Familial Cancer - 2013

101 articles | Last updated: 2025-12-03 14:12:56
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T A T A T A T A
Is intraductal tubulopapillary neoplasia a new entity in the spectrum of familial pancreatic cancer syndrome?
Attitudes and knowledge of medical practitioners to hereditary cancer clinics and cancer genetic testing
Breast cancer risk assessment in 8,824 women attending a family history evaluation and screening programme
Evaluation after five years of the cancer genetic counselling programme of Valencian Community (Eastern Spain)
Ectopic Cushing syndrome associated with thymic carcinoid tumor as the first presentation of MEN1 syndrome-report of a family with MEN1 gene mutation
A randomized controlled trial of diet and physical activity in BRCA mutation carriers
RAD51 135G>C and TP53 Arg72Pro polymorphisms and susceptibility to breast cancer in Serbian women
Inversion of exons 1–7 of the MSH2 gene is a frequent cause of unexplained Lynch syndrome in one local population
Impact of familial risk and mammography screening on prognostic indicators of breast disease among women from the Ontario site of the Breast Cancer Family Registry
Misperceptions of ovarian cancer risk in women at increased risk for hereditary ovarian cancer
Birt–Hogg–Dubé syndrome
Comparison of attitudes regarding preimplantation genetic diagnosis among patients with hereditary cancer syndromes
Diversity of the clinical presentation of the MMR gene biallelic mutations
More breast cancer patients prefer BRCA-mutation testing without prior face-to-face genetic counseling
Abstracts
Prevalence of PALB2 mutation c.509_510delGA in unselected breast cancer patients from Central and Eastern Europe
Genetic variation at 8q24, family history of cancer, and upper gastrointestinal cancers in a Chinese population
Cancer risk and overall survival in mismatch repair proficient hereditary non-polyposis colorectal cancer, Lynch syndrome and sporadic colorectal cancer
Reflex testing for Lynch syndrome: If we build it, will they come? Lessons learned from the uptake of clinical genetics services by individuals with newly diagnosed colorectal cancer (CRC)
Impact of breast cancer family history on tumor detection and tumor size in women newly-diagnosed with invasive breast cancer
Illness perceptions, risk perception and worry in SDH mutation carriers
Lynch Syndrome in high risk Ashkenazi Jews in Israel Ashkenazi Jews
Lack of association between let-7 binding site polymorphism rs712 and risk of nasopharyngeal carcinoma
Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families
Does and should breast cancer genetic counselling include lifestyle advice?
Cancer risk and genotype–phenotype correlations in PTEN hamartoma tumor syndrome
Erratum to: Birt–Hogg–Dubé: beyond the clinical manifestations
InSiGHT, pedigree, familial aspects of cancer and the Human Variome Project in conjunction with the COSA familial cancer group
Chemoprevention in Lynch syndrome
The MDM2 285G–309G haplotype is associated with an earlier age of tumour onset in patients with Li-Fraumeni syndrome
Endometrial tumour BRAF mutations and MLH1 promoter methylation as predictors of germline mismatch repair gene mutation status: a literature review
No evidence of genetic anticipation in a large family with Lynch syndrome
Barrett’s esophagus in the patients with familial adenomatous polyposis
Towards a vaccine to prevent cancer in Lynch syndrome patients
Endometrial and ovarian cancer in women with Lynch syndrome: update in screening and prevention
Whole exome sequencing identifies mutation of EDNRA involved in ACTH-independent macronodular adrenal hyperplasia
The prevalence of small intestinal polyps in patients with familial adenomatous polyposis: a prospective capsule endoscopy study
MAX mutations status in Swedish patients with pheochromocytoma and paraganglioma tumours Swedish patients
Mammographic surveillance in women aged 35–39 at enhanced familial risk of breast cancer (FH02)
Multivariate analysis of MLH1 c.1664T>C (p.Leu555Pro) mismatch repair gene variant demonstrates its pathogenicity
Pulmonary manifestations of Birt-Hogg-Dubé syndrome
Polymorphisms in arachidonic acid metabolism-related genes and the risk and prognosis of colorectal cancer
Surveillance for urinary tract cancer in Lynch syndrome
Screening participation for people at increased risk of colorectal cancer due to family history: a systematic review and meta-analysis
Diagnosis and management of BHD-associated kidney cancer
Value-based healthcare in Lynch syndrome
Rectal cancers in patients with familial adenomatous polyposis
100 years lynch syndrome: what have we learned about psychosocial issues?
A hundred years of Lynch syndrome research (1913–2013)
Phenotypic heterogeneity of hereditary gynecologic cancers: a report from the Creighton hereditary cancer registry
“High rate of recurrent adenomatosis during endoscopic surveillance after duodenectomy in patients with familial adenomatous polyposis”
Foreword for “100 years of Lynch syndrome”
Do lifestyle factors influence colorectal cancer risk in Lynch syndrome?
Association of the BRCA1 promoter polymorphism rs11655505 with the risk of familial breast and/or ovarian cancer
Underestimated survival predictions of the prognostic tools Adjuvant! Online and PREDICT in BRCA1-associated breast cancer patients
The Proceedings of the Collaborative Group of the Americas on Inherited Colorectal Cancer Sheraton Boston Hotel, Boston, Massachusetts, October 27–29, 2012
Case report: metachronous central nervous system desmoid tumours and thyroid carcinoma in a young familial adenomatous polyposis patient
Cancer risk in Lynch Syndrome
Can we test for hereditary cancer at 18 years when we start surveillance at 25? Patient reported outcomes
Extracolonic cancer risk in patients with serrated polyposis syndrome and their first-degree relatives
The mechanism of mismatch repair and the functional analysis of mismatch repair defects in Lynch syndrome
How do we approach the goal of identifying everybody with Lynch Syndrome?
Self administered screening for hereditary cancers in conjunction with mammography and ultrasound
Do individuals with a family history of colorectal cancer adhere to medical recommendations for the prevention of colorectal cancer?
The History of Lynch Syndrome
Prediction models in Lynch syndrome
Chemotherapy of MMR-deficient colorectal cancer
Informing family members of individuals with Lynch syndrome: a guideline for clinical geneticists
Lynch syndrome: the patients perspective
Gene variants of unknown clinical significance in Lynch syndrome. An introduction for clinicians
Colorectal surveillance in Lynch syndrome families
Psychosocial consequences of predictive genetic testing for lynch syndrome and associations to surveillance behaviour in a 7-year follow-up study
Surgical treatment of hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome)
Interest of individuals from BRCA families to participate in research studies focused on male BRCA carriers
Factors affecting the decision to undergo risk-reducing salpingo-oophorectomy among women with BRCA gene mutation
Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome
Novel and recurrent BRCA1/BRCA2 mutations in early onset and familial breast and ovarian cancer detected in the Program of Genetic Counseling in Cancer of Valencian Community (eastern Spain). Relation
Is the psychological impact of genetic testing moderated by support and sharing of test results to family and friends?
Prevalence of HOXB13 mutation in a population of Ashkenazi Jewish men treated for prostate cancer Ashkenazi Jewish
Genetic modifiers of cancer risk in Lynch syndrome: a review
The incidence of PALB2 c.3113G>A in women with a strong family history of breast and ovarian cancer attending familial cancer centres in Australia
Clinical characterization and mutation spectrum in Hispanic families with adenomatous polyposis syndromes
The role of epigenetics in Lynch syndrome
The InSiGHT database: utilizing 100 years of insights into Lynch Syndrome
Lynch syndrome-associated neoplasms: a discussion on histopathology and immunohistochemistry
Role of new endoscopic techniques in Lynch syndrome
Preparing individuals to communicate genetic test results to their relatives: report of a randomized control trial
Mutation screen and RNA analysis disclose the changed splicing of the E-cadherin transcription in gastric cancer
13th International Meeting on Psychosocial Aspects of Hereditary Cancer (IMPAHC)
Familial adenomatous polyposis: not all masses are desmoids
Detection of large deletions in the VHL gene using a Real-Time PCR with SYBR Green
The prognostic value of MGMT promoter methylation in Glioblastoma multiforme: a meta-analysis
Mutation screening in a Norwegian cohort with pheochromocytoma
Erratum to: Closing the loop: an interactive action research conference format for delivering updated medical information while eliciting Latina patient/family experiences and psychosocial needs post-
Erratum to: Evaluating Lynch syndrome in very early onset colorectal cancer probands without apparent polyposis
GNAS is not involved in gastrointestinal tumour formation in Peutz-Jeghers syndrome
Splice site mutations in mismatch repair genes and risk of cancer in the general population
Erratum to: Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
The risk of gastric cancer in carriers of CHEK2 mutations
Birt–Hogg–Dubé syndrome and the skin
Detection of large scale 3′ deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything?