Suchergebnisse - "Vetti, Hildegunn Høberg"

PubPharm (11)

1

Evaluation of the Rosa Chatbot Providing Genetic Information to Patients at Risk of Hereditary Breast and Ovarian Cancer : Qualitative Interview Study

enthalten in: Journal of medical Internet research | 2023

von Siglen, E. | Vetti, H. | Augestad, M. | +3

2

The PTEN hamartoma tumor syndrome : how oral clinicians may save lives

enthalten in: Clinical advances in periodontics | 2023

von Fardal, �. | Nevland, K. | Johannessen, A. | +1

3

The PTEN hamartoma tumor syndrome : how oral clinicians may save lives

enthalten in: Clinical Advances in Periodontics | 2023

von Fardal, �. | Nevland, K. | Johannessen, A. | +1

4

Ask Rosa - The making of a digital genetic conversation tool, a chatbot, about hereditary breast and ovarian cancer

enthalten in: Patient education and counseling | 2022

von Siglen, E. | Vetti, H. | Lunde, A. | +7

5

Overview of hereditary breast and ovarian cancer (HBOC) guidelines across Europe

enthalten in: European journal of medical genetics | 2021

von Marmolejo, D. | Wong, M. | Bajalica-Lagercrantz, S. | +19

6

Gastric adenocarcinoma and proximal polyposis of the stomach – a rare form of hereditary gastric cancer

enthalten in: Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke | 2020

von Mala, T. | Førland, D. | Vetti, H. | +3

7

Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88 defect

enthalten in: Familial cancer | 2016

von Vogelaar, I. | Ligtenberg, M. | van der Post, R. | +30

8

Risk reducing mastectomy, breast reconstruction and patient satisfaction in Norwegian BRCA1/2 mutation carriers

enthalten in: Breast (Edinburgh, Scotland) | 2014

von Hagen, A. | Mæhle, L. | Vedå, N. | +10

9

Risk reducing mastectomy, breast reconstruction and patient satisfaction in Norwegian BRCA1/2 mutation carriers

enthalten in: The breast | 2014

von Hagen, A. | Mæhle, L. | Vedå, N. | +10

10

Melanoma prone families with CDK4 germline mutation : phenotypic profile and associations with MC1R variants

enthalten in: Journal of medical genetics | 2013

von Puntervoll, H. | Yang, X. | Vetti, H. | +30

ErratumIn: J Med Genet. 2014 Mar;51(3):214