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Author/Creator Stormorken, Astrid

1. A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study. Issue 11 (November 2021)

Authors:
Bancroft, Elizabeth K; Page, Elizabeth C; Brook, Mark N; Thomas, Sarah; Taylor, Natalie; Pope, Jennifer; McHugh, Jana; Jones, Ann-Britt; Karlsson, Questa; Merson, Susan; Ong, Kai Ren; Hoffman, Jonathan; Huber, Camilla; Maehle, Lovise; Grindedal, Eli Marie; Stormorken, Astrid; Evans, D Gareth; Rot...
Journal:
Lancet oncology
Issue:
Volume 22:Issue 11(2021)
Page Start:
1618
Record Type:
Journal Article
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2. Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers. Issue 9 (28th June 2010)

Authors:
Sjursen, Wenche; Haukanes, Bjørn Ivar; Grindedal, Eli Marie; Aarset, Harald; Stormorken, Astrid; Engebretsen, Lars F; Jonsrud, Christoffer; Bjørnevoll, Inga; Andresen, Per Arne; Ariansen, Sarah; Lavik, Liss Anne S; Gilde, Bodil; Bowitz-Lothe, Inger Marie; Mæhle, Lovise; Møller, Pål
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 9(2010)
Page Start:
579
Record Type:
Journal Article
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3. Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts. Issue 6 (13th February 2013)

Authors:
Vasen, Hans F A; Blanco, Ignacio; Aktan-Collan, Katja; Gopie, Jessica P; Alonso, Angel; Aretz, Stefan; Bernstein, Inge; Bertario, Lucio; Burn, John; Capella, Gabriel; Colas, Chrystelle; Engel, Christoph; Frayling, Ian M; Genuardi, Maurizio; Heinimann, Karl; Hes, Frederik J; Hodgson, Shirley V; Ka...
Other Names:
contributor.
Journal:
Gut
Issue:
Volume 62:Issue 6(2013)
Page Start:
812
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗