| A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo. A Simeone, D Acampora, A Mallamaci, A Stornaiuolo, MR D'Apice, ... The EMBO journal 12 (7), 2735-2747, 1993 | 699 | 1993 |
| Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene V Nigro, ES Moreira, G Piluso, M Vainzof, A Belsito, L Politano, AA Puca, ... Nature genetics 14 (2), 195-198, 1996 | 553 | 1996 |
| The human HOX gene family D Acampora, M D'Esposito, A Faiella, M Pannese, E Migliaccio, F Morelli, ... Nucleic acids research 17 (24), 10385-10402, 1989 | 393 | 1989 |
| Genetic basis of limb-girdle muscular dystrophies: the 2014 update V Nigro, M Savarese Acta Myologica 33 (1), 1, 2014 | 362 | 2014 |
| Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly S Brunelli, A Faiella, V Capra, V Nigro, A Simeone, A Cama, E Boncinelli Nature genetics 12 (1), 94-96, 1996 | 361 | 1996 |
| Differential regulation by retinoic acid of the homeobox genes of the four HOX loci in human embryonal carcinoma cells A Simeone, D Acampora, V Nigro, A Faiella, M D'Esposito, A Stornaiuolo, ... Mechanisms of development 33 (3), 215-227, 1991 | 361 | 1991 |
| 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 | 348 | 2018 |
| Identification of the Syrian hamster cardiomyopathy gene V Nigro, Y Okazaki, A Belsito, G Piluso, Y Matsuda, L Politano, G Nigro, ... Human molecular genetics 6 (4), 601-607, 1997 | 319 | 1997 |
| ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population E Benetti, R Tita, O Spiga, A Ciolfi, G Birolo, A Bruselles, G Doddato, ... European Journal of Human Genetics 28 (11), 1602-1614, 2020 | 279 | 2020 |
| Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophies L Politano, V Nigro, G Nigro, VR Petretta, L Passamano, S Papparella, ... Jama 275 (17), 1335-1338, 1996 | 266 | 1996 |
| Gentamicin administration in Duchenne patients with premature stop codon. Preliminary results. L Politano, G Nigro, V Nigro, G Piluso, S Papparella, O Paciello, LI Comi Acta Myologica: Myopathies and Cardiomyopathies: Official Journal of the …, 2003 | 258 | 2003 |
| The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies M Vainzof, MR Passos-Bueno, M Canovas, ES Moreira, RCM Pavanello, ... Human molecular genetics 5 (12), 1963-1969, 1996 | 232 | 1996 |
| Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein V Nigro, G Piluso, A Belsito, L Politano, AA Puca, S Papparella, E Rossi, ... Human molecular genetics 5 (8), 1179-1186, 1996 | 229 | 1996 |
| Orthopedia, a novel homeobox-containing gene expressed in the developing CNS of both mouse and Drosophila A Simeone, MR D'Apice, V Nigro, J Casanova, F Graziani, D Acampora, ... Neuron 13 (1), 83-101, 1994 | 211 | 1994 |
| Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contractures E Mercuri, K Bushby, E Ricci, D Birchall, M Pane, M Kinali, J Allsop, ... Neuromuscular Disorders 15 (2), 164-171, 2005 | 193 | 2005 |
| Evaluation of cardiac and respiratory involvement in sarcoglycanopathies L Politano, V Nigro, L Passamano, V Petretta, LI Comi, S Papparella, ... Neuromuscular disorders 11 (2), 178-185, 2001 | 186 | 2001 |
| Retinoic acid induces stage-specific antero-posterior transformation of rostral central nervous system A Simeone, V Avantaggiato, MC Moroni, F Mavilio, C Arra, F Cotelli, ... Mechanisms of development 51 (1), 83-98, 1995 | 173 | 1995 |
| γ1-and γ2-syntrophins, two novel dystrophin-binding proteins localized in neuronal cells G Piluso, M Mirabella, E Ricci, A Belsito, C Abbondanza, S Servidei, ... Journal of Biological Chemistry 275 (21), 15851-15860, 2000 | 168 | 2000 |
| Diagnostic value of muscle MRI in differentiating LGMD2I from other LGMDs D Fischer, MC Walter, K Kesper, JA Petersen, S Aurino, V Nigro, ... Journal of neurology 252, 538-547, 2005 | 165 | 2005 |
| Evaluation of the cardiomyopathy in Becker muscular dystrophy G Nigro, LI Comi, L Politano, FM Limongelli, V Nigro, ML De Rimini, ... Muscle & Nerve: Official Journal of the American Association of …, 1995 | 147 | 1995 |
Giulio PilusoDip. di Medicina di Precisione, Università degli Studi della Campania "LuigiGeverifieerd e-mailadres voor unicampania.it
