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1دورية أكاديمية
المؤلفون: Nicita, Francesco, Ginevrino, Monia, Travaglini, Lorena, D'Arrigo, Stefano, Zorzi, Giovanna, Borgatti, Renato, Terrone, Gaetano, Catteruccia, Michela, Vasco, Gessica, Brankovic, Vesna, Siliquini, Sabrina, Romano, Silvia, Veredice, Chiara, Pedemonte, Marina, Armando, Michelina, Lettori, Donatella, Stregapede, Fabrizia, Bosco, Luca, Sferra, Antonella, Tessarollo, Valeria, Romaniello, Romina, Ristori, Giovanni, Bertini, Enrico, Valente, Enza Maria, Zanni, Ginevra
المساهمون: H2020 European Research Council, Italian Ministry of Health, Fondazione Pierfranco e Luisa Mariani
المصدر: Journal of Medical Genetics ; volume 58, issue 7, page 475-483 ; ISSN 0022-2593 1468-6244
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2دورية أكاديمية
المؤلفون: Nicita, Francesco, Ginevrino, Monia, Travaglini, Lorena, D'Arrigo, Stefano, Zorzi, Giovanna, Borgatti, Renato, Terrone, Gaetano, Catteruccia, Michela, Vasco, Gessica, Brankovic, Vesna, Siliquini, Sabrina, Romano, Silvia, Veredice, Chiara, Pedemonte, Marina, Armando, Michelina, Lettori, Donatella, Stregapede, Fabrizia, Bosco, Luca, Sferra, Antonella, Tessarollo, Valeria
المصدر: Journal of Medical Genetics; Jul2021, Vol. 58 Issue 7, p475-483, 9p
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3دورية أكاديمية
المؤلفون: NICITA, Francesco, BERTINI, Enrico, TRAVAGLINI, LORENA, Armando, Michelina, Aiello, Chiara
المساهمون: Nicita, Francesco, Bertini, Enrico, Travaglini, Lorena, Armando, Michelina, Aiello, Chiara
مصطلحات موضوعية: H-ABC, Hereditary spastic paraplegia, Hypomyelination, Leukodystrophy, TUBB4A, Neurology, Neurology (clinical)
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/27538619; info:eu-repo/semantics/altIdentifier/wos/WOS:000382415700028; volume:368; firstpage:145; lastpage:146; numberofpages:2; journal:JOURNAL OF THE NEUROLOGICAL SCIENCES; http://hdl.handle.net/11573/930448Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84977642195; www.elsevier.com/locate/jns
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4دورية
المؤلفون: Nicita, Francesco, Ginevrino, Monia, Travaglini, Lorena, D'Arrigo, Stefano, Zorzi, Giovanna, Borgatti, Renato, Terrone, Gaetano, Catteruccia, Michela, Vasco, Gessica, Brankovic, Vesna, Siliquini, Sabrina, Romano, Silvia, Veredice, Chiara, Pedemonte, Marina, Armando, Michelina, Lettori, Donatella, Stregapede, Fabrizia, Bosco, Luca, Sferra, Antonella, Tessarollo, Valeria, Romaniello, Romina, Ristori, Giovanni, Bertini, Enrico, Valente, Enza Maria, Zanni, Ginevra
المصدر: Journal of Medical Genetics (JMG); 2021, Vol. 58 Issue: 7 p475-483, 9p
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5دورية أكاديمية
المؤلفون: Petrarca, Maurizio, Cappa, Paolo, Zanelli, Giulia, Armando, Michelina, Castelli, Enrico, Berthoz, Alain
المساهمون: Italian Ministry of University, Italian Health Ministry, Italian-French University
المصدر: Gait & Posture ; volume 37, issue 4, page 494-499 ; ISSN 0966-6362
مصطلحات موضوعية: Rehabilitation, Orthopedics and Sports Medicine, Biophysics
الإتاحة: https://doi.org/10.1016/j.gaitpost.2012.08.022Test
https://api.elsevier.com/content/article/PII:S096663621200327X?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S096663621200327X?httpAccept=text/plainTest -
6دورية أكاديمية
المؤلفون: Francesco Nicita, Monia Ginevrino, Lorena Travaglini, Stefano D'Arrigo, Giovanna Zorzi, Renato Borgatti, Gaetano Terrone, Michela Catteruccia, Gessica Vasco, Vesna Brankovic, Sabrina Siliquini, Silvia Romano, Chiara Veredice, Marina Pedemonte, Michelina Armando, Donatella Lettori, Fabrizia Stregapede, Luca Bosco, Antonella Sferra, Valeria Tessarollo, Romina Romaniello, Giovanni Ristori, Enrico Bertini, Enza Maria Valente, Ginevra Zanni
المساهمون: Nicita, Francesco, Ginevrino, Monia, Travaglini, Lorena, D'Arrigo, Stefano, Zorzi, Giovanna, Borgatti, Renato, Terrone, Gaetano, Catteruccia, Michela, Vasco, Gessica, Brankovic, Vesna, Siliquini, Sabrina, Romano, Silvia, Veredice, Chiara, Pedemonte, Marina, Armando, Michelina, Lettori, Donatella, Stregapede, Fabrizia, Bosco, Luca, Sferra, Antonella, Tessarollo, Valeria, Romaniello, Romina, Ristori, Giovanni, Bertini, Enrico, Valente, ENZA MARIA, Zanni, Ginevra
مصطلحات موضوعية: central nervous system disease, cerebellar disease, genetic heterogeneity, neurodegenerative disease, neurology
العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000680409100005; volume:58; issue:7; firstpage:475; lastpage:483; numberofpages:9; journal:JOURNAL OF MEDICAL GENETICS; http://hdl.handle.net/11588/815017Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85093677649
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7
المؤلفون: Michela Catteruccia, Francesco Nicita, Enrico Bertini, Fabrizia Stregapede, Stefano D'Arrigo, Monia Ginevrino, Renato Borgatti, Silvia Romano, Giovanna Zorzi, V. Brankovic, Ginevra Zanni, Romina Romaniello, Lorena Travaglini, Luca Bosco, Giovanni Ristori, Sabrina Siliquini, Gessica Vasco, Valeria Tessarollo, Marina Pedemonte, C. Veredice, Gaetano Terrone, Donatella Lettori, M. Armando, Antonella Sferra, Enza Maria Valente
المساهمون: Nicita, Francesco, Ginevrino, Monia, Travaglini, Lorena, D'Arrigo, Stefano, Zorzi, Giovanna, Borgatti, Renato, Terrone, Gaetano, Catteruccia, Michela, Vasco, Gessica, Brankovic, Vesna, Siliquini, Sabrina, Romano, Silvia, Veredice, Chiara, Pedemonte, Marina, Armando, Michelina, Lettori, Donatella, Stregapede, Fabrizia, Bosco, Luca, Sferra, Antonella, Tessarollo, Valeria, Romaniello, Romina, Ristori, Giovanni, Bertini, Enrico, Valente, ENZA MARIA, Zanni, Ginevra
مصطلحات موضوعية: medicine.medical_specialty, Ataxia, Neurology, central nervous system disease, cerebellar diseases, Central nervous system diseases, genetic heterogeneity, neurodegenerative diseases, neurology, Bioinformatics, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, neurodegenerative disease, Hereditary sensory and autonomic neuropathy, Genetics, Medicine, Missense mutation, Genetics (clinical), 030304 developmental biology, KIF1A, 0303 health sciences, business.industry, Genetic heterogeneity, cerebellar disease, medicine.disease, 3. Good health, Peripheral neuropathy, medicine.symptom, business, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cac658580084597d826ecd2ee68cf8e3Test
http://hdl.handle.net/11573/1473001Test