Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Cecilia Henricson"'
Publikováno v:
Frontiers in Psychology, Vol 10 (2020)
Congenital cytomegalovirus (cCMV) infection is the most common cause of progressive hearing impairment. In our previous study around 90% of children with a cCMV infection and CI had severely damaged balance functions (Karltorp et al., 2014). Around 2
Externí odkaz:
https://doaj.org/article/42f24c2fe8184f37a2a8dc7a912702ea
Autor:
Filip Asp, Jeremy Wales, Eva Karltorp, Lena Anmyr, Britt-Marie Anderlid, Kristina Lagerstedt-Robinson, Henrik Smeds, Cecilia Henricson, Ulrika Löfkvist
Publikováno v:
Ear and Hearing
Supplemental Digital Content is available in the text.
Objective: Incomplete partition type 3 (IP3) malformation deafness is a rare hereditary cause of congenital or rapid progressive hearing loss. The children present with a severe to profound
Objective: Incomplete partition type 3 (IP3) malformation deafness is a rare hereditary cause of congenital or rapid progressive hearing loss. The children present with a severe to profound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aba7a2d6a3dd3f1ba7c4a8d202bb0aaa
http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-182207
http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-182207
Publikováno v:
Frontiers in Psychology
Congenital cytomegalovirus (cCMV) infection is the most common cause of progressive hearing impairment. In our previous study around 90% of children with a cCMV infection and CI had severely damaged balance functions (Karltorp et al., 2014). Around 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3f60b7246c8cab7d443e37f2d86d0f06
https://pubmed.ncbi.nlm.nih.gov/31998167
https://pubmed.ncbi.nlm.nih.gov/31998167
Publikováno v:
Journal of Visual Impairment & Blindness. 110:349-366
Objective Theory of mind (ToM) refers to the ability to impute mental states to one's self and others. ToM was investigated in adults with Usher syndrome type 2 (USH2) or Alström syndrome (AS). Both syndromes cause deafblindness, but differ with reg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e00ee7f01f109e60f6bb95307e7902f
https://doi.org/10.1177/0145482x1611000506
https://doi.org/10.1177/0145482x1611000506
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 76:1449-1457
Usher syndrome is a genetic condition causing deaf-blindness and is one of the most common causes of syndromic deafness. Individuals with USH1 in Sweden born during the last 15 years have typically received cochlear implants (CI) as treatment for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1772b3120dda978aba52e5d9cbe6c641
https://doi.org/10.1016/j.ijporl.2012.06.020
https://doi.org/10.1016/j.ijporl.2012.06.020
Autor:
Cecilia Henricson
Publikováno v:
Studies from the Swedish Institute for Disability Research ISBN: 9789176859995
Cognitive capacities and composite cognitive skills in individuals with Usher syndrome type 1 and 2
Cognitive capacities and composite cognitive skills in individuals with Usher syndrome type 1 and 2
The present thesis belongs to the research area disability research and deal with specific aspects of cognition in individuals with Usher syndrome type 1 and 2. The subject has been investigated an ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f78694b07e7554660a2866a4857f0e2
https://doi.org/10.3384/diss.diva-120114
https://doi.org/10.3384/diss.diva-120114
Autor:
Elina Mäki-Torkko, Cecilia Nakeva von Mentzer, Cecilia Henricson, Björn Lyxell, Inger Uhlén, Claes Möller, Lena Asker-Árnason, Tina Ibertsson, Birgitta Sahlén, Malin Wass
Hearing and cognitive development in deaf and hearing-impaired children : effects of intervention
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba983b25367ca26de462adf3360e7fcb
https://doi.org/10.1016/b978-0-7020-5310-8.00004-1
https://doi.org/10.1016/b978-0-7020-5310-8.00004-1