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1. Mutations in SDHD are the major determinants of the clinical characteristics of Dutch head and neck paraganglioma patients

2. Risks of Lynch Syndrome Cancers for MSH6 Mutation Carriers

3. Genetic testing in Li-Fraumeni syndrome: uptake and psychosocial consequences

4. Increased Urinary Excretion of 3-Methoxytyramine in Patients with Head and Neck Paragangliomas

5. Regular surveillance for Li-fraumeni syndrome: advice, adherence and perceived benefits

6. Molecular characterization of novel germline deletions affecting SDHD and SDHC in pheochromocytoma and paraganglioma patients

7. Malignant Paragangliomas Associated with Mutations in the Succinate Dehydrogenase D Gene

8. Heterozygous Mutations in PMS2 Cause Hereditary Nonpolyposis Colorectal Carcinoma (Lynch Syndrome)

9. Head-and-neck paragangliomas are associated with sleep-related complaints, especially in the presence of carotid body tumors

10. Normal Life Expectancy for Paraganglioma Patients: A 50-Year-Old Cohort Revisited

11. Pheochromocytomas detected by biochemical screening in predisposed subjects are associated with lower prevalence of clinical and biochemical manifestations and smaller tumors than pheochromocytomas detected by signs and symptoms

12. The Dutch founder mutation SDHD.D92Y shows a reduced penetrance for the development of paragangliomas in a large multigenerational family

13. Quantification of Sequence Exchange Events between PMS2 and PMS2CL Provides a Basis for Improved Mutation Scanning of Lynch Syndrome Patients

14. Low penetrance of a SDHB mutation in a large Dutch paraganglioma family

15. Psychological distress and use of psychosocial support in familial adenomatous polyposis

16. The first Dutch SDHB founder deletion in paraganglioma – pheochromocytoma patients

18. Attitude towards pre-implantation genetic diagnosis for hereditary cancer

19. Pheochromocytomas and extra-adrenal paragangliomas detected by screening in patients with SDHD-associated head-and-neck paragangliomas

20. Reduced quality of life in patients with head-and-neck paragangliomas

21. Molecular characterization of novel germline deletions affecting SDHD and SDHC in pheochromocytoma and paraganglioma patients.

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