Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Awareness of heredity in colorectal cancer patients is insufficient among clinicians: a Norwegian population-based study.

Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland - 1 Jun 2009

Tranø G, Wasmuth H H, Sjursen W, Hofsli E, Vatten L J

Abstract excerpt

OBJECTIVE: The assessment of family history and medical data is crucial in identifying families with Lynch syndrome (LS). Among consecutive colorectal cancer (CRC) patients, we aimed at identifying all patients with a hereditary predisposition, and to study a possible discrepancy with assessments...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged
Share to Aged, 80 and over
Share to Cohort Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Colorectal Neoplasms

Share to Colorectal Neoplasms, Hereditary Nonpolyposis

Share to Family Health

Share to Norway

Share to Practice Guidelines as Topic

Source

Identifiers

PMID: 19508550
DOI: 10.1111/j.1463-1318.2009.01830.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19508550-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Awareness of heredity in colorectal cancer patients is insufficient among clinicians: a Norwegian population-based study.PMID 19508550Read ↗

Family history is neglected in the work-up of patients with colorectal cancer: a quality assessment using cancer registry data.Semantic proximity Read ↗

Patient and tumor characteristics may raise clinicians' awareness of familial colorectal cancer: a Norwegian population-based study.Semantic proximity Read ↗

Hereditary evaluation and genetic counselling in young individuals with colorectal cancer in a population-based cohort.Semantic proximity Read ↗

Recording of family history is associated with colorectal cancer stage.Semantic proximity Read ↗

Identification of patients at-risk for Lynch syndrome in a hospital-based colorectal surgery clinic.Semantic proximity Read ↗

Hereditary nonpolyposis colorectal carcinoma (HNPCC) and HNPCC-like families: Problems in diagnosis, surveillance, and management.Semantic proximity Read ↗

Informing family members of individuals with Lynch syndrome: a guideline for clinical geneticists.Semantic proximity Read ↗

Performance of clinical guidelines compared with molecular tumour screening methods in identifying possible Lynch syndrome among colorectal cancer patients: a Norwegian population-based study.Semantic proximity Read ↗

Family and personal history in colorectal cancer patients: what are we missing?Semantic proximity Read ↗

Improving the uptake of predictive testing and colorectal screening in Lynch syndrome: a regional primary care survey.Semantic proximity Read ↗

Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels.Semantic proximity Read ↗

Familial colorectal cancer: a concept revisited.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.