Corrado Angelini

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Eric P HoffmanProfessor, Department of Pharmaceutical Sciences, Binghamton UniversityCorreu electrònic verificat a binghamton.edu
Arianna PalmieriDipartimento FISPPA, Università degli Studi di PadovaCorreu electrònic verificat a unipd.it
Vincenzo NigroUniversità della Campania "Luigi Vanvitelli" Dipartimento di Medicina di Precisione, and TIGEMCorreu electrònic verificat a unicampania.it
VALENTINA PEGORAROIRCCS San Camillo Hospital, Venice, ItalyCorreu electrònic verificat a ospedalesancamillo.net
Giuseppe NovelliProfessore di Genetica Medica, Università di Roma Tor VergataCorreu electrònic verificat a med.uniroma2.it
Marco SpinazziCHU AngersCorreu electrònic verificat a chu-angers.fr
Serenella ServideiDipartimento di Neuroscienze, Università Cattolica del Sacro CuoreCorreu electrònic verificat a unicatt.it
Massimo GennarelliPhd, University of Brescia, IRCCS FatebenefratelliCorreu electrònic verificat a unibs.it
Olimpia Musumeciprofessor of Neurology , University of MessinaCorreu electrònic verificat a unime.it
Giacomo Pietro ComiProfessor of NeurologyCorreu electrònic verificat a unimi.it
Claudio SempliciniAzienda Ospedaliera Università di PadovaCorreu electrònic verificat a unipd.it
ENRICO BERTINIHead of the Research Unit of Neuromuscular and Neurodegenerative Disorders, Ospedale PediatricoCorreu electrònic verificat a opbg.net
David DugganTranslational Genomics Research InstituteCorreu electrònic verificat a tgen.org
Massimiliano FilostoDepartment of Clinical and Experimental Sciences, University of Brescia, ItalyCorreu electrònic verificat a unibs.it
Roberta MarozzoIRCCS San Camillo s.r.l.Correu electrònic verificat a ospedalesancamillo.net
Leonardo SalviatiProfessor of medical genetics, Dept. of Women and Children's Health, University of PadovaCorreu electrònic verificat a unipd.it
daniela tavianAssociate Professor of Biochemistry, Università Cattolica (Milano)Correu electrònic verificat a unicatt.it
Sara MissagliaUniversità Cattolica del Sacro CuoreCorreu electrònic verificat a unicatt.it
Giulio PilusoDip. di Medicina di Precisione, Università degli Studi della Campania "LuigiCorreu electrònic verificat a unicampania.it
Luciano MerliniIstituto Ortopedico Rizzoli, Bologna, ITCorreu electrònic verificat a unife.it

Segueix

Corrado Angelini

Professor of Neurology

Correu electrònic verificat a unipd.it

glycogenosis lipid storage myopathies carnitine muscular dystrophy


Títol Ordena per cites Ordena per any Ordena per títol	Citada per Citada per	Any
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	1104	1998
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	949	2012
Carnitine deficiency of human skeletal muscle with associated lipid storage myopathy: a new syndrome AG Engel, C Angelini Science 179 (4076), 899-902, 1973	680	1973
MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and … A Chomyn, A Martinuzzi, M Yoneda, A Daga, O Hurko, D Johns, ST Lai, ... Proceedings of the National Academy of Sciences 89 (10), 4221-4225, 1992	611	1992
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	610	1992
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	585	2017
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	546	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	527	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	498	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	354	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	329	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	317	1980
229th ENMC international workshop: Limb girdle muscular dystrophies–Nomenclature and reformed classification Naarden, the Netherlands, 17–19 March 2017 V Straub, A Murphy, B Udd, A Corrado, S Aymé, C Bönneman, ... Neuromuscular Disorders 28 (8), 702-710, 2018	309	2018
Correlating phenotype and genotype in the periodic paralyses TM Miller, MR Dias da Silva, HA Miller, H Kwiecinski, JR Mendell, R Tawil, ... Neurology 63 (9), 1647-1655, 2004	290	2004
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	279	1997
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	262	2000
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	258	1988
SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy E Pegoraro, EP Hoffman, L Piva, BF Gavassini, S Cagnin, M Ermani, ... Neurology 76 (3), 219-226, 2011	242	2011
The role of corticosteroids in muscular dystrophy: a critical appraisal C Angelini Muscle & Nerve: Official Journal of the American Association of …, 2007	241	2007
EFNS guidelines on the diagnostic approach to pauci‐or asymptomatic hyperCKemia T Kyriakides, C Angelini, J Schaefer, S Sacconi, G Siciliano, JJ Vilchez, ... European journal of neurology 17 (6), 767-773, 2010	240	2010

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