto S, Sotgia F, Biancheri R, Stringara S, Giberti L, Pedemonte M, Wang X, Scapolan S, Pasquini E, Donati MA, Zara F, Lisanti MP, Bruno C, et al. Identification of a hemerythrin-like domain in a P1B-type transport ATPase. Traverso ME, Subramanian P, Davydov R, Hoffman BM, Stemmler TL, Rosenzweig AC. Low-probability matches (unlikely to be authored by this person)

Matthew traverso