Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Anne-Marie Axø Gerdes"'
Autor:
Ming Tan, Klaus Brusgaard, Anne-Marie Axø Gerdes, Michael Bau Mortensen, Sönke Detlefsen, Schaffalitzky Muckadell, Ove B., Maiken Thyregod Jørgensen
Publikováno v:
Tan, M, Brusgaard, K, Gerdes, A-M A, Mortensen, M B, Detlefsen, S, Schaffalitzky, O B & Jørgensen, M T 2021, ' Whole genome sequencing identifies rare variants enriched in cancer related genes in first-degree relatives of familial pancreatic cancer patients (Best Poster Award) ', 53rd meeting of the European Pancreatic Club, Verona, Italy, 09/06/2021-11/06/2021 .
University of Southern Denmark
University of Southern Denmark
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a8ff71ec7641c040064274dcd22dd829
https://portal.findresearcher.sdu.dk/da/publications/808f0c43-0ac9-47c4-92ca-7739bb2b468e
https://portal.findresearcher.sdu.dk/da/publications/808f0c43-0ac9-47c4-92ca-7739bb2b468e
Autor:
Vibe Madsen, Smed, Olav Bennike Bjørn, Petersen, Anne-Marie Axø, Gerdes, Birgitte Rode, Diness, Laura Sønderberg, Roos
Publikováno v:
Ugeskrift for laeger. 183(13)
Risk of genetic diseases with autosomal recessive or X-linked inheritance can be unknown to prospective parents until an affected child is born. New technology has enabled carrier screening for hundreds of genetic diseases (expanded carrier screening
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2f23d88f9a4f3cebdfe08deed42762d2
https://pubmed.ncbi.nlm.nih.gov/33829993
https://pubmed.ncbi.nlm.nih.gov/33829993
Autor:
Tanja Røhmer, Wriedt, Anne-Marie Axø, Gerdes, Laura Kristine, Roos, Sophia, Hammer-Hansen, Maja Bejerholm, Christensen, Birgitte Rode, Diness
Publikováno v:
Ugeskrift for laeger. 183(13)
Information regarding hereditary disease predisposition is generally inaccessible for adoptees. The lack of family history restricts access to various surveillance programmes and the overall health of the adoptee. Genetic screening of asymptomatic ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4b8ca8d17a62f635922028063ed21f1a
https://pubmed.ncbi.nlm.nih.gov/33829992
https://pubmed.ncbi.nlm.nih.gov/33829992
Autor:
Vibe Madsen Smed, Olav Petersen, Anne-Marie Axø Gerdes, Birgitte Rode Diness, Laura Sønderberg Roos
Publikováno v:
Smed, V M, Petersen, O B B, Gerdes, A-M A, Diness, B R & Roos, L S 2021, ' Genetisk screening af kommende forældre ', Ugeskrift for Laeger, bind 183, nr. 13, V12200933 . < https://content.ugeskriftet.dk/sites/default/files/scientific_article_files/2021-03/v12200933_web.pdf >
Capital Region of Denmark
Capital Region of Denmark
Risk of genetic diseases with autosomal recessive or X-linked inheritance can be unknown to prospective parents until an affected child is born. New technology has enabled carrier screening for hundreds of genetic diseases (expanded carrier screening
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6dfa0ec3e42e0092abde496e0d657971
https://curis.ku.dk/ws/files/337306663/v12200933_web.pdf
https://curis.ku.dk/ws/files/337306663/v12200933_web.pdf
Publikováno v:
Ugeskrift for laeger. 179(11)
Direct-to-consumer genetic tests are sold over the internet to consumers all over the world - including Denmark. No regulation of these tests has been introduced neither in Denmark nor in Europe, even though they have been on the market since 2007. S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3887640e1164689cefe2e18e26059511
https://pubmed.ncbi.nlm.nih.gov/28330535
https://pubmed.ncbi.nlm.nih.gov/28330535
Autor:
Marie Louise Mølgaard Binderup, Søs Marie Luise Bisgaard, Vibeke Harbud, Hans Ulrik Møller, Steen Gimsing, Lennart Jan Friis-Hansen, Thomas van Overeem Hansen, Per Bagi, Ulrich Knigge, Michael Kosteljanetz, Lars Bøgeskov, Carsten Thomsen, Anne-Marie Axø Gerdes, Lillian Bomme Ousager, Lone Sunde
Publikováno v:
Aarhus University
Binderup, M L M, Bisgaard, S M L, Harbud, V, Møller, H U, Gimsing, S, Friis-Hansen, L J, Hansen, T V O, Bagi, P, Knigge, U, Kosteljanetz, M, Bøgeskov, L, Thomsen, C, Gerdes, A-M A, Ousager, L B & Sunde, L 2013, ' Von Hippel-Lindau disease (vHL). National clinical guideline for diagnosis and surveillance in Denmark. 3rd edition ', Danish Medical Journal, vol. 60, no. 12, pp. B4763 .
Binderup, M L M, Bisgaard, S M L, Harbud, V, Møller, H U, Gimsing, S, Friis-Hansen, L J, Hansen, T V O, Bagi, P, Knigge, U, Kosteljanetz, M, Bøgeskov, L, Thomsen, C, Gerdes, A-M A, Ousager, L B & Sunde, L 2013, ' Von Hippel-Lindau disease (vHL). National clinical guideline for diagnosis and surveillance in Denmark. 3rd edition ', Danish Medical Journal, vol. 60, no. 12, pp. B4763 .
These clinical guidelines outline the criteria and recommendations for diagnostic and genetic work-up of families suspected of von Hippel-Lindau disease (vHL), as well as recommendations for prophylactic surveillance for vHL patients. The guideline h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::fb5a061663542d6fbeb141cd2dde5472
https://pubmed.ncbi.nlm.nih.gov/24355456
https://pubmed.ncbi.nlm.nih.gov/24355456
Publikováno v:
Ugeskrift for laeger. 174(8)
Denmark is a high-risk country for malignant melanoma (MM).The incidence of MM has increased faster than the ones of any other cancer during the last ten years. 5-10% of the patients with MM report a family history of MM, and this is most likely caus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6d03a258541808b81c7b7af99f249ef0
https://pubmed.ncbi.nlm.nih.gov/22348671
https://pubmed.ncbi.nlm.nih.gov/22348671
Autor:
Anne-Marie Axø, Gerdes
Publikováno v:
Ugeskrift for laeger. 173(34)
Hereditary cancer syndromes are characterized by increased risk of cancers but other symptoms can also be seen. Germline mutations usually cause a high cancer risk but more moderate risk genes are being identified. A negative mutation screening canno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::529c664b3454cd2e4dbfa8a1afc6f964
https://pubmed.ncbi.nlm.nih.gov/21867655
https://pubmed.ncbi.nlm.nih.gov/21867655
Autor:
Anne-Marie Axø, Gerdes
Publikováno v:
Ugeskrift for laeger. 164(22)
Genetic changes are associated with the neoplastic process, when a normal cell is transformed into a cancer cell. Cell growth and differentiation are regulated by complicated interactions between growth promoting and inhibiting signals. Oncogenes are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::23750c59ecf564d199d0919b8a05517d
https://pubmed.ncbi.nlm.nih.gov/12082811
https://pubmed.ncbi.nlm.nih.gov/12082811
Autor:
Ming Tan, Klaus Brusgaard, Anne-Marie Axø Gerdes, Michael Bau Mortensen, Sönke Detlefsen, Ove B Schaffalitzky de Muckadell, Maiken Thyregod Jørgensen
Publikováno v:
University of Southern Denmark
Tan, M, Brusgaard, K, Gerdes, A-M A, Mortensen, M B, Detlefsen, S, Schaffalitzky, O B & Jørgensen, M T 2021, ' Heritability of Familial Pancreatic Cancer in a Danish national family cohort (Su293) ', Digestive Disease Week 2021, Washington D.C., United States, 21/05/2021-23/05/2021 .
Tan, M, Brusgaard, K, Gerdes, A-M A, Mortensen, M B, Detlefsen, S, Schaffalitzky, O B & Jørgensen, M T 2021, ' Heritability of Familial Pancreatic Cancer in a Danish national family cohort (Su293) ', Digestive Disease Week 2021, Washington D.C., United States, 21/05/2021-23/05/2021 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1b45f20908128f54a2317ea4a41f8072
https://portal.findresearcher.sdu.dk/en/publications/6a6f2594-1510-4d44-a358-259e161bdf37
https://portal.findresearcher.sdu.dk/en/publications/6a6f2594-1510-4d44-a358-259e161bdf37