Works matching IS 17312302 AND DT 2024 AND VI 22 AND IP 1
Results: 27
BRCA2 germline mutation carrier with five malignancies: a case report.
- Published in:
- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00302-7
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- Article
Breast cancer and ATM mutations: treatment implications.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00300-9
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- Publication type:
- Article
A genome-wide association study in Swedish colorectal cancer patients with gastric- and prostate cancer in relatives.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00299-z
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- Article
Meeting abstracts from the Annual Conference "Clinical Genetics of Cancer 2023".
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00294-4
- Publication type:
- Article
Validation of a guidelines-based digital tool to assess the need for germline cancer genetic testing.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00298-0
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- Publication type:
- Article
Molecular analysis of BRCA1 and BRCA2 genes in La Rioja (Spain): five new variants.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00296-2
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- Publication type:
- Article
Current advances and challenges in Managing Hereditary Diffuse Gastric Cancer (HDGC): a narrative review.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00293-5
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- Publication type:
- Article
Current advances and challenges in Managing Hereditary Diffuse Gastric Cancer (HDGC): a narrative review.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00293-5
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- Publication type:
- Article
PMS2 mutation spectra in Norway and risk of cancer for carriers of pathogenic variants.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00292-6
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- Publication type:
- Article
Blood molybdenum level as a marker of cancer risk on BRCA1 carriers.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00291-7
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- Publication type:
- Article
Universal screening of colorectal tumors for lynch syndrome: a survey of patient experiences and opinions.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00290-8
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- Publication type:
- Article
Adrenal tumours in patients with pathogenic APC mutations: a retrospective study.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00289-1
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- Publication type:
- Article
Fear of cancer recurrence in breast cancer survivors carrying a BRCA1 or 2 genetic mutation : a cross-sectional study.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00285-5
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- Publication type:
- Article
Possible link between familial susceptibility to cancer and the level of oxidative stress in thyroid cancer patients.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00287-3
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- Publication type:
- Article
The risk of skin cancer in women who carry BRCA1 or BRCA2 mutations.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00277-5
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- Publication type:
- Article
Information needs of Lynch syndrome and BRCA 1/2 mutation carriers considering risk-reducing gynecological surgery: a qualitative study of the decision-making process.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00278-4
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- Publication type:
- Article
Current prospects of hereditary adrenal tumors: towards better clinical management.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00276-6
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- Publication type:
- Article
Preoperative multimodal ultrasonic imaging in a case of Peutz-Jeghers syndrome complicated by atypical lobular endocervical glandular hyperplasia: a case report and literature review.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00275-7
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- Publication type:
- Article
Universal testing in endometrial cancer in Sweden.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00288-2
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- Publication type:
- Article
Benefits of osimertinib treat a lung adenocarcinoma patient with germline EGFR T790M, somatic EGFR 19-Del, TP53 and PIK3CA mutations.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00286-4
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- Publication type:
- Article
Gastrointestinal manifestations in patients with gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): a systematic review with analysis of individual patient data.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00284-6
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- Publication type:
- Article
Two Japanese families with familial pancreatic cancer with suspected pathogenic variants of CDKN2A: a case report.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00283-7
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- Publication type:
- Article
Modifiable risk factors for cancer among people with lynch syndrome: an international, cross-sectional survey.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00280-w
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- Publication type:
- Article
Mutations in Helicobacter pylori infected patients with chronic gastritis, intestinal type of gastric cancer and familial gastric cancer.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00282-8
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- Publication type:
- Article
A second hereditary cancer predisposition syndrome in a patient with lynch syndrome and three primary cancers.
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- 2024
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- Publication type:
- Case Study
Incidences of colorectal adenomas and cancers under colonoscopy surveillance suggest an accelerated "Big Bang" pathway to CRC in three of the four Lynch syndromes.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00279-3
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- Publication type:
- Article
Li-Fraumeni syndrome presenting with de novo TP53 mutation, severe phenotype and advanced paternal age: a case report.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-023-00272-2
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- Publication type:
- Article