Sfoglia per AUTORE
ANDERSEN PM
Collezione AOU Città della Salute di Torino

  

Items : 11

2024
AOU Città della Salute di Torino

Tysnes OB; Silani V; Reviers E; Salachas F; Probyn K; Petri S; Mora JS; McDermott CJ; Ludolph A; Ku?ma-Kozakiewicz M; Hardiman O; De Carvalho M; Couratier P; Chiò A; Andersen PM; Al-Chalabi A; Van Damme P; van den Berg LH; Villanueva G; Weber M;

Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosis. in Neurobiology of aging / Neurobiol Aging. 2023 Feb;122:76-87. doi: 10.1016/j.neurobiolaging.2022.11.010. Epub 2022 Nov 17.
2023
AOU Città della Salute di Torino

Weber M; Andersen PM; Neuwirth C; de Carvalho M; Van Damme P; Hardiman O; McLaughlin RL; Chio A; Al-Chalabi A; Pardina JSM; Ravits J; Nordin A; Canosa A; Brunetti M; Moglia C; Calvo A; Dooijes D; Moisse M; van Eijk KR; Gijzen M; Kool L; van Rheenen W; van Vugt JJFA; Seelen M; Hop PJ; Tazelaar GHP; van den Berg LH; Veldink JH; van Es MA; et alii...

Clinical trials in pediatric ALS: a TRICALS feasibility study. in Amyotrophic lateral sclerosis & frontotemporal degeneration / Amyotroph Lateral Scler Frontotemporal Degener. 2022 Nov;23(7-8):481-488. doi: 10.1080/21678421.2021
2022
AOU Città della Salute di Torino

Stevic Z; SorarÙ G; Sarafov S; Salachas F; Rubio MÁ; Roes KCB; Riva N; Reviers E; Povedano M; Petri S; Mora JS; Mcdermott CJ; Meyer T; Mandrioli J; Lunetta C; Leigh PN; Lambert T; Kuzma-Kozakiewicz M; Koritnik B; Ingre C; HØyer H; HolmØy T; Hanemann CO; Grosskreutz J; GarcÍa Redondo A; Filosto M; Esteban J; Van Es MA; Desnuelle C; et alii...

The importance of offering early genetic testing in everyone with amyotrophic lateral sclerosis. in Brain : a journal of neurology / Brain. 2022 May 24;145(4):1207-1210. doi: 10.1093/brain/awab472.
2022
AOU Città della Salute di Torino

Salmon K; Kiernan MC; Kim SH; Andersen PM; Chio A; van den Berg LH; Van Damme P; Al-Chalabi A; Lillo P; Andrews JA; Genge A;

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...

Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS. in Science translational medicine / Sci Transl Med. 2022 Feb 23;14(633):eabj0264. doi: 10.1126/scitranslmed.abj0264. Epub 2022 Feb 23.
2022
AOU Città della Salute di Torino

Hop PJ; Zwamborn RAJ; Hannon E; Shireby GL; Nabais MF; Walker EM; van Rheenen W; van Vugt JJFA; Dekker AM; Westeneng HJ; Tazelaar GHP; van Eijk KR; Moisse M; Baird D; Al Khleifat A; Iacoangeli A; Ticozzi N; Ratti A; Cooper-Knock J; Morrison KE; Shaw PJ; Basak AN; Chiò A; Calvo A; Moglia C; Canosa A; Brunetti M; Grassano M; Gotkine M; 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...

A novel p.Ser108LeufsTer15 SOD1 mutation leading to the formation of a premature stop codon in an apparently sporadic ALS patient: insights into the underlying pathomechanisms. in Neurobiology of aging / Neurobiol Aging. 2018 Dec;72:189.e11-189.e17. doi: 10.1016/j.neurobiolaging.2018.08.014. Epub 2018 A
2018
AOU Città della Salute di Torino

Canosa A; De Marco G; Lomartire A; Rinaudo MT; Di Cunto F; Turco E; Barberis M; Brunetti M; Casale F; Moglia C; Calvo A; Marklund SL; Andersen PM; Mora G; Chiò A; Canosa A; De Marco G; Lomartire A; Rinaudo MT; Di Cunto F; Turco E; Barberis M; Brunetti M; Casale F; Moglia C; Calvo A; Marklund SL; Andersen PM; Mora G; 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...

Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis. in JAMA neurology / JAMA Neurol. 2016 Jul 1;73(7):812-20. doi: 10.1001/jamaneurol.2016.1114.
2016
AOU Città della Salute di Torino
AOU Novara

Shaw CE; van den Berg LH; Lewis CM; Hardiman O; Landers JE; Brown RH; Robberecht W; Van Damme P; D'Alfonso S; Traynor BJ; Mazzini L; Ticozzi N; Comi GP; Andersen PM; Leigh PN; Shaw PJ; Morrison KE; Melki J; Meininger V; van Rheenen W; Topp S; Smith BN; Dobson R; Glass JD; Newhouse S; Castellotti B; Cereda C; Del Bo R; Stahl D; et alii...

Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study. in Neurobiology of aging / Neurobiol Aging. 2014 Oct;35(10):2420.e13-4. doi: 10.1016/j.neurobiolaging.2014.04.014. Epub 2014 Ap
2014
AOU Città della Salute di Torino
AOU Novara

Hardiman O; Cronin S; Andersen PM; D'Alfonso S; Fogh I; Shatunov A; Robberecht W; van Damme P; Goris A; Ludolph AC; Waibel S; Meyer T; Corti S; Del Bo R; Mazzini L; Groen EJ; Corrado L; van Vught PW; Blauw HM; van Es MA; Saris CG; Lemmens R; Birve A; Traynor BJ; Restagno G; Mora G; Calvo A; Taroni F; Chiò A; et alii...