Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Liv Øinæs Andersen"'
Publikováno v:
PLoS ONE, Vol 13, Iss 12, p e0207846 (2018)
ObjectivesTo describe level of education and work participation among adults with congenital unilateral upper limb deficiency (CUULD) in Norway and to explore associations between work participation and demographic and clinical factors.MethodsCross-s
Externí odkaz:
https://doaj.org/article/383e6adfc73f460fa7114f40ecba895a
Publikováno v:
PLoS ONE, Vol 13, Iss 1, p e0190567 (2018)
To describe Norwegian adults with congenital unilateral upper limb deficiency (CUULD) regarding self-reported chronic pain (intensity, locations, impact on daily life) and fatigue. Analyze associations between chronic pain and demographic/clinical fa
Externí odkaz:
https://doaj.org/article/c2a79a4917e14be9ae152f205082147c
Publikováno v:
Disability and Rehabilitation. 38:2305-2314
To examine subjective health-related quality of life (HRQoL) in adults with congenital unilateral upper limb deficiency (UULD) in Norway and to explore the associations between demographic and clinical factors and HRQoL.Cross-sectional study comparin
Publikováno v:
Disability and Rehabilitation. 38:1803-1810
To describe clinical features, issues related to school life and health-related quality of life (HRQOL) for children with congenital limb deficiency (CLD) and compare these children to Norwegian school children on HRQOL.Cross-sectional study. In 2010
Publikováno v:
PLoS ONE
PLoS ONE, Vol 13, Iss 12, p e0207846 (2018)
PLoS ONE, Vol 13, Iss 12, p e0207846 (2018)
ObjectivesTo describe level of education and work participation among adults with congenital unilateral upper limb deficiency (CUULD) in Norway and to explore associations between work participation and demographic and clinical factors.MethodsCross-s
Publikováno v:
Disability and Rehabilitation. 37:2076-2082
To describe an adult population with congenital limb deficiency (CLD) recruited through the National Resource Centre for Rare Disorders (TRS) in Norway: (1) demographic factors, (2) clinical features, (3) pain and (4) use of health care and welfare s
Autor:
Trine Bathen, Anett Bjørnødegård Hångmann, Liv Øinæs Andersen, Svend Rand-Hendriksen, Marie Hoff
Publikováno v:
American journal of medical genetics. Part A. (12)
Ehlers-Danlos Syndrome hypermobility type (EDS-HT) and joint hypermobility syndrome (JHS) are two overlapping heritable connective tissue disorders. Patients with these conditions have many and various complaints; limitations in performing daily acti