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Angela Lucia Berardinelli
Angela Lucia Berardinelli
Fond. Mondino
Verified email at unipv.it
Title
Cited by
Cited by
Year
Mutations in the sarcoglycan genes in patients with myopathy
DJ Duggan, JR Gorospe, M Fanin, EP Hoffman, C Angelini, E Pegoraro, ...
New England Journal of Medicine 336 (9), 618-625, 1997
2791997
A multicenter, double‐blind, randomized trial of deflazacort versus prednisone in Duchenne muscular dystrophy
MD Bonifati, G Ruzza, P Bonometto, A Berardinelli, K Gorni, S Orcesi, ...
Muscle & nerve 23 (9), 1344-1347, 2000
2622000
North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy
E Mazzone, D Martinelli, A Berardinelli, S Messina, A D’Amico, G Vasco, ...
Neuromuscular Disorders 20 (11), 712-716, 2010
2422010
Reliability of the North Star Ambulatory Assessment in a multicentric setting
ES Mazzone, S Messina, G Vasco, M Main, M Eagle, A D’Amico, L Doglio, ...
Neuromuscular Disorders 19 (7), 458-461, 2009
2342009
Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study
E Mazzone, G Vasco, MP Sormani, Y Torrente, A Berardinelli, S Messina, ...
Neurology 77 (3), 250-256, 2011
2292011
Effects of different ventilator settings on sleep and inspiratory effort in patients with neuromuscular disease
F Fanfulla, M Delmastro, A Berardinelli, NDA Lupo, S Nava
American journal of respiratory and critical care medicine 172 (5), 619-624, 2005
2032005
Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophy
E Mercuri, E Bertini, S Messina, A Solari, A D'amico, C Angelozzi, ...
Neurology 68 (1), 51-55, 2007
2022007
Autoantibodies to nodal isoforms of neurofascin in chronic inflammatory demyelinating polyneuropathy
E Delmont, C Manso, L Querol, A Cortese, A Berardinelli, A Lozza, ...
Brain 140 (7), 1851-1858, 2017
2002017
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study
E Mercuri, S Messina, C Bruno, M Mora, E Pegoraro, GP Comi, A D'Amico, ...
Neurology 72 (21), 1802-1809, 2009
1912009
Heart involvement in muscular dystrophies due to sarcoglycan gene mutations
P Melacini, M Fanin, DJ Duggan, MP Freda, A Berardinelli, GA Danieli, ...
Muscle & Nerve: Official Journal of the American Association of …, 1999
1761999
Attention deficit hyperactivity disorder and cognitive function in Duchenne muscular dystrophy: phenotype-genotype correlation
M Pane, ME Lombardo, P Alfieri, A D'Amico, F Bianco, G Vasco, G Piccini, ...
The Journal of pediatrics 161 (4), 705-709. e1, 2012
1722012
Muscle magnetic resonance imaging involvement in muscular dystrophies with rigidity of the spine
E Mercuri, E Clements, A Offiah, A Pichiecchio, G Vasco, F Bianco, ...
Annals of Neurology: Official Journal of the American Neurological …, 2010
1632010
Phenotypic clustering of lamin A/C mutations in neuromuscular patients
S Benedetti, I Menditto, M Degano, C Rodolico, L Merlini, A D’Amico, ...
Neurology 69 (12), 1285-1292, 2007
1632007
Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy.
R Tupler, A Berardinelli, L Barbierato, R Frants, JE Hewitt, G Lanzi, ...
Journal of medical genetics 33 (5), 366-370, 1996
1551996
Nonsense mutation in pseudouridylate synthase 1 (PUS1) in two brothers affected by myopathy, lactic acidosis and sideroblastic anaemia (MLASA)
E Fernandez-Vizarra, A Berardinelli, L Valente, V Tiranti, M Zeviani
Journal of medical genetics 44 (3), 173-180, 2007
1522007
24 month longitudinal data in ambulant boys with Duchenne muscular dystrophy
ES Mazzone, M Pane, MP Sormani, R Scalise, A Berardinelli, S Messina, ...
PloS one 8 (1), e52512, 2013
1442013
Antibodies to neurofascin, contactin-1, and contactin-associated protein 1 in CIDP: clinical relevance of IgG isotype
A Cortese, R Lombardi, C Briani, I Callegari, L Benedetti, F Manganelli, ...
Neurology: Neuroimmunology & Neuroinflammation 7 (1), e639, 2019
1422019
Long term natural history data in ambulant boys with Duchenne muscular dystrophy: 36-month changes
M Pane, ES Mazzone, S Sivo, MP Sormani, S Messina, A D′ Amico, ...
PLoS One 9 (10), e108205, 2014
1332014
Impaired muscle mitochondrial biogenesis and myogenesis in spinal muscular atrophy
M Ripolone, D Ronchi, R Violano, D Vallejo, G Fagiolari, E Barca, ...
JAMA neurology 72 (6), 666-675, 2015
1312015
Large-scale population analysis challenges the current criteria for the molecular diagnosis of fascioscapulohumeral muscular dystrophy
I Scionti, F Greco, G Ricci, M Govi, P Arashiro, L Vercelli, A Berardinelli, ...
The American Journal of Human Genetics 90 (4), 628-635, 2012
1242012
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