Sfoglia per AUTORE
BRICE A
Collezione AOU Città della Salute di Torino

  

Items : 9

2022
AOU Città della Salute di Torino
AOU Novara
ASL Torino 4
ASL Asti
ASL Biella
ASL Vercelli

Silani V; Weber M; Rouleau GA; Pinto S; de Carvalho M; Petri S; Wallace L; Henders AK; Curtis CJ; Breen G; Sachdev PS; Mather KA; Williams KL; Steyn FJ; Rowe DB; Pamphlett R; Nicholson GA; Ngo ST; Needham M; McCombe PA; Mathers S; Furlong S; Henderson RD; Benyamin B; Kiernan MC; Blair IP; Povedano M; Stevi? Z; Drory V; et alii...

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...

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture. in Nature genetics / Nat Genet. 2021 Mar;53(3):294-303. doi: 10.1038/s41588-021-00785-3. Epub 2021 Feb 15.
2021
AOU Città della Salute di Torino

Morenas-Rodriguez E; Kukull WA; Faber K; Pickering-Brown S; Albani D; Ferrari R; Morris HR; Scherzer CR; Bennett DA; Goate A; Renton AE; Kuzma A; Leverenz JB; Besser LM; Bekris LM; Pastor P; Woltjer R; Kaiser SM; Klein G; Aarsland D; Hodges AK; Al-Sarraj S; Troakes C; Love S; Palmer L; Morris CM; Attems J; Thomas AJ; McKeith IG; et alii...

2021
AOU Città della Salute di Torino
AOU Novara
ASL Torino 4
ASL Asti
ASL Biella
ASL Vercelli

Sachdev PS; Mather KA; Williams KL; Steyn FJ; Rowe DB; Pamphlett R; Nicholson GA; Ngo ST; Needham M; McCombe PA; Mathers S; Furlong S; Henderson RD; Benyamin B; Kiernan MC; Blair IP; Povedano M; Stevi? Z; Drory V; Glava? D; Ravnik-Glava? M; Zidar J; Koritnik B; Rogelj B; Ataulina A; Demeshonok V; Fominykh V; Brylev L; Hübner CA; et alii...

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. in Nature genetics / Nat Genet. 2016 Sep;48(9):1043-8. doi: 10.1038/ng.3622. Epub 2016 Jul 25.
2016
AOU Città della Salute di Torino
AOU Novara

Casale F; Leigh PN; Hübner CA; Kurth I; Stubendorff B; Prell T; Ringer T; Witte OW; Grosskreutz J; Kiernan MC; Pamphlett R; Rowe DB; Nicholson GA; Fifita JA; McCann EP; Zhang K; Stuit RJ; Blair I; Muller B; Filosto M; Padovani A; Riva N; Penco S; Lunetta C; Zecca C; Capozzo R; Brunetti M; Arcuti S; Moglia C; et alii...

A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia. in American journal of human genetics / Am J Hum Genet. 2015 Nov 5;97(5):726-37. doi: 10.1016/j.ajhg.2015.09.007. Epub 2015 Oct 8.
2015
AOU Città della Salute di Torino

Coutelier M; Blesneac I; Monteil A; Monin ML; Ando K; Mundwiller E; Brusco A; Le Ber I; Anheim M; Castrioto A; Duyckaerts C; Brice A; Durr A; Lory P; Stevanin G;

Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes. in Brain : a journal of neurology / Brain. 2014 Sep;137(Pt 9):2444-55. doi: 10.1093/brain/awu174. Epub 2014 Jun 26.
2014
AOU Città della Salute di Torino

Tezenas du Montcel S; Durr A; Bauer P; Figueroa KP; Ichikawa Y; Brussino A; Forlani S; Rakowicz M; Schöls L; Mariotti C; van de Warrenburg BP; Orsi L; Giunti P; Filla A; Szymanski S; Klockgether T; Berciano J; Pandolfo M; Boesch S; Melegh B; Timmann D; Mandich P; Camuzat A; Goto J; Ashizawa T; Cazeneuve C; Tsuji S; Pulst SM; Brusco A; et alii...

Frontotemporal dementia and its subtypes: a genome-wide association study. in The Lancet. Neurology / Lancet Neurol. 2014 Jul;13(7):686-99. doi: 10.1016/S1474-4422(14)70065-1.
2014
AOU Città della Salute di Torino

Ferrari R; Hernandez DG; Nalls MA; Rohrer JD; Ramasamy A; Kwok JB; Dobson-Stone C; Brooks WS; Schofield PR; Halliday GM; Hodges JR; Piguet O; Bartley L; Thompson E; Haan E; Hernández I; Ruiz A; Boada M; Borroni B; Padovani A; Cruchaga C; Cairns NJ; Benussi L; Binetti G; Ghidoni R; Forloni G; Galimberti D; Fenoglio C; Serpente M; et alii...

ELOVL5 mutations cause spinocerebellar ataxia 38. in American journal of human genetics / Am J Hum Genet. 2014 Aug 7;95(2):209-17. doi: 10.1016/j.ajhg.2014.07.001. Epub 2014 Jul 24.
2014
AOU San Luigi di Orbassano
AOU Città della Salute di Torino

Boccone L; Caruso D; Funaro A; Tempia F; Brice A; Durr A; Maillet-Vioud M; Giunti P; Padovani A; Costanzi C; Deleuze JF; Imbert J; Papotti MG; Orsi L; Duregon E; Couarch P; Vaula G; Tesson C; Moon YA; Mitro N; Hoxha E; Mura I; Coviello DA; Calcia A; Gaussen M; Mancini C; Ragusa N; Borroni B; Giorgio E; et alii...