Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Maria Mallardi"'
Autor:
Domenico M. Romeo, Massimo Apicella, Giuseppina Leo, Maria Mallardi, Francesca Sini, Chiara Velli, Eugenio Mercuri
Publikováno v:
Heliyon, Vol 7, Iss 12, Pp e08648- (2021)
The emergency created by Coronavirus disease 2019 (COVID-19) has inevitably changed human normal social and relational habits. The use of personal protective equipment, like surgical masks, by healthcare workers has been recommended to prevent human-
Externí odkaz:
https://doaj.org/article/c3e7167148614d30831e6e2d541ffa10
Autor:
Domenico M. Romeo, Martina Ricci, Federica Mirra, Ilaria Venezia, Maria Mallardi, Elisa Pede, Eugenio Mercuri
Publikováno v:
Medicina, Vol 58, Iss 1, p 133 (2022)
Background and Objectives: Preterm infants are at higher risk of neurodevelopmental impairment both at preschool and school ages, even in the absence of major neurological deficits. The early identification of children at risk is essential for early
Externí odkaz:
https://doaj.org/article/2fd5f0d9e96a4d59b3ff998cc8090a7b
Autor:
Daniela Chieffo, Claudia Brogna, Angela Berardinelli, Grazia D'Angelo, Maria Mallardi, Adele D'Amico, Paolo Alfieri, Eugenio Mercuri, Marika Pane
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0133214 (2015)
ObjectiveNeurodevelopmental and cognitive difficulties are known to occur frequently in boys with Duchenne muscular dystrophy but so far none of the published studies have reported both early neurodevelopmental assessments and cognitive tests in the
Externí odkaz:
https://doaj.org/article/7d8e705c01714ece9c5011bb7a302689
Autor:
Eugenio Mercuri, Janette Atkinson, Valentina Laganà, Carolina Coppola, Serena Sivo, Daniela Ricci, Giorgia Coratti, Simona Lucibello, Domenico M. Romeo, Francesca Gallini, Mariaelisa Bartoli, Maria Mallardi, Francesca Tinelli, Oliver Braddick
Background The Early Childhood Attention Battery (ECAB) has been used to assess three different components of attention in preschool children, namely, selective, sustained and attentional control. Aim The aim of the study was: I) to adapt the ECAB to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98f5d721a8264f344d88805fbff9c35a
http://hdl.handle.net/10807/151773
http://hdl.handle.net/10807/151773
Autor:
Serena Sivo, Elisa Musto, Domenico M. Romeo, Emanuela Pagliano, Eugenio Mercuri, Daniela Ricci, Giovanni Baranello, Oliviero Bruni, Claudia Brogna, Tiziana Casalino, Domenica Battaglia, Maria Mallardi, Francesco Cota
Publikováno v:
Sleep Medicine. 15:1089-1093
Objectives The study aimed to analyze (i) the prevalence of sleep disorders in pre-school children with cerebral palsy (CP) using the Sleep Disturbance Scale for Children (SDSC), (ii) the possible association with motor, cognitive and behavioral prob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bb8bd35f5165f84bac661f70365a3bd
https://doi.org/10.1016/j.sleep.2014.05.008
https://doi.org/10.1016/j.sleep.2014.05.008
Autor:
Emanuela Pagliano, Annalisa Sacco, Tiziana Casalino, Serena Sivo, Elisa Musto, Daniela Ricci, Eugenio Mercuri, Domenico M. Romeo, Francesco Cota, Maria Mallardi, Michela Quintiliani, Giovanni Baranello, Domenica Battaglia, Claudia Brogna, Oliviero Bruni
Publikováno v:
Sleep Medicine. 15:213-218
We aimed to estimate the frequency of sleep disorders in children with cerebral palsy (CP) using the Sleep Disturbance Scale for Children (SDSC) and to evaluate the relations between sleep disorders and motor, cognitive, and behavioral problems.One h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::746fa4c3a339d58cacbf05b1eb0e34eb
https://doi.org/10.1016/j.sleep.2013.08.793
https://doi.org/10.1016/j.sleep.2013.08.793
Autor:
Maria Mallardi, Marco Tartaglia, Maria Cristina Digilio, Stefano Vicari, Cristina Caciolo, Eugenio Mercuri, Giorgia Piccini, Chiara Leoni, Maria Luigia Gambardella, Francesca Pantaleoni, Nadia Mirante, Paolo Alfieri, Laura Cesarini, Giuseppe Zampino
Publikováno v:
Behavior Genetics. 41:423-429
In the present study we evaluated long term memory in twenty individuals with molecularly confirmed diagnosis of Noonan syndrome and LEOPARD syndrome, two disorders caused by mutations in genes coding transducers participating in the RAS-MAPK signali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f3804d57b2a67b699293fb194514ae0
https://doi.org/10.1007/s10519-011-9446-5
https://doi.org/10.1007/s10519-011-9446-5
Autor:
Janette Atkinson, Fleur Corbett, Christine Montague-Johnson, Maria Mallardi, Paola Mattei, Daniela Ricci, Jessica Galli, Giorgia Coratti, Oliver Braddick, Elisa Fazzi, Jeremy R. Parr, Serena Micheletti, Morag Andrew, Peter B. Sullivan
Publikováno v:
Journal of Vision. 18:546
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8eb278e525078a0d4c62602faca4c2a
https://doi.org/10.1167/18.10.546
https://doi.org/10.1167/18.10.546
Autor:
Eugenio Mercuri, Adele D'Amico, Grazia D'Angelo, Maria Mallardi, Claudia Brogna, Daniela Chieffo, Marika Pane, Angela Berardinelli, Paolo Alfieri
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 8, p e0133214 (2015)
PLoS ONE, Vol 10, Iss 8, p e0133214 (2015)
ObjectiveNeurodevelopmental and cognitive difficulties are known to occur frequently in boys with Duchenne muscular dystrophy but so far none of the published studies have reported both early neurodevelopmental assessments and cognitive tests in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00ae7ebbc23feb7cbc63ddd795f6b138
https://pubmed.ncbi.nlm.nih.gov/26275215
https://pubmed.ncbi.nlm.nih.gov/26275215
Autor:
Paolo Alfieri, Maria Luigia Gambardella, Chiara Fossati, Cristina Caciolo, Angelo Selicorni, Maria Cristina Digilio, Giuseppe Zampino, Daniela Leone, Stefano Vicari, Laura Cesarini, Chiara Leoni, Marco Tartaglia, Eugenio Mercuri, Francesca Perrino, Giorgia Piccini, Maria Mallardi
Publikováno v:
American journal of medical genetics. Part A. (4)
Here, we describe neurobehavioral features in patients with RASopathies (i.e., Noonan syndrome, LEOPARD syndrome, Costello syndrome, and cardiofaciocutaneous syndrome), developmental disorders caused by mutations in genes coding transducers participa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::032b108b0b08b1a19196514ca42657e7
https://pubmed.ncbi.nlm.nih.gov/24458522
https://pubmed.ncbi.nlm.nih.gov/24458522