Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Luciana Losito"'
Autor:
Luisa Santangelo, Giuseppe Stefano Netti, Diletta Domenica Torres, Giovanni Piscopo, Vincenza Carbone, Luciana Losito, Leonardo Milella, Maria Luigia Lasorella, Pasquale Conti, Delio Gagliardi, Maria Chironna, Federica Spadaccino, Elena Bresin, Antonio Trabacca, Elena Ranieri, Mario Giordano
Publikováno v:
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-8 (2021)
Abstract Background The Neurological involvement is the most common extra-renal complication of Shiga toxin-producing E. coli-hemolytic uremic syndrome (HUS) or typical HUS. On brain magnetic resonance examination, main neurological signs encompass a
Externí odkaz:
https://doaj.org/article/730ffbe2a17a4d56ba88e2904bdb57a1
Autor:
Marta Simone, Antonio Trabacca, Elena Panzeri, Luciana Losito, Andrea Citterio, Maria Teresa Bassi
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
This paper describes the clinical evolution and the novel genetic findings in a KIF5A mutated family previously reported as affected by spastic paraparesis only. The additional evidence we report here, a homozygous ALS2 mutation detected in the proba
Externí odkaz:
https://doaj.org/article/deabacf8ffec42168cdc87c87d49e9f7
Publikováno v:
Acta Neurologica Belgica. 121:1883-1885
Autor:
Francesco Nicita, Elena Panzeri, Cristina Maghini, Fabrizia Stregapede, Antonio Pizzuti, Maria Teresa Bassi, Guja Astrea, Piotr Gasperowicz, Melissa Barghigiani, Guido Primiano, Enrico Bertini, Ginevra Zanni, Marta Nardella, Aleksandra Jezela-Stanek, Luciana Losito, Rafał Płoski, Alessandra Tessa, Lorena Travaglini, Serenella Servidei, Filippo M. Santorelli
Publikováno v:
Journal of Neurology. 266:2657-2664
Recessive mutations in DDHD2 cause SPG54, a complex hereditary spastic paraplegia (HSP) with less than forty patients reported worldwide. In this retrospective, multicenter study we describe eight additional SPG54 cases harboring homozygous or compou
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 42(9)
Autor:
Elena Bresin, Antonio Trabacca, Vincenza Carbone, Diletta Domenica Torres, Giuseppe Stefano Netti, Leonardo Milella, Delio Gagliardi, Giovanni Piscopo, Elena Ranieri, Mario Giordano, Luisa Santangelo, Luciana Losito, Maria Luigia Lasorella, Maria Chironna, Pasquale Conti
Background. The Neurological involvement is the most common extra-renal complication of Shiga toxin-producing Escherichia coli-hemolytic uremic syndrome (STEC-HUS). On brain magnetic resonance examination, main neurological signs encompass acute lesi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::892c1d7a78c73e87634299c73a3efce6
https://doi.org/10.21203/rs.3.rs-242540/v1
https://doi.org/10.21203/rs.3.rs-242540/v1
Autor:
Diletta Domenica Torres, Maria Luigia Lasorella, Maria Chironna, Giuseppe Stefano Netti, Mario Giordano, Elena Ranieri, Luisa Santangelo, Delio Gagliardi, Giovanni Piscopo, Leonardo Milella, Vincenza Carbone, Pasquale Conti, Luciana Losito, Federica Spadaccino, Antonio Trabacca, Elena Bresin
Publikováno v:
Italian Journal of Pediatrics
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-8 (2021)
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-8 (2021)
Background The Neurological involvement is the most common extra-renal complication of Shiga toxin-producing E. coli-hemolytic uremic syndrome (HUS) or typical HUS. On brain magnetic resonance examination, main neurological signs encompass acute lesi
Autor:
Antonella Di Liddo, Rossella Pacifico, Antonio Trabacca, Luciana Losito, Teresa Vespino, Elisabetta Lucarelli
Publikováno v:
European journal of physical and rehabilitation medicine. 56(2)
Background Management of spinal muscular atrophy (SMA) has progressed enormously and reached unprecedented levels with nusinersen gene therapy. We are finally able to counter the progression of this devastating genetic disease, contributing to the de
Autor:
Andrea Citterio, Elena Panzeri, Marta Simone, Antonio Trabacca, Maria Teresa Bassi, Luciana Losito
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
Frontiers in Neurology
Frontiers in Neurology
This paper describes the clinical evolution and the novel genetic findings in a KIF5A mutated family previously reported as affected by spastic paraparesis only. The additional evidence we report here, a homozygous ALS2 mutation detected in the proba
Autor:
Serena Camposeo, Antonio Trabacca, Luciana Losito, Jlenia Maniglio, Teresa Vespino, Leonarda Gennaro, Marta De Rinaldis, Eliana Compagnone
Publikováno v:
Research in Developmental Disabilities. 35:2651-2657
This study aimed to investigate a possible correlation between the gross motor function classification system-expanded and revised (GMFCS-ER), the manual abilities classification system (MACS) and the communication function classification system (CFC