Sfoglia per AUTORE
DE MARCO G
Collezione AOU Città della Salute di Torino

  

Items : 12

Brain Metabolic Features of FUS-ALS: A 2-[(18)F]FDG-PET Study. in Annals of neurology / Ann Neurol. 2025 Feb 20. doi: 10.1002/ana.27201.
2025
AOU Città della Salute di Torino

Canosa A; Manera U; Vasta R; Zocco G; Di Pede F; Cabras S; De Mattei F; Palumbo F; Iazzolino B; Minerva E; Sbaiz L; Brunetti M; Gallone S; Grassano M; Matteoni E; Polverari G; Fuda G; Casale F; Salamone P; De Marco G; Marchese G; Moglia C; Calvo A; Pagani M; Chiò A;

Presymptomatic geographical distribution of ALS patients suggests the involvement of environmental factors in the disease pathogenesis. in Journal of neurology / J Neurol. 2023 Nov;270(11):5475-5482. doi: 10.1007/s00415-023-11888-8. Epub 2023 Jul 25.
2023
AOU Città della Salute di Torino
AOU Novara

Calvo A; Chiò A; Manera U; De Marchi F; Moglia C; Mazzini L; Canosa A; Palumbo F; Fuda G; Marchese G; De Marco G; Bombaci A; Grassano M; De Mattei F; Matteoni E; Di Pede F; Sgambetterra S; Cabras S; Callegaro S; Vasta R;

SOMAscan Proteomics Identifies Novel Plasma Proteins in Amyotrophic Lateral Sclerosis Patients. in International journal of molecular sciences / Int J Mol Sci. 2023 Jan 18;24(3):1899. doi: 10.3390/ijms24031899.
2023
ASL Torino 4
AOU Città della Salute di Torino

Chiò A; Caramelli M; De Marco G; Tessarolo C; D'Angelo A; Carta V; Testori C; Crociara P; Manera U; Favole A; Casale F; Calvo A; Gallo M; Palmitessa C; Benedetti V; Guana F; Chiorino G; Berrone E; Casalone C; Corona C;

Shared and Unique Disease Pathways in Amyotrophic Lateral Sclerosis and Parkinson's Disease Unveiled in Peripheral Blood Mononuclear Cells. in ACS chemical neuroscience / ACS Chem Neurosci. 2023 Dec 6;14(23):4240-4251. doi: 10.1021/acschemneuro.3c00629. Epub 2023 Nov 8.
2023
ASL Vercelli
AOU Città della Salute di Torino

Lopiano L; Chiò A; Comi C; Fuda G; Moglia C; De Marco G; Calvo A; Colugnat I; Monti C; Zibetti M; Rizzone MG; Casale F; Lualdi M; Fasano M; Alberio T;

Phenotype Analysis of Fused in Sarcoma Mutations in Amyotrophic Lateral Sclerosis. in Neurology. Genetics / Neurol Genet. 2022 Sep 12;8(5):e200011. doi: 10.1212/NXG.0000000000200011. eCollection 2022 Oct.
2022
AOU Città della Salute di Torino

Grassano M; Brodini G; De Marco G; Casale F; Fuda G; Salamone P; Brunetti M; Sbaiz L; Gallone S; Cugnasco P; Bombaci A; Vasta R; Manera U; Canosa A; Moglia C; Calvo A; Traynor BJ; Chio A;

Effects of intracellular calcium accumulation on proteins encoded by the major genes underlying amyotrophic lateral sclerosis. in Scientific reports / Sci Rep. 2022 Jan 10;12(1):395. doi: 10.1038/s41598-021-04267-8.
2022
AOU Città della Salute di Torino

De Marco G; Lomartire A; Manera U; Canosa A; Grassano M; Casale F; Fuda G; Salamone P; Rinaudo MT; Colombatto S; Moglia C; Chiò A; Calvo A;

A novel splice site FUS mutation in a familial ALS case: effects on protein expression. in Amyotrophic lateral sclerosis & frontotemporal degeneration / Amyotroph Lateral Scler Frontotemporal Degener. 2022 Feb;23(1-2):128-136. doi: 10.1080/21678421.2021
2022
AOU Città della Salute di Torino

Chiò A; Calvo A; Moglia C; Gallone S; Sbaiz L; Fuda G; Salamone P; Vasta R; Manera U; Brunetti M; Grassano M; De Marco G; Lomartire A; Canosa A;

The heterozygous deletion c.1509_1510delAG in exon 14 of FUS causes an aggressive childhood-onset ALS with cognitive impairment. in Neurobiology of aging / Neurobiol Aging. 2021 Jul;103:130.e1-130.e7. doi: 10.1016/j.neurobiolaging.2021.01.029. Epub 2021 Fe
2021
AOU Città della Salute di Torino

Chiò A; Origone P; Calvo A; Moglia C; Vasta R; Manera U; Sansone VA; Lunetta C; Rinaudo MT; Albamonte E; Lomartire A; Canosa A; De Marco G; Lanteri P; Meola I; Mandich P;

A familial amyotrophic lateral sclerosis pedigree discordant for a novel p.Glu46Asp heterozygous OPTN variant and the p.Ala5Val heterozygous SOD1 missense mutation. in Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia / J Clin Neurosci. 2020 May;75:223-225. doi: 10.1016/j.jocn.2020.03.032. Epub 2020 Mar 27.
2020
AOU Città della Salute di Torino

Moglia C; Chiò A; Calvo A; De Marco G; Cammarosano S; Vasta R; Brunetti M; Manera U; Grassano M; Barberis M; Canosa A;

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...

Monocytes of patients with amyotrophic lateral sclerosis linked to gene mutations display altered TDP-43 subcellular distribution. in Neuropathology and applied neurobiology / Neuropathol Appl Neurobiol. 2017 Feb;43(2):133-153. doi: 10.1111/nan.12328. Epub 2016 Jun 28.
2017
AOU Città della Salute di Torino

Tarella C; Fini N; Restagno G; Moglia C; Canosa A; Manera U; Borghero G; Caponnetto C; Mandrioli J; De Luca E; Mostert M; Risso A; Lomartire A; Calvo A; De Marco G; Giordana MT; Rinaudo MT; Chiò A;

Reduced cellular Ca(2+) availability enhances TDP-43 cleavage by apoptotic caspases. in Biochimica et biophysica acta / Biochim Biophys Acta. 2014 Apr;1843(4):725-34. doi: 10.1016/j.bbamcr.2014.01.010. Epub 2014 Jan 16.
2014
AOU Città della Salute di Torino

De Marco G; Lomartire A; Mandili G; Lupino E; Buccinnà B; Ramondetti C; Moglia C; Novelli F; Piccinini M; Mostert M; Rinaudo MT; Chiò A; Calvo A;