Works matching IS 13899600 AND DT 2025 AND VI 24 AND IP 1
Results: 27
Optimizing MRI sequences and apparent diffusion coefficient parameters for small pancreatic ductal adenocarcinoma detection.
- Published in:
- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00447-x
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- Article
Addressing uncertainty in hereditary colorectal cancer: the role of a regional expert multidisciplinary team meeting.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00451-1
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- Article
Healthcare provider-mediated cascade testing of Lynch syndrome to at-risk family members: an interview study.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00450-2
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- Article
A novel likely pathogenic germline variant in CDKN1B in a patient with MEN4 and medullary thyroid cancer.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00449-9
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- Article
CHEK2-related breast cancer: real-world challenges.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00448-w
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- Article
New RPS20 gene variant in colorectal cancer diagnosis: insight from a large series of patients.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00446-y
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- Article
Identification of a germline deep intronic PTEN-deletion leading to exonization through whole genome and targeted RNA sequencing.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00445-z
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- Article
Myelodysplastic syndrome with dual germline RUNX1 and DDX41 variants: a rare genetic predisposition case.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00443-1
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- Article
Thirty-year compliance with a surveillance program for patients with familial adenomatous polyposis.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00441-3
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- Article
Case review of perivascular epithelioid cell tumor occurring in patients with Li-Fraumeni syndrome.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00442-2
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- Article
Correction: Outcomes of retesting in patients with previously uninformative cancer genetics evaluations.
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- 2025
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- Correction Notice
Progress report on multiple endocrine neoplasia type 1.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00440-4
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- Article
Correction: Benign tumors and non-melanoma skin cancers in patients with fanconi anemia.
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- 2025
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- Publication type:
- Correction Notice
The challenge of preventing gastric cancer in patients under surveillance for familial adenomatous polyposis.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00438-4
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- Publication type:
- Article
Haplotype analysis detects MLH1 founder variant in Indian Lynch syndrome patient cohort.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00436-6
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- Article
Bilateral familial retinoblastoma diagnosed via optical coherence tomography following a normal funduscopic exam.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00424-w
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- Article
Recurrent paraneoplastic nephrotic syndrome; insights from a Lynch syndrome patient with multiple malignancies.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00435-7
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- Article
Sarcomas arising in MEN1 patients: demonstrating LOH of the MEN1 locus and loss of menin expression.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00433-9
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- Article
A family-based approach to cascade genetic testing in a pediatric cancer genetics clinic.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00434-8
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- Article
Cascade genetic testing in hereditary cancer: exploring the boundaries of the Italian legal framework.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00430-y
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- Article
Hereditary breast and ovarian cancer genetic testing in unselected patients: example of private supplementation of public healthcare service.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00426-8
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- Article
Overlap syndrome of hereditary hemorrhagic telangiectasia and juvenile polyposis syndrome: ten years follow-up-case series and review of literature.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00425-9
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- Article
Prevalence of cardiometabolic outcomes in women who underwent salpingo-oophorectomy to prevent hereditary breast and ovarian cancer: a meta-analysis.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00431-x
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- Article
BRCAIndica: a resource for ACMG/AMP classified BRCA1 and BRCA2 variants.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00429-5
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- Article
Germline pathogenic variants in RNF43 in patients with and without serrated polyposis syndrome.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00428-6
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- Publication type:
- Article
Mainstreaming cancer genetics: feasibility of an advanced nurse practitioner-led service diagnosing Lynch syndrome from colorectal cancer in Ireland.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00427-7
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- Publication type:
- Article
The genetic landscape of Lynch syndrome in the Israeli population.
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- Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00432-w
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- Article