Nicola Migone
Nicola Migone
affiliation: Università di Torino
research area(s): Genetics And Genomics
Course: Biomedical Sciences and Human Oncology
University/Istitution: Università di Torino
Petrelli A, Gilestro GF, Lanzardo S, Comoglio PM, Migone N, Giordano S. 2002. The endophilin-CIN85-Cbl complex mediates ligand-dependent down-regulation of c-Met. Nature 416:187-190.

Brusco A, Gellera C, Cagnoli C, Saluto A, Castucci A, Michielotto C, Fetoni V, Mariotti C, Migone N, Di Donato S, Taroni F. 2004. Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of SCA genes and CAG/CTG repeat expansion detection in 225 Italian families. Arch Neurol 61:727-733.

Brussino A, Gellera C, Saluto A, Mariotti C, Arduino C, Castellotti B, Camerlingo M, de Angelis V, Orsi L, Tosca P, Migone N, Taroni F, Brusco A. 2005. FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia. Neurology 64:145-147.

Cagnoli C, Mariotti C, Taroni F, Seri M, Brussino A, Michielotto C, Grisoli M, Di Bella D, Migone N, Gellera C, DiDonato S, Brusco A. 2006. SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2. Brain 129:235-242.

Guerra MP, Cavalleri F, Migone N, Lugli L, Delalande O, Cavazzuti GB, Ferrari F. 2007. Intractable epilepsy in hemimegalencephaly and tuberous sclerosis complex. J Child Neurol 22:80-84.

Cavalieri S, Funaro A, Pappi P, Migone N, Gatti RA, Brusco A. 2008. Large genomic mutations within the ATM gene detected by MLPA, including a duplication of 41 kb from exon 4 to 20. Ann Hum Genet 72:10-8.

Cagnoli C, Brussino A, Di Gregorio E, Caroppo P, Stola S, Dragone E, Ferrone M, Padovan S, Migone N, Orsi L, Brusco A. 2008. Mutations in the POLG1 gene are not a relevant cause of cerebellar ataxia in Italy. J Neurol 255:1079-80.

Cagnoli C, Brussino A, Sbaiz L, Di Gregorio E, Atzori C, Caroppo P, Orsi L, Migone N, Buffa C, Imperiale D, Brusco A. 2008. A previously undiagnosed case of Gerstmann-Sträussler-Scheinker disease revealed by PRNP gene analysis in patients with adult-onset ataxia. Mov Disord 23:1468-71.

Brussino A, Vaula G, Cagnoli C, Mauro A, Pradotto L, Daniele D, Di Gregorio E, Barberis M, Arduino C, Squadrone S, Abete MC, Migone N, Calabrese O, Brusco A. 2009. A novel family with Lamin B1 duplication associated with adult-onset leucoencephalopathy. J Neurol Neurosurg Psychiatry 80:237-40.

Brussino A, D'Alfonso S, Cagnoli C, Di Gregorio E, Barberis M, Padovan S, Vaula G, Pinessi L, Squadrone S, Abete MC, Collimedaglia L, Guerini FR, Migone N, Brusco A. 2009. Mutations in the lamin B1 gene are not present in multiple sclerosis. Eur J Neurol 16:544-6.

Cagnoli C, Stevanin G, Brussino A, Barberis M, Mancini C, Margolis RL, Holmes SE, Nobili M, Forlani S, Padovan S, Pappi P, Zaros C, Leber I, Ribai P, Pugliese L, Assalto C, Brice A, Migone N, Dürr A, Brusco A. 2010. Missense mutations in the AFG3L2 proteolytic domain account for 1.5% of European autosomal dominant cerebellar ataxias. Hum Mutat 31:1117-24.

Brussino A, Graziano C, Giobbe D, Ferrone M, Dragone E, Arduino C, Lodi R, Tonon C, Gabellini A, Rinaldi R, Miccoli S, Grosso E, Bellati MC, Orsi L, Migone N, Brusco A. 2010. Spinocerebellar ataxia type 12 identified in two Italian families may mimic sporadic ataxia. Mov Disord 25:1269-73.
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