Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Laura Malerba"'
Autor:
Jessica Galli, Erika Loi, Lucrezia Maria Visconti, Paola Mattei, Anna Eusebi, Stefano Calza, Elisa Fazzi, ASD Collaborative Group, Luisa Bonini, Angela Merlini, Laura Pansera, Laura Malerba, Filippo Gitti
Publikováno v:
Frontiers in Psychiatry, Vol 13 (2022)
BackgroundSleep disturbances are common in children affected by Autism Spectrum Disorder (ASD). The aim of our study was to describe sleep characteristics and disturbances in children with ASD, to evaluate possible related factors, and to assess pare
Externí odkaz:
https://doaj.org/article/68d340a4529a4c76b719bdb80fe2f6a9
Autor:
Marco Zecca, Barbara Gardella, Elena Grossi, Roberto Giorda, Elisa Fazzi, Simona Orcesi, Anna Cavallini, Livio Provenzi, Renato Borgatti, Pierangelo Veggiotti, Serena Grumi, Giacomo Biasucci, Renza Bonini, Lidia Decembrino, Bruno Drera, Rossana Falcone, Roberta Giacchero, Renata Nacinovich, Camilla Pisoni, Federico Prefumo, Barbara Scelsa, Maria Valentina Spartà, Patrizia Accorsi, Rossana Bucci, Elisa Cavalleri, Laura Malerba, Paola Martelli, Mario Motta, Sonia Zatti, Emanuela Bertazzoli, Giovanna Centinaio, Maria Roberta Longo, Benedetta Chiara Pietra, Caterina Sabatini, Alberto Chiara, Giuliana Del Campo, Luisa Magnani, Dario Pantaleo, Arsenio Spinillo, Giulia Bensi, Cristiana Pavesi, Daniela Russo, Gaia Kullmann
Publikováno v:
BMJ Open, Vol 10, Iss 12 (2020)
Introduction COVID-19 is a highly infectious respiratory disease that rapidly emerged as an unprecedented epidemic in Europe, with a primary hotspot in Northern Italy during the first months of 2020. Its high infection rate and rapid spread contribut
Externí odkaz:
https://doaj.org/article/140886049d5a49c88b0ffb8705d7f57d
Publikováno v:
American Journal of Medical Genetics Part A.
Autor:
Giacomo Lus, Marco André Bassano, Vincenzo Brescia Morra, Simona Bonavita, Antonio Gallo, Davide Maimone, Laura Malerba, Giorgia Teresa Maniscalco, Francesco Saccà, Giuseppe Salemi, Renato Turrini, Salvatore Cottone, Edoardo Sessa, Maria Buccafusca, Luigi Maria Edoardo Grimaldi
Objective Multiple sclerosis (MS) is a chronic disease with different clinical courses and a tendency to worsening. The relapsing–remitting MS presents acute onset and relapses of neurological symptoms, followed by their remission. This form can co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50371d25c7838ee1d02013753799b373
https://hdl.handle.net/10447/584673
https://hdl.handle.net/10447/584673
Autor:
Renzo Guerrini, Lucio Giordano, Elena Parrini, Ilaria Bestetti, Laura Malerba, Sara Brunetti, Cecilia Parazzini, Giovanni Palumbo, Patrizia Accorsi
Publikováno v:
American Journal of Medical Genetics Part A. 185:2526-2531
Cerebral folate transporter deficiency syndrome, caused by FOLR-1 mutations is characterized by late infantile onset, severe developmental regression, epilepsy, and leukodystrophy. An extremely low concentration of 5-methyltetrahydrofolate in the cer
Autor:
Jessica Galli, Erika Loi, Lucrezia Maria Visconti, Paola Mattei, Anna Eusebi, Stefano Calza, Elisa Fazzi, ASD Collaborative Group, Luisa Bonini, Angela Merlini, Laura Pansera, Laura Malerba, Filippo Gitti
Publikováno v:
Frontiers in Psychiatry, Vol 13 (2022)
BackgroundSleep disturbances are common in children affected by Autism Spectrum Disorder (ASD). The aim of our study was to describe sleep characteristics and disturbances in children with ASD, to evaluate possible related factors, and to assess pare
Publikováno v:
Neuropediatrics. 49:S1-S12
Autor:
Andrea, Rossi, Marco, Gnesi, Cristina, Montomoli, Gaetano, Chirico, Laura, Malerba, Merabet, Lotfi B., NAVEG Study Group, Alessandrini, A, D’Adda, N, Tansini, F, Micheletti, S, Galli, J, Accorsi, P, Martelli, P, Gritti, M, Mattei, P, Bettelli, S, Franzoni, A, Nascimbeni, G, Semeraro, F, Gasparoni, A, Ferrari, F, Della Casa, E, Orcesi, S, Stronati, M, Lebrun, F, Marcou, V, Haumont, D, Tackoen, M, Fazzi, ELISA MARIA
Publikováno v:
Infant Behavior and Development. 49:21-30
Purpose Children with Childhood Absence Epilepsy (CAE) may develop generalized tonic-clonic seizure or juvenile myoclonic epilepsy. A possible evolution to Eyelid Myoclonia with Absence Epilepsy (EMA) hasn’t been documented yet. We report the elect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6435fa0ca62053aaf8a66dad97147f8a
http://hdl.handle.net/11379/511174
http://hdl.handle.net/11379/511174