Works matching Li-Fraumeni syndrome (LFS)
Results: 235
The Li-Fraumeni syndrome (LFS): a model for the initiation of p53 signatures in the distal Fallopian tube.
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- Journal of Pathology, 2010, v. 220, n. 1, p. 17, doi. 10.1002/path.2624
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- Article
Distress in partners of individuals diagnosed with or at high risk of developing tumors due to rare hereditary cancer syndromes.
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- Psycho-Oncology, 2011, v. 20, n. 6, p. 631, doi. 10.1002/pon.1951
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- Article
Li–Fraumeni Syndrome: Mutation of TP53 Is a Biomarker of Hereditary Predisposition to Tumor: New Insights and Advances in the Treatment.
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- Cancers, 2022, v. 14, n. 15, p. 3664, doi. 10.3390/cancers14153664
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- Article
Easing the Burden: Describing the Role of Social, Emotional and Spiritual Support in Research Families with Li-Fraumeni Syndrome.
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- Journal of Genetic Counseling, 2016, v. 25, n. 3, p. 529, doi. 10.1007/s10897-015-9905-x
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- Article
Li-Fraumeni syndrome with simultaneous osteosarcoma and liver cancer: Increased expression of a CD44 variant isoform after chemotherapy.
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- BMC Cancer, 2012, v. 12, n. 1, p. 444, doi. 10.1186/1471-2407-12-444
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- Article
Choroid Plexus Carcinomas With TP53 Germline Mutations: Management and Outcome.
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- Frontiers in Oncology, 2021, v. 11, p. 1, doi. 10.3389/fonc.2021.751784
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- Article
Pleomorphic dermal sarcoma presenting in a child with Li‐Fraumeni syndrome: A case report and review of the literature.
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- Pediatric Dermatology, 2024, v. 41, n. 2, p. 311, doi. 10.1111/pde.15452
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- Article
Apparently ' BRCA-Related' Breast and Ovarian Cancer Patient With Germline TP53 Mutation.
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- Breast Journal, 2011, v. 17, n. 4, p. 409, doi. 10.1111/j.1524-4741.2011.01088.x
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- Article
22. Li-Fraumeni Syndrome, including Li-Fraumeni-Like Syndrome.
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- JNCI: Journal of the National Cancer Institute, 2008, n. 38, p. 48
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- Article
Myelodysplastic Syndromes Arising in Patients With Germline TP53 Mutation and Li-Fraumeni Syndrome.
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- Archives of Pathology & Laboratory Medicine, 2010, v. 134, n. 7, p. 1010, doi. 10.5858/2009-0015-oa.1
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- Article
Cell-free DNA from germline TP53 mutation carriers reflect cancer-like fragmentation patterns.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-51529-w
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- Article
A Case of Synchronous Malignancy with Novel Missense Mutation in a Child: Is This Li-Fraumeni Syndrome or a Novel Case Masquerading as Li-Fraumeni Syndrome??
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- Indian Journal of Medical & Paediatric Oncology, 2020, v. 41, n. 5, p. 777, doi. 10.4103/ijmpo.ijmpo_202_20
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- Article
Prevalence of germline TP53 mutations in a prospective series of unselected patients with adrenocortical carcinoma.
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- 2013
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- journal article
Baseline surveillance in Li Fraumeni syndrome using whole-body MRI: a systematic review and updated meta-analysis.
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- European Radiology, 2025, v. 35, n. 2, p. 643, doi. 10.1007/s00330-024-10983-2
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- Article
Risks of first and subsequent cancers among TP53 mutation carriers in the National Cancer Institute Li-Fraumeni syndrome cohort.
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- 2016
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- journal article
Sarcomas in TP53 germline mutation carriers.
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- Cancer (0008543X), 2012, v. 118, n. 5, p. 1387, doi. 10.1002/cncr.26390
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- Article
Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-022-35727-y
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- Article
The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations.
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- Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 1, doi. 10.1186/1750-1172-9-63
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- Article
The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations.
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- 2014
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- journal article
Inhibiting the Priming for Cancer in Li-Fraumeni Syndrome.
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- Cancers, 2022, v. 14, n. 7, p. 1621, doi. 10.3390/cancers14071621
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- Article
Synchronous choroid plexus papilloma and Wilms tumor in a girl, disclosing a Li-Fraumeni syndrome.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-020-00158-7
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- Article
Germline TP53 mutations in BRCA1 and BRCA2 mutation-negative French Canadian breast cancer families.
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- Breast Cancer Research & Treatment, 2008, v. 108, n. 3, p. 399, doi. 10.1007/s10549-007-9608-6
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- Article
Clinical Characteristics and Chemosensitivity in Germline TP53 Pathogenic Variant Cases Identified by Cancer Genomic Testing.
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- Cancer Genomics & Proteomics (1109-6535), 2025, v. 22, n. 2, p. 354, doi. 10.21873/cgp.20506
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- Article
Síndrome de Li Fraumeni Cáncer familiar Comunicación de un caso y revisión de la literatura.
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- Acta Ortopédica Mexicana, 2007, v. 21, n. 2, p. 99
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- Article
What Should a Gynecologist Know about Li-Fraumeni Syndrome? Lessons from a Patient Undergoing Hysterectomy for Benign Indications.
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- 2018
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- Case Study
Germline TP53 Variants and Susceptibility to Osteosarcoma.
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- JNCI: Journal of the National Cancer Institute, 2015, v. 107, n. 7, p. 1, doi. 10.1093/jnci/djv101
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- Article
Germline TP53 variants and susceptibility to osteosarcoma.
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- 2015
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- journal article
Functional evaluation of germline TP53 variants identified in Brazilian families at-risk for Li–Fraumeni syndrome.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-67810-3
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- Article
Breast Cancer after Radiation Therapy in a Patient with Li-Fraumeni Syndrome: A Case Report.
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- 2022
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- Case Study
The need for dynamic methods for measuring cell cycle perturbations: a study in radiation-treated lymphoblastoid cell lines of varying p53 status.
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- Cell Proliferation, 1999, v. 32, n. 1, p. 15, doi. 10.1046/j.1365-2184.1999.3210015.x
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- Article
Increasing Evidence for the Association of Breast Implant-Associated Anaplastic Large Cell Lymphoma and Li Fraumeni Syndrome.
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- Case Reports in Genetics, 2019, p. 1, doi. 10.1155/2019/5647940
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- Article
CHEK2 1100delC is not a risk factor for male breast cancer population.
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- International Journal of Cancer, 2004, v. 108, n. 3, p. 475
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- Article
Arsenic trioxide extends survival of Li–Fraumeni syndrome mimicking mouse.
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- Cell Death & Disease, 2023, v. 14, n. 11, p. 1, doi. 10.1038/s41419-023-06281-2
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- Article
Evaluation of Patients and Families With Concern for Predispositions to Hematologic Malignancies Within the Hereditary Hematologic Malignancy Clinic (HHMC).
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- 2016
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- journal article
Potential Mechanisms for Cancer Resistance in Elephants and Comparative Cellular Response to DNA Damage in Humans.
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- 2015
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- journal article
"I need to know if I'm going to die young": Adolescent and young adult experiences of genetic testing for Li–Fraumeni syndrome.
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- Journal of Psychosocial Oncology, 2021, v. 39, n. 1, p. 54, doi. 10.1080/07347332.2020.1768199
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- Article
Couples coping with screening burden and diagnostic uncertainty in Li-Fraumeni syndrome: Connection versus independence.
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- Journal of Psychosocial Oncology, 2019, v. 37, n. 2, p. 178, doi. 10.1080/07347332.2018.1543376
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- Article
The Brazilian TP53 mutation (R337H) and sarcomas.
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- PLoS ONE, 2020, v. 15, n. 1, p. 1, doi. 10.1371/journal.pone.0227260
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- Article
Perivascular Epithelioid Cell-Family Tumors in Children, Adolescents, and Young Adults: Clinicopathologic Features in 70 Cases.
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- Archives of Pathology & Laboratory Medicine, 2024, v. 148, n. 11, p. e374, doi. 10.5858/arpa.2023-0552-OA
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- Article
Re-irradiation using proton therapy for radiation-induced secondary cancer with Li-Fraumeni syndrome: A case report and review of literature.
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- Journal of Cancer Research & Therapeutics, 2020, v. 16, n. 6, p. 1524, doi. 10.4103/jcrt.JCRT_449_19
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- Article
Re-irradiation using proton therapy for radiation-induced secondary cancer with Li-Fraumeni syndrome: A case report and review of literature.
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- 2020
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- journal article
A surveillance clinic for children and adolescents with, or at risk of, hereditary cancer predisposition syndromes.
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- 2021
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- Publication type:
- Letter
Pleomorphic carcinoma of the lung arising in a patient with Li-Fraumeni syndrome: Report of a case.
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- Surgery Today, 2011, v. 41, n. 6, p. 841, doi. 10.1007/s00595-010-4359-0
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- Article
TP53 germline mutations in the context of families with hereditary breast and ovarian cancer: a clinical challenge.
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- 2021
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- Publication type:
- journal article
LI-FRAUMENI SYNDROME - A GENETIC DISORDER PREDISPOSING TO MULTIPLE MALIGNANCIES: CASE REPORT.
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- Acta Marisiensis. Seria Medica, 2024, v. 70, p. 225
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- Article
Joint effects of germ-line TP53 mutation, MDM2 SNP309, and gender on cancer risk in family studies of Li-Fraumeni syndrome.
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- Human Genetics, 2011, v. 129, n. 6, p. 663, doi. 10.1007/s00439-011-0957-1
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- Article
Melanoma in patients with Li-Fraumeni syndrome (Review).
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- Experimental & Therapeutic Medicine, 2022, v. 23, n. 1, p. N.PAG
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- Article
Laparoscopic resection of liver PEComa associated with Li‑Fraumeni syndrome: A case report.
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- 2024
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- Publication type:
- Case Study
A solitary case of gliosarcoma an indication for TP53 mutation analysis: a non-concordant finding. Case report.
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- Romanian Neurosurgery, 2021, v. 35, n. 2, p. 210, doi. 10.33962/roneuro-2021-034
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- Article
Communicatively constructing resilience: Exploring family resilience in the experience of hereditary cancer.
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- Family Relations, 2025, v. 74, n. 1, p. 519, doi. 10.1111/fare.13097
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- Publication type:
- Article