Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Virginia, Canegallo"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-14 (2022)
Abstract Background Rett Syndrome (RTT) is a severe, neurodevelopmental disorder mainly caused by mutations in the MECP2 gene, affecting around 1 in 10,000 female births. Severe physical, language, and social impairments impose a wide range of limita
Externí odkaz:
https://doaj.org/article/7f0cd25ef0874d6fbd179a1ac92d5953
Publikováno v:
Current Developmental Disorders Reports. 10:1-13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e1f9326ddd9ba7113384c99a50bd57d
https://doi.org/10.1007/s40474-023-00269-5
https://doi.org/10.1007/s40474-023-00269-5
Background: Rett Syndrome (RTT) is a severe, neurodevelopmental disorder mainly caused by mutations in the MECP2 gene, affecting around 1 in 10,000 female births. Severe physical, language, and social impairments impose a wide range of limitations in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::159806483839e3a007aada834a92be33
https://doi.org/10.21203/rs.3.rs-1627288/v1
https://doi.org/10.21203/rs.3.rs-1627288/v1
Autor:
Giancarlo Iannizzotto, Samantha Giannatiempo, Tindara Caprì, Virginia Canegallo, Martina Semino, Alberto Romano, Rosa Angela Fabio, Fabrizio Stasolla, Andrea Nucita
We conducted a systematic review of telerehabilitation (TR) interventions on children and young adults with multiple disabilities (MDs). This review aimed to (a) examine the effectiveness of telerehabilitation (TR) on adaptive skills that have been t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bc28344c4c8283661a625c0aa314544
http://hdl.handle.net/10807/177524
http://hdl.handle.net/10807/177524