Found: 29
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Does a proactive procedure lead to a higher uptake of predictive testing in families with a pathogenic BRCA1/BRCA2 variant? A family cancer clinic evaluation.
- Published in:
- Journal of Genetic Counseling, 2024, v. 33, n. 3, p. 615, doi. 10.1002/jgc4.1767
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- Publication type:
- Article
Familial Breast Cancer: Clinical Services in the Netherlands.
- Published in:
- Disease Markers, 1999, v. 15, n. 1-3, p. 31, doi. 10.1155/1999/151365
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- Publication type:
- Article
The tumour spectrum in hereditary non-polyposis colorectal cancer: A study of 24 kindreds in the netherlands.
- Published in:
- International Journal of Cancer, 1990, v. 46, n. 1, p. 31, doi. 10.1002/ijc.2910460108
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- Publication type:
- Article
Do Preferred Risk Formats Lead to Better Understanding? A Multicenter Controlled Trial on Communicating Familial Breast Cancer Risks Using Different Risk Formats.
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- Patient Preference & Adherence, 2020, v. 14, p. 333, doi. 10.2147/PPA.S232941
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- Publication type:
- Article
Dysplastic changes in prophylactically removed Fallopian tubes of women predisposed to developing ovarian cancer.
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- Journal of Pathology, 2001, v. 195, n. 4, p. 451, doi. 10.1002/path.1000
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- Publication type:
- Article
CDC73-Related Disorders: Clinical Manifestations and Case Detection in Primary Hyperparathyroidism.
- Published in:
- 2017
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- Publication type:
- journal article
Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity.
- Published in:
- PLoS Genetics, 2017, v. 13, n. 5, p. 1, doi. 10.1371/journal.pgen.1006765
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- Publication type:
- Article
Topical Rapamycin as a Treatment for Fibrofolliculomas in Birt-Hogg-Dubé Syndrome: A Double-Blind Placebo-Controlled Randomized Split-Face Trial.
- Published in:
- PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0099071
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- Publication type:
- Article
HIF-1α Overexpression in Ductal Carcinoma In Situ of the Breast in <i>BRCA1</i> and <i>BRCA2</i> Mutation Carriers.
- Published in:
- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0056055
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- Publication type:
- Article
The effectiveness of a graphical presentation in addition to a frequency format in the context of familial breast cancer risk communication: a multicenter controlled trial.
- Published in:
- BMC Medical Informatics & Decision Making, 2013, v. 13, n. 1, p. 1, doi. 10.1186/1472-6947-13-55
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- Publication type:
- Article
The effectiveness of a graphical presentation in addition to a frequency format in the context of familial breast cancer risk communication: a multicenter controlled trial.
- Published in:
- 2013
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- Publication type:
- journal article
Genetic counseling does not fulfill the counselees' need for certainty in hereditary breast/ovarian cancer families: an explorative assessment.
- Published in:
- Psycho-Oncology, 2013, v. 22, n. 5, p. 1167, doi. 10.1002/pon.3125
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- Publication type:
- Article
The counselees' self-reported request for psychological help in genetic counseling for hereditary breast/ovarian cancer: not only psychopathology matters.
- Published in:
- Psycho-Oncology, 2013, v. 22, n. 4, p. 902, doi. 10.1002/pon.3081
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- Publication type:
- Article
Opening the psychological black box in genetic counseling. The psychological impact of DNA testing is predicted by the counselees' perception, the medical impact by the pathogenic or uninformative BRCA1/2-result.
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- Psycho-Oncology, 2012, v. 21, n. 1, p. 29, doi. 10.1002/pon.1864
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- Publication type:
- Article
Re: Germline BRCA1 mutations and a basal epithelial phenotype in breast cancer.
- Published in:
- 2004
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- Publication type:
- Letter
A cost-effectiveness analysis of colorectal screening for hereditary nonpolyposis colorectal carcinoma gene carriers.
- Published in:
- Cancer (0008543X), 1998, v. 82, n. 9, p. 1632, doi. 10.1002/(SICI)1097-0142(19980501)82:9<1632::AID-CNCR6>3.0.CO;2-C
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- Publication type:
- Article
High frequency of HIF-1α overexpression in BRCA1 related breast cancer.
- Published in:
- Breast Cancer Research & Treatment, 2008, v. 111, n. 3, p. 475, doi. 10.1007/s10549-007-9817-z
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- Publication type:
- Article
Biallelic germline mutations of mismatch-repair genes: a possible cause for multiple pediatric malignancies.
- Published in:
- 2007
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- Publication type:
- journal article
Low prevalence of (pre) malignant lesions in the breast and high prevalence in the ovary and Fallopian tube in women at hereditary high risk of breast and ovarian cancer.
- Published in:
- International Journal of Cancer, 2006, v. 119, n. 6, p. 1412, doi. 10.1002/ijc.21988
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- Publication type:
- Article
Survival after adjuvant 5-FU treatment for stage III colon cancer in hereditary nonpolyposis colorectal cancer.
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- International Journal of Cancer, 2004, v. 109, n. 3, p. 468, doi. 10.1002/ijc.11712
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- Publication type:
- Article
Birt-Hogg-Dubé Syndrome: Clinical and Genetic Studies of 20 Families.
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- Journal of Investigative Dermatology, 2008, v. 128, n. 1, p. 45, doi. 10.1038/sj.jid.5700959
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- Publication type:
- Article
In-Flight Pneumothorax: Diagnosis May Be Missed because of Symptom Delay.
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- American Journal of Respiratory & Critical Care Medicine, 2014, v. 190, n. 6, p. 704, doi. 10.1164/rccm.201404-0698le
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- Publication type:
- Article
Spontaneous pneumothorax as indicator for Birt-Hogg-Dubé syndrome in paediatric patients.
- Published in:
- BMC Pediatrics, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-2431-14-171
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- Publication type:
- Article
Spontaneous pneumothorax as indicator for Birt-Hogg-Dubé syndrome in paediatric patients.
- Published in:
- 2014
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- Publication type:
- journal article
Birt–Hogg–Dubé syndrome is a novel ciliopathy.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 21, p. 4383, doi. 10.1093/hmg/ddt288
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- Publication type:
- Article
The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice.
- Published in:
- Familial Cancer, 2019, v. 18, n. 1, p. 127, doi. 10.1007/s10689-018-0089-z
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- Publication type:
- Article
The pathogenesis of pneumothorax in Birt- Hogg- Dubé syndrome: A hypothesis.
- Published in:
- 2014
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- Publication type:
- Other
A new locus-specific database (LSDB) for mutations in the folliculin ( FLCN) gene.
- Published in:
- 2010
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- Publication type:
- Other
Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma.
- Published in:
- BMC Medical Genetics, 2006, v. 7, p. 1, doi. 10.1186/1471-2350-7-1
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- Publication type:
- Article