Found: 29
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The pathogenesis of pneumothorax in Birt- Hogg- Dubé syndrome: A hypothesis.
- Published in:
- 2014
- By:
- Publication type:
- Other
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
- By:
- Publication type:
- Article
Survival after adjuvant 5-FU treatment for stage III colon cancer in hereditary nonpolyposis colorectal cancer.
- Published in:
- International Journal of Cancer, 2004, v. 109, n. 3, p. 468, doi. 10.1002/ijc.11712
- By:
- 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.
- Published in:
- Patient Preference & Adherence, 2020, v. 14, p. 333, doi. 10.2147/PPA.S232941
- By:
- Publication type:
- Article
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
- By:
- Publication type:
- 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
- By:
- Publication type:
- Article
Re: Germline BRCA1 mutations and a basal epithelial phenotype in breast cancer.
- Published in:
- 2004
- By:
- Publication type:
- letter
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
- By:
- 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
- By:
- Publication type:
- Article
Spontaneous pneumothorax as indicator for Birt-Hogg-Dubé syndrome in paediatric patients.
- Published in:
- 2014
- By:
- Publication type:
- journal 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
- By:
- 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
- By:
- 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
- By:
- Publication type:
- Article
Dysplastic changes in prophylactically removed Fallopian tubes of women predisposed to developing ovarian cancer.
- Published in:
- Journal of Pathology, 2001, v. 195, n. 4, p. 451, doi. 10.1002/path.1000
- By:
- Publication type:
- Article
CDC73-Related Disorders: Clinical Manifestations and Case Detection in Primary Hyperparathyroidism.
- Published in:
- 2017
- By:
- Publication type:
- journal article
In-Flight Pneumothorax: Diagnosis May Be Missed because of Symptom Delay.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2014, v. 190, n. 6, p. 704, doi. 10.1164/rccm.201404-0698le
- By:
- Publication type:
- Article
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
- By:
- Publication type:
- Article
A new locus-specific database (LSDB) for mutations in the folliculin ( FLCN) gene.
- Published in:
- 2010
- By:
- Publication type:
- Other
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
- By:
- Publication type:
- Article
Birt-Hogg-Dubé Syndrome: Clinical and Genetic Studies of 20 Families.
- Published in:
- Journal of Investigative Dermatology, 2008, v. 128, n. 1, p. 45, doi. 10.1038/sj.jid.5700959
- By:
- Publication type:
- 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
- By:
- 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
- By:
- Publication type:
- Article
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
- By:
- Publication type:
- 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
- By:
- 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
- By:
- 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.
- Published in:
- Psycho-Oncology, 2012, v. 21, n. 1, p. 29, doi. 10.1002/pon.1864
- By:
- Publication type:
- Article
Biallelic germline mutations of mismatch-repair genes: a possible cause for multiple pediatric malignancies.
- Published in:
- 2007
- By:
- Publication type:
- journal 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
- By:
- 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
- By:
- Publication type:
- journal article