mario sabatelli
mario sabatelli
Catholic University of Rome
Verified email at unicatt.it
TitleCited byYear
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
AE Renton, E Majounie, A Waite, J Simón-Sánchez, S Rollinson, ...
Neuron 72 (2), 257-268, 2011
27992011
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
9682010
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
7402012
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, 2014
2662014
The prognosis and main prognostic indicators of Guillain-Barre syndrome A multicentre prospective study of 297 patients
Italian Guillain-Barré Study Group
Brain 119 (6), 2053-2061, 1996
1841996
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72
A Chị, G Borghero, G Restagno, G Mora, C Drepper, BJ Traynor, ...
Brain 135 (3), 784-793, 2012
1642012
Intravenous immunoglobulin versus intravenous methylprednisolone for chronic inflammatory demyelinating polyradiculoneuropathy: a randomised controlled trial
E Nobile-Orazio, D Cocito, S Jann, A Uncini, E Beghi, P Messina, ...
The Lancet Neurology 11 (6), 493-502, 2012
1362012
CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis
V Fridman, B Bundy, MM Reilly, D Pareyson, C Bacon, J Burns, J Day, ...
J Neurol Neurosurg Psychiatry 86 (8), 873-878, 2015
1332015
Autosornal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: Clinical, electrophysiologic, and genetic aspects of a large family
A Quattrone, A Gambardella, F Bono, U Aguglia, A Bolino, AC Bruni, ...
Neurology 46 (5), 1318-1318, 1996
1261996
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation
A Chị, G Restagno, M Brunetti, I Ossola, A Calvo, G Mora, M Sabatelli, ...
Neurobiology of aging 30 (8), 1272-1275, 2009
1242009
Randomised controlled trial of methotrexate for chronic inflammatory demyelinating polyradiculoneuropathy (RMC trial): a pilot, multicentre study
RMC Trial Group
The Lancet Neurology 8 (2), 158-164, 2009
1242009
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis
A Chị, JC Schymick, G Restagno, SW Scholz, F Lombardo, SL Lai, ...
Human molecular genetics 18 (8), 1524-1532, 2009
1172009
Heterogeneity of root and nerve ultrasound pattern in CIDP patients
L Padua, G Granata, M Sabatelli, M Inghilleri, M Lucchetta, M Luigetti, ...
Clinical Neurophysiology 125 (1), 160-165, 2014
1062014
Pure motor chronic inflammatory demyelinating polyneuropathy
M Sabatelli, F Madia, T Mignogna, G Lippi, L Quaranta, P Tonali
Journal of neurology 248 (9), 772-777, 2001
992001
Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease
S Lattante, A Conte, M Zollino, M Luigetti, A Del Grande, G Marangi, ...
Neurology 79 (1), 66-72, 2012
952012
Lithium carbonate in amyotrophic lateral sclerosis: lack of efficacy in a dose-finding trial
A Chị, G Borghero, A Calvo, M Capasso, C Caponnetto, M Corbo, ...
Neurology 75 (7), 619-625, 2010
912010
Rituximab in patients with chronic inflammatory demyelinating polyradiculoneuropathy: a report of 13 cases and review of the literature
L Benedetti, C Briani, D Franciotta, R Fazio, I Paolasso, C Comi, ...
Journal of Neurology, Neurosurgery & Psychiatry 82 (3), 306-308, 2011
882011
FUS mutations in sporadic amyotrophic lateral sclerosis
SL Lai, Y Abramzon, JC Schymick, DA Stephan, T Dunckley, A Dillman, ...
Neurobiology of aging 32 (3), 550. e1-550. e4, 2011
842011
An ALS-associated mutation in the FUS 3′-UTR disrupts a microRNA–FUS regulatory circuitry
SD Modigliani, M Morlando, L Errichelli, M Sabatelli, I Bozzoni
Nature communications 5, 4335, 2014
802014
Botulinum toxin A versus B in sialorrhea: a prospective, randomized, double‐blind, crossover pilot study in patients with amyotrophic lateral sclerosis or Parkinson's disease
A Guidubaldi, A Fasano, T Ialongo, C Piano, M Pompili, R Mascianà, ...
Movement disorders 26 (2), 313-319, 2011
802011
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