Sfoglia per AUTORE
CORRADO L
Collezione AOU Novara

  

Items : 22

A Novel GBF1 Variant in a Charcot-Marie-Tooth Type 2: Insights from Familial Analysis. in Genes / Genes (Basel). 2024 Nov 29;15(12):1556. doi: 10.3390/genes15121556.
2024
AOU Novara

Ciampana V; Corrado L; Magistrelli L; Contaldi E; Comi C; D'Alfonso S; Vecchio D;

Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data. in Cell genomics / Cell Genom. 2024 Nov 13;4(11):100679. doi: 10.1016/j.xgen.2024.100679. Epub 2024 Oct 21.
2024
AOU Città della Salute di Torino
AOU Novara

Silani V; Siciliano G; Nath A; Wang T; Pasternack N; Doucet-O'Hare T; Johnson K; Gellera C; Ratti A; Pal S; Chandran S; D'Alfonso S; Cereda C; Sorarù G; Hardiman O; McLaughlin R; Al-Chalabi A; van den Berg LH; Scholz SW; Dalgard CL; Dobson RJB; Breen G; Shaw PJ; Cooper-Knock J; Morrison KE; Patel H; Chung R; Lee SH; Curtis CJ; et alii...

Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis. in Neurology / Neurology. 2023 Jul 4;101(1):e83-e93. doi: 10.1212/WNL.0000000000207367. Epub 2023 May 18.
2023
AOU Città della Salute di Torino
AOU Novara

Calvo A; Mazzini L; D'Alfonso S; Corrado L; Traynor BJ; Peotta L; Iazzolino B; Mora G; Chia R; Dalgard C; De Marchi F; Barberis M; Brunetti M; Gallone S; Palumbo F; Vasta R; Grassano M; Manera U; Canosa A; Moglia C; Chiò A;

Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral Sclerosis. in Neurology. Genetics / Neurol Genet. 2022 Oct 26;8(6):e200033. doi: 10.1212/NXG.0000000000200033. eCollection 2022 Dec.
2022
AOU Città della Salute di Torino
AOU Novara

Chio A; Traynor BJ; Mazzini L; Dalfonso S; Corrado L; Chia R; Scholz SW; Dalgard C; Pagani M; Arena V; De Marchi F; Brunetti M; Gallone S; Cugnasco P; Palumbo F; Grassano M; Vasta R; Manera U; Moglia C; Canosa A; Calvo A;

Exploring the phenotype of Italian patients with ALS with intermediate ATXN2 polyQ repeats. in Journal of neurology, neurosurgery, and psychiatry / J Neurol Neurosurg Psychiatry. 2022 Aug 25;93(11):1216-20. doi: 10.1136/jnnp-2022-329376.
2022
AOU Città della Salute di Torino
AOU Novara

Corrado L; Traynor B; Peotta L; Iazzolino B; Mora G; Chia R; Dalgard C; De Marchi F; Barberis M; Brunetti M; Gallone S; Palumbo F; Vasta R; Grassano M; Canosa A; Manera U; Moglia C; Chio A; D'Alfonso S; Mazzini L; Calvo A;

Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients. in Antioxidants (Basel, Switzerland) / Antioxidants (Basel). 2022 Apr 22;11(5):815. doi: 10.3390/antiox11050815.
2022
AOU Novara

Perciballi E; Bovio F; Rosati J; Arrigoni F; D'Anzi A; Lattante S; Gelati M; De Marchi F; Lombardi I; Ruotolo G; Forcella M; Mazzini L; D'Alfonso S; Corrado L; Sabatelli M; Conte A; De Gioia L; Martino S; Vescovi AL; Fusi P; Ferrari D;

Clinical relevance of single-subject brain metabolism patterns in amyotrophic lateral sclerosis mutation carriers. in NeuroImage. Clinical / Neuroimage Clin. 2022;36:103222. doi: 10.1016/j.nicl.2022.103222. Epub 2022 Oct 5.
2022
ASL Vercelli
AOU Novara

Perani D; Sacchetti GM; Cantello R; D'Alfonso S; Matheoud R; Corrado L; Sarnelli MF; Caminiti SP; Mazzini L; Tondo G; Comi C; De Marchi F;

C9ORF72 Repeat Expansion Affects the Proteome of Primary Skin Fibroblasts in ALS. in International journal of molecular sciences / Int J Mol Sci. 2021 Sep 27;22(19):10385. doi: 10.3390/ijms221910385.
2021
AOU Novara

Lualdi M; Shafique A; Pedrini E; Pieroni L; Greco V; Castagnola M; Cucina G; Corrado L; Di Pierro A; De Marchi F; Camillo L; Colombrita C; D'Anca M; Alberio T; D'Alfonso S; Fasano M;

2021
AOU Novara

Barizzone N; Cagliani R; Basagni C; Clarelli F; Mendozzi L; Agliardi C; Forni D; Tosi M; Mascia E; Favero F; Corà D; Corrado L; Sorosina M; Esposito F; Zuccalà M; Vecchio D; Liguori M; Comi C; Comi G; Martinelli V; Filippi M; Leone M; Martinelli-Boneschi F; Caputo D; Sironi M; Guerini FR; D'Alfonso S;

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...

Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series. in Neurogenetics / Neurogenetics. 2021 Mar;22(1):65-70. doi: 10.1007/s10048-021-00634-9. Epub 2021 Jan 20.
2021
ASL Novara
AOU Novara

Mazzini L; D'Alfonso S; Comi C; Garavaglia B; Cantello R; Invernizzi F; Nasuelli N; Carecchio M; Basagni C; De Marchi F; Croce R; Magistrelli L; Corrado L;

Variants in the 5'UTR reduce SHOX expression and contribute to SHOX haploinsufficiency. in European journal of human genetics : EJHG / Eur J Hum Genet. 2021 Jan;29(1):110-121. doi: 10.1038/s41431-020-0676-y. Epub 2020 Jul 9.
2021
AOU Città della Salute di Torino
AOU Novara

Prodam F; De Sanctis L; Stuppia L; Monzani A; Vinci G; Bellone S; Grandone A; Corrado L; Essa WA; Baffico AM; Mellone S; Fanelli A; Vannelli S; Babu D; Giordano M;

The first case of the TARDBP p.G294V mutation in a homozygous state: is a single pathogenic allele sufficient to cause ALS? in Amyotrophic lateral sclerosis & frontotemporal degeneration / Amyotroph Lateral Scler Frontotemporal Degener. 2020 May;21(3-4):273-279. doi: 10.1080/21678421.2019
2020
AOU Novara

Corrado L; Pensato V; Croce R; Di Pierro A; Mellone S; Dalla Bella E; Salsano E; Paraboschi EM; Giordano M; Saraceno M; Mazzini L; Gellera C; D'Alfonso S;

Regional spreading of symptoms at diagnosis as a prognostic marker in amyotrophic lateral sclerosis: a population-based study. in Journal of neurology, neurosurgery, and psychiatry / J Neurol Neurosurg Psychiatry. 2020 Mar;91(3):291-297. doi: 10.1136/jnnp-2019-321153. Epub 2019 Dec
2020
AOU Novara

Manera U; Calvo A; Daviddi M; Canosa A; Vasta R; Torrieri MC; Grassano M; Brunetti M; D'Alfonso S; Corrado L; De Marchi F; Moglia C; D'Ovidio F; Mora G; Mazzini L; Chiò A;

Analysis of the GCG repeat length in NIPA1 gene in C9orf72-mediated ALS in a large Italian ALS cohort. in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology / Neurol Sci. 2019 Dec;40(12):2537-2540. doi: 10.1007/s10072-019-04001-3. Epub 2019 Jul 9.
2019
AOU Città della Salute di Torino
AOU Novara

Mazzini L; Moglia C; Calvo A; Barizzone N; Zuccalà M; De Marchi F; Bersano E; Croce R; Barberis M; Di Pierro A; Brunetti M; Corrado L; Chiò A; D'Alfonso S;

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene. in Neuron / Neuron. 2018 Mar 21;97(6):1267-1288. doi: 10.1016/j.neuron.2018.02.027.
2018
AOU Novara

Nicolas A; Kenna KP; Renton AE; Ticozzi N; Faghri F; Chia R; Dominov JA; Kenna BJ; Nalls MA; Keagle P; Rivera AM; van Rheenen W; Murphy NA; van Vugt JJFA; Geiger JT; Van der Spek RA; Pliner HA; Shankaracharya; Smith BN; Marangi G; Topp SD; Abramzon Y; Gkazi AS; Eicher JD; Kenna A; Mora G; Calvo A; Mazzini L; Riva N; et alii...

Ptosis and bulbar onset: an unusual phenotype of familial ALS? in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology / Neurol Sci. 2018 Feb;39(2):377-378. doi: 10.1007/s10072-017-3186-0. Epub 2017 Nov 13.
2018
AOU Novara

De Marchi F; Corrado L; Bersano E; Sarnelli MF; Solara V; D'Alfonso S; Cantello R; Mazzini L;

Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases. in Amyotrophic lateral sclerosis & frontotemporal degeneration / Amyotroph Lateral Scler Frontotemporal Degener. 2018 Aug;19(5-6):426-431. doi: 10.1080/21678421.2018
2018
AOU Novara

Corrado L; Tiloca C; Locci C; Bagarotti A; Hamzeiy H; Colombrita C; De Marchi F; Barizzone N; Cotella D; Ticozzi N; Mazzini L; Nazli Basak A; Ratti A; Silani V; D'alfonso S;

The Length of SNCA Rep1 Microsatellite May Influence Cognitive Evolution in Parkinson's Disease. in Frontiers in neurology / Front Neurol. 2018 Mar 29;9:213. doi: 10.3389/fneur.2018.00213. eCollection 2018.
2018
AOU Città della Salute di Torino
AOU Novara

Pacchetti C; Bono G; Comi GP; Magnani C; D'Alfonso S; Cereda C; Zangaglia R; Trezzi I; Locci C; Di Fonzo A; Riboldazzi G; Tesei S; Magistrelli L; Carecchio M; Oggioni GD; Tunesi S; De Marchi F; Corrado L; Cantello R; Goldwurm S; Comi C;

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...

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...

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...

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