Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Nina Strømsvik"'
Autor:
Nina Strømsvik, Pernilla Olsson, Berit Gravdehaug, Hilde Lurås, Ellen Schlichting, Kjersti Jørgensen, Teresia Wangensteen, Tone Vamre, Cecilie Heramb, Lovise Mæhle, Eli Marie Grindedal
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 20, Iss 1, Pp 1-11 (2022)
Abstract Background In South-Eastern Norway, genetic testing for BRCA1 and BRCA2 is offered to breast cancer patients by their treating surgeon or oncologist. Genetic counselling from a geneticist or a genetic counsellor is offered only to those who
Externí odkaz:
https://doaj.org/article/7405b384fb0e4506be52a64cf8bd99d2
Publikováno v:
Journal of Genetic Counseling
Recontacting former patients regarding new genetic information is currently not standard care but might be implemented in the future. Little information is available on the implications of this practice from the point of view of former patients. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81e7b09a8f38b3e7ac08a1de24bf31ae
https://hdl.handle.net/11250/2827549
https://hdl.handle.net/11250/2827549
Autor:
Jill Walker Rettberg, Thomas Akselberg Hatlebrekke, Elen Siglen, Anniken Hamang, Aslaug Beathe Forberg Lunde, Nina Strømsvik, Vidar M. Steen, Sigrid Tronsli Hovland, Hildegunn Høberg Vetti, Cathrine Bjorvatn
Publikováno v:
Patient Education and Counseling
Objective: We aimed at developing a pilot version of an app (Rosa) that can perform digital conversations with breast or ovarian cancer patients about genetic BRCA testing, using chatbot technology, to identify best practices for future patient-focus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::925b81d7e030272786186b078c0e0a21
https://hdl.handle.net/11250/2838901
https://hdl.handle.net/11250/2838901
Autor:
Christoffer Jonsrud, Geir Åsmund Myge Hansen, Marijke Van Ghelue, Hilde Monica Frostad Riise Stensland, Siri Skarsfjord, Nina Strømsvik, Elisabeth Jarhelle, Monica Ingebrigtsen
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-12 (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-12 (2019)
Families with breast and ovarian cancer are often tested for disease associated sequence variants in BRCA1 and BRCA2. Pathogenic sequence variants (PVs) in these two genes are known to increase breast and ovarian cancer risks in females. However, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8c32e64986e163086a2e4c84ca7b494
https://hdl.handle.net/10037/17238
https://hdl.handle.net/10037/17238
Publikováno v:
Journal of Genetic Counseling
Women identified as BRCA1 and BRCA2 mutation carriers are advised to manage their cancer risk through intensive screening programs and/or by undergoing risk-reducing surgery. The aim of this study was to explore and describe the experiences of female
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e29eb8004632417d91077bcc67f79f3
https://doi.org/10.1007/s10897-016-9954-9
https://doi.org/10.1007/s10897-016-9954-9
Publikováno v:
Nursing children and young people. 30(2)
Aim To explore the collaboration challenges faced by neonatal intensive care unit (NICU) nurses and public health nurses when preparing premature infants for transition home and to explore the culture of cooperation between the two professional group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc21921aec397196ce940dfd9158f741
https://pubmed.ncbi.nlm.nih.gov/29512964
https://pubmed.ncbi.nlm.nih.gov/29512964
Publikováno v:
Familial Cancer
This qualitative study explored the experiences of Norwegian men after being identified as BRCA 1/2 mutation-positive. Only limited knowledge is available on this topic; therefore, the aim of this study was to gain a deeper insight from the men’s o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::377b76cf12ead715ea6b17ca2a7f1cd1
https://doi.org/10.1007/s10689-011-9456-8
https://doi.org/10.1007/s10689-011-9456-8
Publikováno v:
Journal of Genetic Counseling. 19:360-370
In families with hereditary breast and ovarian cancer, there is limited knowledge about the reactions of BRCA1/2 mutation positive males. In the present qualitative study, fifteen BRCA1/2 mutation positive men in Norway participated in two successive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f2b61b8803183a008114b0bdb3af23e
https://doi.org/10.1007/s10897-010-9293-1
https://doi.org/10.1007/s10897-010-9293-1
Autor:
Karin Nordin, Mats Hansson, Gunilla Berglund, Eva Gjengedal, Nina Strømsvik, Lars Fredrik Engebretsen
Publikováno v:
Journal of Genetic Counseling. 16:105-117
This qualitative study explores how 29 Swedish patients with Multiple Endocrine Neoplasia type 1 (MEN1) experience living with the condition, appraisal of the clinical follow-up program, and surveys their future expectations. The aim of this study is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78ccea1ad8ae967b722a9bced9c9978a
https://doi.org/10.1007/s10897-006-9047-2
https://doi.org/10.1007/s10897-006-9047-2
Publikováno v:
Familial cancer. 8(3)
Little is known about men seeking genetic counseling for hereditary breast and ovarian cancer (HBOC). We review the sparse literature on men attending such genetic consultations. Two main themes are identified: the women’s influence on the genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3cb223a849c85b9407ac31b2d5f983c
https://pubmed.ncbi.nlm.nih.gov/19165626
https://pubmed.ncbi.nlm.nih.gov/19165626