Works matching IS 17312302 AND DT 2023 AND VI 21 AND IP 1
Results: 28
Experiences of patients and family members with follow-up care, information needs and provider support after identification of Lynch Syndrome.
- Published in:
- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00273-1
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- Article
SMAD4 variants and its genotype–phenotype correlations to juvenile polyposis syndrome.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00267-z
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- Article
Choices for cancer prevention for women with a BRCA1 mutation? a personal view.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00271-3
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- Article
Progression of duodenal neoplasia to advanced adenoma in patients with familial adenomatous polyposis.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00264-2
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- Article
"Go ahead and screen" - advice to healthcare systems for routine lynch syndrome screening from interviews with newly diagnosed colorectal cancer patients.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00270-4
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- Article
Simultaneous bilateral mastectomy and RRSO for BRCA2-positive non-invasive breast cancer in Japan: a case report and analysis of initial experience.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00268-y
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- Article
Prevalence of BRCA1 and BRCA2 germline variants in an unselected pancreatic cancer patient cohort in Pakistan.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00269-x
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- Article
Diagnosis of patients with Lynch syndrome lacking the Amsterdam II or Bethesda criteria.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00266-0
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- Article
The prevalence of lynch syndrome (DNA mismatch repair protein deficiency) in patients with primary localized prostate cancer using immunohistochemistry screening.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00265-1
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- Article
Dominantly inherited micro-satellite instable cancer – the four Lynch syndromes - an EHTG, PLSD position statement.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00263-3
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- Article
Periampullary tumors in a patient with pancreatic divisum and neurofibromatosis type 1: a case report.
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- 2023
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- Publication type:
- Case Study
Familial pancreatic cancer: a case study and review of the psychosocial effects of diagnoses on families.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00261-5
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- Publication type:
- Article
A novel pathogenic frameshift variant in AXIN2 in a man with polyposis and hypodontia.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00260-6
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- Article
Factors affecting adherence to a high-risk surveillance protocol among patients with Li-Fraumeni syndrome.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00259-z
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- Publication type:
- Article
Using a multistep approach with multidisciplinary team to increase the diagnosis rate of Lynch syndrome-associated colorectal cancer after universal screening: a single-center study in Japan.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00258-0
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- Article
Lynch-like syndrome with germline WRN mutation in Bulgarian patient with synchronous endometrial and ovarian cancer.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00257-1
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- Article
Meeting abstracts from the Annual Conference "Clinical Genetics of Cancer 2022".
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00253-5
- Publication type:
- Article
BRCA1/2 potential founder variants in the Jordanian population: an opportunity for a customized screening panel.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00256-2
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- Article
Genotype–phenotype correlation of BMPR1a disease causing variants in juvenile polyposis syndrome.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00255-3
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- Article
Genetic testing for hereditary breast cancer in Poland: 1998–2022.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00252-6
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- Article
Beyond germline genetic testing - heterozygous pathogenic variants in PMS2 in two children with Osteosarcoma and Ependymoma.
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- 2023
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- Publication type:
- Case Study
Size matters in telomere biology disorders ‒ expanding phenotypic spectrum in patients with long or short telomeres.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00251-7
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- Article
Comparing telemedicine and in-person gastrointestinal cancer genetic appointment outcomes during the COVID-19 pandemic.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00250-8
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- Article
COVID-19 vaccination uptake and safety profile among germline BRCA1 and BRCA2 pathogenic variant carriers in Singapore.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00248-2
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- Article
Pathological complete response to neoadjuvant chemotherapy in triple negative breast cancer – single hospital experience.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00249-1
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- Article
Are population level familial risks and germline genetics meeting each other?
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00247-3
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- Article
Germline heterozygous exons 8–11 pathogenic BARD1 gene deletion reported for the first time in a family with suspicion of a hereditary colorectal cancer syndrome: more than an incidental finding?
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00246-4
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- Article
The complementary roles of genome-wide approaches in identifying genes linked to an inherited risk of colorectal cancer.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00245-5
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- Article