Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Hanna Björlin Avdic"'
Autor:
Charlotte Willfors, Jacqueline Borg, Johan Lundin Kleberg, Astrid Hallman, Marcus Van Der Poll, Karl Lundin Remnélius, Hanna Björlin Avdic, Sven Bölte, Ann Nordgren
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-12 (2024)
Abstract Williams syndrome (WS) is associated with atypical social communication and cognition reminiscent of the behaviours observed in autism. Nonetheless, WS also differs significantly from autism, such as regarding social motivation, which is typ
Externí odkaz:
https://doaj.org/article/f7701274778a49d6b4125a7340040fab
Autor:
Hanna Björlin Avdic, Claes Strannegård, Hedvig Engberg, Charlotte Willfors, Ida Nordgren, Louise Frisén, Angelica Lindén Hirschberg, Mona Guath, Ann Nordgren, Johan Lundin Kleberg
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract Turner syndrome is a genetic condition caused by a complete or partial loss of one of the X chromosomes. Previous studies indicate that Turner syndrome is associated with challenges in social skills, but the underlying mechanisms remain larg
Externí odkaz:
https://doaj.org/article/3a471176cc094b27a8ceb37afa52cfed
Autor:
Johan Lundin Kleberg, Charlotte Willfors, Hanna Björlin Avdic, Deborah Riby, Martyna A. Galazka, Mona Guath, Ann Nordgren, Claes Strannegård
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Williams syndrome (WS) is a rare genetic condition characterized by high social interest and approach motivation as well as intellectual disability and anxiety. Despite the fact that social stimuli are believed to have an increased intrinsic
Externí odkaz:
https://doaj.org/article/78f9795ba295482dababef0c7b2f4e75
Autor:
Hanna Björlin Avdic, Agnieszka Butwicka, Anna Nordenström, Catarina Almqvist, Agneta Nordenskjöld, Hedvig Engberg, Louise Frisén
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 13, Iss 1, Pp 1-9 (2021)
Abstract Background Turner syndrome is the result of the partial or complete absence of an X chromosome in phenotypic girls. This can cause an array of medical and developmental difficulties. The intelligence quotient in females with Turner syndrome
Externí odkaz:
https://doaj.org/article/405e4349ed4a461ca509a155cf522178
Autor:
Hanna Björlin Avdic, Johan Lundin Kleberg, Marcus van der Poll, Louise Frisén, Matilda Hutley, Mandi Sarjanen, Ida Nordgren, Katja Ekholm, Angelica Lindén Hirschberg, Ann Nordgren, Charlotte Willfors
Publikováno v:
Cognitive Neuropsychiatry. :1-19
Autor:
Johan Lundin Kleberg, Deborah Riby, Christine Fawcett, Hanna Björlin Avdic, Matilda A. Frick, Karin C. Brocki, Jens Högström, Eva Serlachius, Ann Nordgren, Charlotte Willfors
Williams syndrome (WS) is a rare genetic condition associated with high sociability, intellectual disability, and social cognitive challenges. Attention to others’ eyes is crucial for social understanding. Orienting to, and from other’s eyes was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c78cdbc35b3ab054032e55f06f42a1fd
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-490597
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-490597
Objective:Major depressive disorder (MDD) is associated with impaired reward processing and reward learning. The literature is inconclusive regarding whether these impairments persist after remission. The current study examined reward processing duri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba08d3a2ebef0b3cc4f09b10a02148a2
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-482608
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-482608
Autor:
Agneta Nordenskjöld, Agnieszka Butwicka, Hedvig Engberg, Louise Frisén, Catarina Almqvist, Anna Nordenström, Hanna Björlin Avdic
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 13, Iss 1, Pp 1-9 (2021)
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders
Background Turner syndrome is the result of the partial or complete absence of an X chromosome in phenotypic girls. This can cause an array of medical and developmental difficulties. The intelligence quotient in females with Turner syndrome has previ