RE-BVS – Piemonte Repository

Sfoglia per AUTORE
DUGA S
Collezione AOU Novara

Items : 5

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis. in JAMA neurology / JAMA Neurol. 2021 Oct 1;78(10):1236-1248. doi: 10.1001/jamaneurol.2021.2598.

2021
AOU Città della Salute di Torino
AOU Novara

Tremolizzo L; Trojsi F; Torriello A; Tranquilli S; Tedeschi G; Ticca A; Tanel R; Simonini C; Spataro R; Simone I; Sbaiz L; Sideri R; Santarelli M; Salivetto M; Salvi F; Sabatelli M; Salamone P; Riolo G; Riva N; Russo M; Ricci C; Pugliatti M; Quattrini A; Pozzi S; Petrelli C; Petrucci A; Passaniti C; Origone P; Murru MR; et alii...

X Chromosome Contribution to the Genetic Architecture of Primary Biliary Cholangitis. in Gastroenterology / Gastroenterology. 2021 Jun;160(7):2483-2495.e26. doi: 10.1053/j.gastro.2021.02.061. Epub 2021 Mar 4.

2021
AO Cuneo
AOU Novara

Cardamone G; Carbone M; Siminovitch KA; Hirschfield G; Xiong M; Liu X; Shi Y; Li Z; Tanaka A; Tang R; Nagasaki M; Tokunaga K; Kawashima M; Nishida N; Ueno K; Hitomi Y; Jones DE; Nakamura M; Mells GF; Sandford RN; Cordell HJ; Gerussi A; Asselta R; Paraboschi EM; Duga S; Gershwin ME; Seldin MF; Invernizzi P;

Survival and dementia in GBA-associated Parkinson's disease: The mutation matters. in Annals of neurology / Ann Neurol. 2016 Nov;80(5):662-673. doi: 10.1002/ana.24777. Epub 2016 Oct 3.

2016
AOU Città della Salute di Torino
AOU Novara

Seresini A; Soldà G; Asselta R; Duga S; Magnani C; Barichella M; Zini M; Sacilotto G; Meucci N; Mariani CB; Canesi M; Tesei S; Zecchinelli AL; Siri C; Cereda E; Marotta G; Tunesi S; Cilia R; Seia M; Pezzoli G; Goldwurm S;

Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS. in Neuron / Neuron. 2014 Oct 22;84(2):324-31. doi: 10.1016/j.neuron.2014.09.027. Epub 2014 Oct 22.

2014
AOU Novara

Smith BN; Ticozzi N; Fallini C; Gkazi AS; Topp S; Kenna KP; Scotter EL; Kost J; Keagle P; Miller JW; Calini D; Vance C; Danielson EW; Troakes C; Tiloca C; Al-Sarraj S; Lewis EA; King A; Colombrita C; Pensato V; Castellotti B; de Belleroche J; Baas F; ten Asbroek AL; Sapp PC; McKenna-Yasek D; McLaughlin RL; Polak M; Asress S; et alii...

Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. in Human molecular genetics / Hum Mol Genet. 2014 Dec 20;23(25):6746-61. doi: 10.1093/hmg/ddu392. Epub 2014 Jul 30.

2014
AOU Novara

Paraboschi EM; Rimoldi V; Soldà G; Tabaglio T; Dall'Osso C; Saba E; Vigliano M; Salviati A; Leone M; Benedetti MD; Fornasari D; Saarela J; De Jager PL; Patsopoulos NA; D'Alfonso S; Gemmati D; Duga S; Asselta R;