Sfoglia per AUTORE
CROCE R
Collezione AOU Novara
Items : 3
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
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;
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
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;
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
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;