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Saccà Francesco
Saccà Francesco
Assistant Professor of Neurology - University Federico II Naples
在 unina.it 的电子邮件经过验证
标题
引用次数
引用次数
年份
Siponimod versus placebo in secondary progressive multiple sclerosis (EXPAND): a double-blind, randomised, phase 3 study
L Kappos, A Bar-Or, BAC Cree, RJ Fox, G Giovannoni, R Gold, ...
The Lancet 391 (10127), 1263-1273, 2018
9842018
Safety and efficacy of eculizumab in anti-acetylcholine receptor antibody-positive refractory generalised myasthenia gravis (REGAIN): a phase 3, randomised, double-blind …
JF Howard, K Utsugisawa, M Benatar, H Murai, RJ Barohn, I Illa, S Jacob, ...
The Lancet Neurology 16 (12), 976-986, 2017
6012017
Safety, efficacy, and tolerability of efgartigimod in patients with generalised myasthenia gravis (ADAPT): a multicentre, randomised, placebo-controlled, phase 3 trial
JF Howard, V Bril, T Vu, C Karam, S Peric, T Margania, H Murai, ...
The Lancet Neurology 20 (7), 526-536, 2021
3052021
Long‐term safety and efficacy of eculizumab in generalized myasthenia gravis
S Muppidi, K Utsugisawa, M Benatar, H Murai, RJ Barohn, I Illa, S Jacob, ...
Muscle & nerve 60 (1), 14-24, 2019
1932019
SCA Functional Index: a useful compound performance measure for spinocerebellar ataxia
T Schmitz-Hubsch, P Giunti, DA Stephenson, C Globas, L Baliko, F Saccà, ...
Neurology 71 (7), 486-492, 2008
1602008
Cognitive impairment at diagnosis predicts 10-year multiple sclerosis progression
M Moccia, R Lanzillo, R Palladino, KCM Chang, T Costabile, C Russo, ...
Multiple Sclerosis Journal 22 (5), 659-667, 2016
1592016
A genome-wide association meta-analysis identifies a novel locus at 17q11. 2 associated with sporadic amyotrophic lateral sclerosis
I Fogh, A Ratti, C Gellera, K Lin, C Tiloca, V Moskvina, L Corrado, ...
Human molecular genetics 23 (8), 2220-2231, 2014
1402014
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study
C Criscuolo, L Chessa, S Di Giandomenico, P Mancini, F Saccà, ...
Neurology 66 (8), 1207-1210, 2006
1342006
Dimethyl fumarate mediates Nrf2-dependent mitochondrial biogenesis in mice and humans
G Hayashi, M Jasoliya, S Sahdeo, F Saccà, C Pane, A Filla, A Marsili, ...
Human molecular genetics 26 (15), 2864-2873, 2017
1092017
Fingolimod versus interferon beta/glatiramer acetate after natalizumab suspension in multiple sclerosis
P Iaffaldano, G Lucisano, C Pozzilli, V Brescia Morra, A Ghezzi, ...
Brain 138 (11), 3275-3286, 2015
852015
A combined nucleic acid and protein analysis in Friedreich ataxia: implications for diagnosis, pathogenesis and clinical trial design
F Sacca, G Puorro, A Antenora, A Marsili, A Denaro, R Piro, P Sorrentino, ...
PLoS One 6 (3), e17627, 2011
792011
Long‐term safety and efficacy of Eculizumab in Aquaporin‐4 IgG‐positive NMOSD
DM Wingerchuk, K Fujihara, J Palace, A Berthele, M Levy, HJ Kim, ...
Annals of neurology 89 (6), 1088-1098, 2021
762021
Vascular smooth muscle cell dysfunction in patients with migraine
R Napoli, V Guardasole, E Zarra, M Matarazzo, C D'Anna, F Saccà, ...
Neurology 72 (24), 2111-2114, 2009
762009
Recombinant human erythropoietin increases frataxin protein expression without increasing mRNA expression
F Acquaviva, I Castaldo, A Filla, M Giacchetti, D Marmolino, A Monticelli, ...
The Cerebellum 7, 360-365, 2008
712008
Assessing association of comorbidities with treatment choice and persistence in MS: a real-life multicenter study
A Laroni, A Signori, GT Maniscalco, R Lanzillo, CV Russo, E Binello, ...
Neurology 89 (22), 2222-2229, 2017
682017
The EDSS integration with the Brief International Cognitive Assessment for Multiple Sclerosis and orientation tests
F Saccà, T Costabile, A Carotenuto, R Lanzillo, M Moccia, C Pane, ...
Multiple Sclerosis Journal 23 (9), 1289-1296, 2017
682017
Multiple hormone deficiencies in chronic heart failure
M Arcopinto, A Salzano, E Bossone, F Ferrara, E Bobbio, D Sirico, O Vriz, ...
International Journal of Cardiology 184, 421-423, 2015
652015
A gene expression phenotype in lymphocytes from Friedreich ataxia patients
G Coppola, R Burnett, S Perlman, R Versano, F Gao, H Plasterer, M Rai, ...
Annals of neurology 70 (5), 790-804, 2011
632011
Novel mutation of SACS gene in a Spanish family with autosomal recessive spastic ataxia
C Criscuolo, F Saccà, G De Michele, P Mancini, O Combarros, J Infante, ...
Movement Disorders: Official Journal of the Movement Disorder Society 20 (10 …, 2005
632005
Early and unrestricted access to high-efficacy disease-modifying therapies: a consensus to optimize benefits for people living with multiple sclerosis
M Filippi, R Danesi, T Derfuss, M Duddy, P Gallo, R Gold, EK Havrdová, ...
Journal of neurology, 1-8, 2022
622022
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