Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Clarissa, Locci"'
Autor:
Lucia Corrado, Fabiola De Marchi, Sara Tunesi, Gaia Donata Oggioni, Miryam Carecchio, Luca Magistrelli, Silvana Tesei, Giulio Riboldazzi, Alessio Di Fonzo, Clarissa Locci, Ilaria Trezzi, Roberta Zangaglia, Cristina Cereda, Sandra D’Alfonso, Corrado Magnani, Giacomo P. Comi, Giorgio Bono, Claudio Pacchetti, Roberto Cantello, Stefano Goldwurm, Cristoforo Comi
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
BackgroundAlpha-synuclein is a constituent of Lewy bodies and mutations of its gene cause familial Parkinson’s disease (PD). A previous study showed that a variant of the alpha-synuclein gene (SNCA), namely the 263 bp allele of Rep1 was associated
Externí odkaz:
https://doaj.org/article/774f3424aaa043409a9ea78888eb221a
Autor:
Diego Cotella, Nicola Ticozzi, Antonia Ratti, Claudia Colombrita, Letizia Mazzini, Fabiola De Marchi, Clarissa Locci, Sandra D'Alfonso, Alessandra Bagarotti, Hamid Hamzeiy, Vincenzo Silani, Lucia Corrado, Cinzia Tiloca, Ayşe Nazlı Başak, Nadia Barizzone
Large expansions of a noncoding GGGGCC repeat in the C9orf72 gene are the main cause of amyotrophic lateral sclerosis (ALS). The GGGGCC repeat is contiguous with another GC-rich region. Recent studies reported a significantly higher frequency of inse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::915b4e115c907c2fe118e4f1bd5fd4a8
Autor:
Lucia, Corrado, Fabiola, De Marchi, Sara, Tunesi, Gaia Donata, Oggioni, Miryam, Carecchio, Luca, Magistrelli, Silvana, Tesei, Giulio, Riboldazzi, Alessio, Di Fonzo, Clarissa, Locci, Ilaria, Trezzi, Roberta, Zangaglia, Cristina, Cereda, Sandra, D'Alfonso, Corrado, Magnani, Giacomo P, Comi, Giorgio, Bono, Claudio, Pacchetti, Roberto, Cantello, Stefano, Goldwurm, Cristoforo, Comi
Publikováno v:
Frontiers in Neurology
Background Alpha-synuclein is a constituent of Lewy bodies and mutations of its gene cause familial Parkinson’s disease (PD). A previous study showed that a variant of the alpha-synuclein gene (SNCA), namely the 263 bp allele of Rep1 was associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7e4f20133e46bea11584b7c209bc3d32
https://pubmed.ncbi.nlm.nih.gov/29662465
https://pubmed.ncbi.nlm.nih.gov/29662465
Autor:
Comi Giacomo Pietro, Sara Tunesi, Claudio Pacchetti, Silvana Tesei, Corrado Magnani, Cristoforo Comi, Clarissa Locci, Ilaria Trezzi, G.D. Oggioni, Sandra D'Alfonso, Roberta Zangaglia, Roberto Cantello, Stefano Goldwurm, Lucia Corrado, Miryam Carecchio, Giulio Riboldazzi, Fabiola De Marchi, Alessio Di Fonzo, Cristina Cereda, Luca Magistrelli, Giorgio Bono
α-synuclein is a constituent of Lewy bodies and mutations of its gene cause familial PD. A previous study showed that a variant of α-synuclein gene (SNCA), namely the 263bp allele of Rep1 was associated to faster motor progression in PD. On the con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf751c3280a15e912957266a70ff3d6c