Corrado Angelini
Corrado Angelini
IRCCS S.Camillo Hospital
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Cited by
Cited by
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
J Liu, M Aoki, I Illa, C Wu, M Fardeau, C Angelini, C Serrano, ...
Nature genetics 20 (1), 31-36, 1998
Carnitine deficiency of human skeletal muscle with associated lipid storage myopathy: a new syndrome
AG Engel, C Angelini
Science 179 (4076), 899-902, 1973
MELAS: clinical features, biochemistry, and molecular genetics
E Ciafaloni, E Ricci, S Shanske, CT Moraes, G Silvestri, M Hirano, ...
Annals of Neurology: Official Journal of the American Neurological …, 1992
Assessment of mitochondrial respiratory chain enzymatic activities on tissues and cultured cells
M Spinazzi, A Casarin, V Pertegato, L Salviati, C Angelini
Nature protocols 7 (6), 1235-1246, 2012
β–sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex
CG Bönnemann, R Modi, S Noguchi, Y Mizuno, M Yoshida, E Gussoni, ...
Nature genetics 11 (3), 266-273, 1995
Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies.
AH Beggs, EP Hoffman, JR Snyder, K Arahata, L Specht, F Shapiro, ...
American journal of human genetics 49 (1), 54, 1991
Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q
J Melki, S Abdelhak, P Sheth, MF Bachelot, P Burlet, A Marcadet, J Aicardi, ...
Nature 344 (6268), 767-768, 1990
Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb–MyoD pathways in muscle regeneration
M Bakay, Z Wang, G Melcon, L Schiltz, J Xuan, P Zhao, V Sartorelli, J Seo, ...
Brain 129 (4), 996-1013, 2006
Improved diagnosis of Becker muscular dystrophy by dystrophin testing
EP Hoffman, LM Kunkel, C Angelini, A Clarke, M Johnson, JB Harris
Neurology 39 (8), 1011-1011, 1989
Systemic carnitine deficiency—a treatable inherited lipid-storage disease presenting as Reye's syndrome
PR Chapoy, C Angelini, WJ Brown, JE Stiff, AL Shug, SD Cederbaum
New England Journal of Medicine 303 (24), 1389-1394, 1980
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
Increases in walking distance in patients with peripheral vascular disease treated with L-carnitine: a double-blind, cross-over study.
G Brevetti, M Chiariello, G Ferulano, A Policicchio, E Nevola, A Rossini, ...
Circulation 77 (4), 767-773, 1988
Correlating phenotype and genotype in the periodic paralyses
TM Miller, MRD Da Silva, HA Miller, H Kwiecinski, JR Mendell, R Tawil, ...
Neurology 63 (9), 1647-1655, 2004
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
Cerebellar ataxia and coenzyme Q10 deficiency
C Lamperti, A Naini, M Hirano, DC De Vivo, E Bertini, S Servidei, ...
Neurology 60 (7), 1206-1208, 2003
Survival motor-neuron gene transcript analysis in muscles from spinal muscular-atrophy patients
M Gennarelli, M Lucarelli, F Capon, A Pizzuti, L Merlini, C Angelini, ...
Biochemical and biophysical research communications 213 (1), 342-348, 1995
Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation
J Wang, E Pegoraro, E Menegazzo, M Gennarelli, RC Hoop, C Angelini, ...
Human molecular genetics 4 (4), 599-606, 1995
The role of corticosteroids in muscular dystrophy: a critical appraisal
C Angelini
Muscle & Nerve: Official Journal of the American Association of …, 2007
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
Safety and efficacy of eculizumab in anti-acetylcholine receptor antibody-positive refractory generalised myasthenia gravis (REGAIN): a phase 3, randomised, double-blind …
JF Howard Jr, K Utsugisawa, M Benatar, H Murai, RJ Barohn, I Illa, ...
The Lancet Neurology 16 (12), 976-986, 2017
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