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26 results on '"Ausems, M."'

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1. Patients' experiences with pre-test genetic counseling provided by breast cancer healthcare professionals: Results from a large prospective multicenter study.

2. Surgical Oncologists and Nurses in Breast Cancer Care are Ready to Provide Pre-Test Genetic Counseling.

3. Development of a plain-language guide for discussing breast cancer genetic counseling and testing with patients with limited health literacy.

4. Genetic counselling of young women with breast cancer for Li-Fraumeni syndrome: a nationwide survey on the experiences and attitudes of genetics professionals.

5. TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort.

6. Ovarian stimulation for IVF and risk of primary breast cancer in BRCA1/2 mutation carriers.

7. Primary care management of women with breast cancer-related concerns-a dynamic cohort study using a network database.

8. Migrant breast cancer patients and their participation in genetic counseling: results from a registry-based study.

9. Timing of risk reducing mastectomy in breast cancer patients carrying a BRCA1/2 mutation: retrospective data from the Dutch HEBON study.

10. Repeated nipple fluid aspiration: compliance and feasibility results from a prospective multicenter study.

11. Breast cancer risk after salpingo-oophorectomy in healthy BRCA1/2 mutation carriers: revisiting the evidence for risk reduction.

12. Active approach for breast cancer genetic counseling during radiotherapy: long-term psychosocial and medical impact.

13. Impact of rapid genetic counselling and testing on the decision to undergo immediate or delayed prophylactic mastectomy in newly diagnosed breast cancer patients: findings from a randomised controlled trial.

14. Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2.

15. BRCA testing of breast cancer patients: medical specialists' referral patterns, knowledge and attitudes to genetic testing.

17. Predictors of choosing life-long screening or prophylactic surgery in women at high and moderate risk for breast and ovarian cancer.

18. Cancer risks in BRCA2 families: estimates for sites other than breast and ovary.

19. De novo recurrent germline mutation of the BRCA2 gene in a patient with early onset breast cancer.

20. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

21. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

22. An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

23. Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers

24. Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

25. Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

26. Exploring the link between MORF4L1 and risk of breast cancer

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