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V. Nigro

Nature Genetics, Mechanisms of Development, Neuromuscular Disorders, Acta myologica, Journal of the American Medical Association, European Journal of Human Genetics, Neuron, Human Molecular Genetics Show more
11
Role
Title
Level Year L/R
🦁 Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene
9 auth. V. Nigro, E. S. Moreira, G. Piluso, M. Vainzof, A. Belsito, L. Politano, ... A. Puca, M. Passos-Bueno, M. Zatz 		8 1996
8
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🐜 Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly
7 auth. S. Brunelli, A. Faiella, V. Capra, V. Nigro, A. Simeone, A. Cama, ... E. Boncinelli 		8 1996
8
🐜
🐜 Differential regulation by retinoic acid of the homeobox genes of the four HOX loci in human embryonal carcinoma cells
8 auth. A. Simeone, D. Acampora, V. Nigro, A. Faiella, M. D'Esposito, A. Stornaiuolo, ... F. Mavilio, E. Boncinelli 		8 1991
8
🐜
🐜 229th ENMC international workshop: Limb girdle muscular dystrophies – Nomenclature and reformed classification Naarden, the Netherlands, 17–19 March 2017
21 auth. V. Straub, A. Murphy, B. Udd, A. Corrado, S. Aymé, C. Bönneman, M. de Visser, A. Hamosh, Laura Jacobs, N. Khizanishvili, ... M. Kroneman, Pascal Laflorêt, A. Murphy, V. Nigro, L. Rufibach, A. Sarkozy, Shaun Swanepoel, Ivan Torrente, A. Urtizberea, J. Vissing, M. Walter 		8 2018
8
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🦁 Genetic basis of limb-girdle muscular dystrophies: the 2014 update
V. Nigro, M. Savarese 		7 2014
7
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🐜 Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophies.
8 auth. L. Politano, V. Nigro, G. Nigro, V. Petretta, L. Passamano, S. Papparella, ... S. Somma, Comi Li 		7 1996
7
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🐜 ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population
138 auth. E. Benetti, R. Tita, O. Spiga, A. Ciolfi, Giovanni Birolo, A. Bruselles, Gabriella Doddato, Annarita Giliberti, C. Marconi, F. Musacchia, T. Pippucci, A. Torella, A. Trezza, Floriana Valentino, M. Baldassarri, ... A. Brusco, R. Asselta, M. Bruttini, S. Furini, M. Seri, V. Nigro, G. Matullo, M. Tartaglia, F. Mari, E. Frullanti, C. Fallerini, Sergio Daga, Susanna Croci, S. Amitrano, F. Fava, F. Montagnani, Laura Di Sarno, A. Tommasi, Maria Palmieri, A. Emiliozzi, M. Fabbiani, B. Rossetti, G. Zanelli, L. Bergantini, M. D'alessandro, P. Cameli, D. Bennet, Federico Anedda, S. Marcantonio, S. Scolletta, F. Franchi, M. Mazzei, E. Conticini, L. Cantarini, B. Frediani, D. Tacconi, M. Feri, R. Scala, Genni Spargi, Marta Corridi, C. Nencioni, G. P. Caldarelli, Maurizio Spagnesi, P. Piacentini, M. Bandini, E. Desanctis, A. Canaccini, Chiara Spertilli, A. Donati, Luca Guidelli, L. Croci, A. Verzuri, Valentina Anemoli, A. Ognibene, M. Vaghi, A. d’Arminio Monforte, E. Merlini, M. Mondelli, S. Mantovani, S. Ludovisi, M. Girardis, S. Venturelli, M. Sita, A. Cossarizza, A. Antinori, A. Vergori, S. Rusconi, M. Siano, A. Gabrieli, A. Riva, D. Francisci, E. Schiaroli, P. Scotton, F. Andretta, S. Panese, R. Scaggiante, S. Parisi, F. Castelli, M. E. Quiros-Roldan, Paola Magro, C. Minardi, Deborah Castelli, Itala Polesini, M. Della Monica, C. Piscopo, M. Capasso, R. Russo, I. Andolfo, A. Iolascon, M. Carella, M. Castori, G. Merla, F. Aucella, P. Raggi, Carmen Marciano, Rita Perna, M. Bassetti, A. di Biagio, M. Sanguinetti, L. Masucci, C. Gabbi, S. Valente, S. Guerrini, I. Meloni, M. Mencarelli, C. L. Rizzo, E. Bargagli, M. Mandalà, A. Giorli, L. Salerni, G. Fiorentino, P. Zucchi, P. Parravicini, E. Menatti, S. Baratti, Tullio Trotta, Ferdinando Giannattasio, Gabriella Coiro, F. Lena, D. Coviello, C. Mussini, A. Renieri, A. Pinto 		7 2020
7
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🐜 Orthopedia, a novel homeobox-containing gene expressed in the developing CNS of both mouse and drosophila
7 auth. A. Simeone, M. D’Apice, V. Nigro, J. Casanova, F. Graziani, D. Acampora, ... V. Avantaggiato 		7 1994
7
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🐜 The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies.
12 auth. M. Vainzof, M. Passos-Bueno, M. Cánovas, E. Moreira, R. Pavanello, S. Marie, ... L. Anderson, C. Bönnemann, E. McNally, V. Nigro, L. Kunkel, M. Zatz 		7 1996
7
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🦁 Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene.
9 auth. V. Nigro, E. de Sá Moreira, G. Piluso, M. Vainzof, A. Belsito, L. Politano, ... A. Puca, M. Passos-Bueno, M. Zatz 		7 1996
7
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🐜 Retinoic acid induces stage-specific antero-posterior transformation of rostral central nervous system
8 auth. A. Simeone, V. Avantaggiato, M. Moroni, F. Mavilio, C. Arra, F. Cotelli, ... V. Nigro, D. Acampora 		7 1995
7
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