Zobrazeno 1 - 10
of 10
pro vyhledávání: '"María Novelli"'
Publikováno v:
Cadernos de Gênero e Diversidade, Vol 2, Iss 1 (2016)
Anahi Guedes de Mello es una de las más importantes teóricas emergentes de la discapacidad en Brasil. Antropóloga de formación, es diplomada y licenciada en Ciencias Sociales, con maestría en Antropología Social por la Universidad Federal de Sa
Externí odkaz:
https://doaj.org/article/16124b8e0dae4fb3a23c322a766190bd
Autor:
Maria Novelli, Elvira Caramuscio, Fabio Natale, Cristina Zitarelli, Rosa Ferri, Gianluca Terrin, Barbara Caravale
Publikováno v:
Global Pediatrics, Vol 9, Iss , Pp 100192- (2024)
Introduction: Infants with congenital CMV (cCMV) infection may show manifestations at birth and develop symptomatic disease, although the majority have no apparent clinical signs and should be considered asymptomatic (acCMV). Studies about neurodevel
Externí odkaz:
https://doaj.org/article/919d70e76417422e9285286a9f65debd
Autor:
Maria Novelli, Valeria Mammarella, Francesca Calandriello, Sara Temofonte, Marina Goldoni, Ilaria Macchiarulo, Paolo Versacci, Antonio Pizzuti, Jessica Petrilli, Carlo Di Brina, Barbara Caravale
Publikováno v:
Global Pediatrics, Vol 9, Iss , Pp 100179- (2024)
Objective: UPD(16)mat is a rare genetic condition characterized by intrauterine growth deficiency and multiple congenital malformations. To the best of our knowledge, neurodevelopmental disorders have never been described in association with UPD(16)m
Externí odkaz:
https://doaj.org/article/f47c47c4352a428688d23e8224e897d7
Autor:
Maria Novelli, Fabio Natale, Anna Di Norcia, Arianna Boiani, Sara Temofonte, Francesca Calandriello, Cristina Zitarelli, Barbara Caravale
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-7 (2022)
Abstract Background Approximately 85–90% of congenital cytomegalovirus infections (cCMV) are asymptomatic. Few studies have investigated early and long-term neurodevelopmental outcomes in children with asymptomatic cCMV (acCMV), and the data is con
Externí odkaz:
https://doaj.org/article/eab5ee8da61449a598dbaa8613641730
Autor:
Giulia Conte, Carola Costanza, Maria Novelli, Veronica Scarselli, Elena Arigliani, Francesca Valente, Valentina Baglioni, Arianna Terrinoni, Flavia Chiarotti, Francesco Cardona
Publikováno v:
Children, Vol 11, Iss 2, p 226 (2024)
Background: Cognitive functions represent foundational factors for mental health and quality of life (QoL). In Tourette syndrome (TS), psychiatric comorbidities are common and have been inconsistently reported to affect the cognition and QoL of patie
Externí odkaz:
https://doaj.org/article/029dc212e1464bb39a747c6f58c90362
Publikováno v:
Cadernos de Gênero e Diversidade, Vol 2, Iss 1 (2016)
Anahi Guedes de Mello es una de las más importantes teóricas emergentes de la discapacidad en Brasil. Antropóloga de formación, es diplomada y licenciada en Ciencias Sociales, con maestría en Antropología Social por la Universidad Federal de Sa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd06b15f446b775d137482ed9a37edbe
https://doi.org/10.9771/cgd.v2i1.20437
https://doi.org/10.9771/cgd.v2i1.20437
Publikováno v:
Medicina (Buenos Aires), Vol 64, Iss 6, Pp 525-528 (2004)
Se presenta el caso infrecuente de un paciente con miopatía visceral esporádica y afectación de la totalidad del tracto gastrointestinal y de la vía urinaria. La miopatía visceral es una forma de pseudo-obstrucción intestinal crónica idiopáti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::a549f18c1fb890b888ce92f410e734ca
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0025-76802004000600009
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0025-76802004000600009
Autor:
Serena Galosi, Luca Pollini, Maria Novelli, Katerina Bernardi, Martina Di Rocco, Simone Martinelli, Vincenzo Leuzzi
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Over the last years, a constantly increasing number of genetic diseases associated with epilepsy and movement disorders have been recognized. An emerging group of conditions in this field is represented by genetic disorders affecting G-protein-couple
Externí odkaz:
https://doaj.org/article/2f6781d6cdeb48f689b72d476437e346
Autor:
Pedro, Montalvo, Liliana, Paz, Elsa, Chiappa, Sandra, Aronne, María, Novelli, María Elena, Biaiñ
Publikováno v:
Medicina. 64(6)
We report an unusual case of a patient with sporadic visceral myopathy and involvement of the entire gastrointestinal and urinary tract. Visceral myopathy is a form of chronic idiophatic intestinal pseudo-obstruction characterized by vacuolar degener
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::31f01d2f6301018eca3f560adab1c575
https://pubmed.ncbi.nlm.nih.gov/15637831
https://pubmed.ncbi.nlm.nih.gov/15637831
Autor:
Veronica Scarselli, Melania Martucci, Maria Novelli, Serena Galosi, Maria Romani, Carla Sogos
Publikováno v:
Behavioral Sciences, Vol 12, Iss 10, p 382 (2022)
Autism Spectrum Disorder (ASD) and attention deficit hyperactivity disorder (ADHD) comorbidity is common in clinical practice and it seems to be related to shared etiological mechanisms and genetic susceptibility. Moreover, occurrence of psychosis ca
Externí odkaz:
https://doaj.org/article/6a0a05b0402d463e85707f827175f896