Seguir
Andrea Calvo
Andrea Calvo
Associate Professor of Neurology, 'Rita Levi Montalcini' Department of Neuroscience, University of
Dirección de correo verificada de unito.it
Título
Citado por
Citado por
Año
Exome sequencing reveals VCP mutations as a cause of familial ALS
JO Johnson, J Mandrioli, M Benatar, Y Abramzon, VM Van Deerlin, ...
Neuron 68 (5), 857-864, 2010
14452010
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
E Majounie, AE Renton, K Mok, EGP Dopper, A Waite, S Rollinson, ...
The Lancet Neurology 11 (4), 323-330, 2012
13242012
Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study
A Chiò, A Calvo, C Moglia, L Mazzini, G Mora
Journal of Neurology, Neurosurgery & Psychiatry 82 (7), 740-746, 2011
6092011
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
W Van Rheenen, A Shatunov, AM Dekker, RL McLaughlin, FP Diekstra, ...
Nature genetics 48 (9), 1043-1048, 2016
6032016
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1267-1288, 2018
5922018
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
JO Johnson, EP Pioro, A Boehringer, R Chia, H Feit, AE Renton, ...
Nature neuroscience 17 (5), 664-666, 2014
5212014
Projected increase in amyotrophic lateral sclerosis from 2015 to 2040
KC Arthur, A Calvo, TR Price, JT Geiger, A Chio, BJ Traynor
Nature communications 7 (1), 12408, 2016
4542016
Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model
HJ Westeneng, TPA Debray, AE Visser, RPA van Eijk, JPK Rooney, ...
The Lancet Neurology 17 (5), 423-433, 2018
4442018
Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling study
A Al-Chalabi, A Calvo, A Chio, S Colville, CM Ellis, O Hardiman, ...
The Lancet Neurology 13 (11), 1108-1113, 2014
4152014
SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
E Rubino, I Rainero, A Chiò, E Rogaeva, D Galimberti, P Fenoglio, ...
Neurology 79 (15), 1556-1562, 2012
3302012
Epidemiology of ALS in Italy: a 10-year prospective population-based study
A Chiò, G Mora, A Calvo, L Mazzini, E Bottacchi, R Mutani
Neurology 72 (8), 725-731, 2009
3202009
A longitudinal study on quality of life and depression in ALS patient–caregiver couples
A Gauthier, A Vignola, A Calvo, E Cavallo, C Moglia, L Sellitti, R Mutani, ...
Neurology 68 (12), 923-926, 2007
3122007
Caregiver burden and patients’ perception of being a burden in ALS
A Chio, A Gauthier, A Calvo, P Ghiglione, R Mutani
Neurology 64 (10), 1780-1782, 2005
3102005
Cognitive correlates in amyotrophic lateral sclerosis: a population-based study in Italy
A Montuschi, B Iazzolino, A Calvo, C Moglia, L Lopiano, G Restagno, ...
Journal of Neurology, Neurosurgery & Psychiatry 86 (2), 168-173, 2015
3072015
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
W Van Rheenen, RAA Van Der Spek, MK Bakker, JJFA Van Vugt, PJ Hop, ...
Nature genetics 53 (12), 1636-1648, 2021
2942021
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
KP Kenna, PTC Van Doormaal, AM Dekker, N Ticozzi, BJ Kenna, ...
Nature genetics 48 (9), 1037-1042, 2016
2912016
A cross sectional study on determinants of quality of life in ALS
A Chiò, A Gauthier, A Montuschi, A Calvo, N Di Vito, P Ghiglione, ...
Journal of Neurology, Neurosurgery & Psychiatry 75 (11), 1597-1601, 2004
2622004
Neuroimaging in amyotrophic lateral sclerosis: insights into structural and functional changes
A Chiò, M Pagani, F Agosta, A Calvo, A Cistaro, M Filippi
The Lancet Neurology 13 (12), 1228-1240, 2014
2382014
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72
A Chiò, G Borghero, G Restagno, G Mora, C Drepper, BJ Traynor, ...
Brain 135 (3), 784-793, 2012
2322012
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
R Chia, MS Sabir, S Bandres-Ciga, S Saez-Atienzar, RH Reynolds, ...
Nature genetics 53 (3), 294-303, 2021
2262021
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
Artículos 1–20