Cargando…

Use of Cytology to Diagnose Inherited Breast Cancer

Detalles Bibliográficos
Autores principales:	Møller, Pål, Evans, Gareth, Anderson, Elaine, Mæhle, Lovise, Lalloo, Fiona, Heimdal, Ketil R., Steel, C. Michael, The Biomed 2 Demonstration Programme on Inherited Breast Cancer
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	IOS Press 1999
Materias:	Abstract
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850806/ http://dx.doi.org/10.1155/1999/909834

Ejemplares similares

Mutation-Specific Survival of Inherited Breast Cancer
por: Møller, P., et al.
Publicado: (1999)

Costs and Benefits of Diagnosing Familial Breast Cancer
por: Heimdal, Ketil, et al.
Publicado: (1999)

Efficacy of Early Diagnosis and Treatment in Women with a Family History of Breast Cancer
por: Møller, Pål, et al.
Publicado: (1999)

BRCA1 1675delA and 1135insA Account for One Third of Norwegian Familial Breast-Ovarian Cancer and Are Associated with Later Disease Onset than Less Frequent Mutations
por: Borg, Åke, et al.
Publicado: (1999)

Germline PTEN mutations are rare and highly penetrant
por: Rustad, Cecilie F, et al.
Publicado: (2006)

BRCA1 and BRCA2 mutation spectrum – an update on mutation distribution in a large cancer genetics clinic in Norway
por: Heramb, Cecilie, et al.
Publicado: (2018)

Guidelines for Follow-Up of Women at High Risk for Inherited Breast Cancer: Consensus Statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer
por: Møller, P., et al.
Publicado: (1999)

No Sib Pair Concordance for Breast or Ovarian Cancer in BRCA1 Mutation Carriers
por: Møller, Pål, et al.
Publicado: (2007)

Inherited Cancer Genetic Epidemiology to Improve Precision Medicine
por: Møller, Pål, et al.
Publicado: (2022)

Survival in Norwegian BRCA1 mutation carriers with breast cancer
por: Hagen, Anne Irene, et al.
Publicado: (2009)

Ten modifiers of BRCA1 penetrance validated in a Norwegian series
por: Heramb, Cecilie, et al.
Publicado: (2015)

Relevance of breast cancer hormone receptors and other factors to the efficacy of adjuvant tamoxifen: patient-level meta-analysis of randomised trials
por: Early Breast Cancer Trialists' Collaborative Group (EBCTCG)
Publicado: (2011)

Comparisons between different polychemotherapy regimens for early breast cancer: meta-analyses of long-term outcome among 100 000 women in 123 randomised trials
por: Early Breast Cancer Trialists' Collaborative Group (EBCTCG)
Publicado: (2012)

Effect of radiotherapy after mastectomy and axillary surgery on 10-year recurrence and 20-year breast cancer mortality: meta-analysis of individual patient data for 8135 women in 22 randomised trials
por: EBCTCG (Early Breast Cancer Trialists' Collaborative Group)
Publicado: (2014)

The clinical utility of genetic testing in breast cancer kindreds: a prospective study in families without a demonstrable BRCA mutation
por: Møller, Pål, et al.
Publicado: (2014)

Uptake of Genetic Testing and Pre-Test Levels of Mental Distress in Norwegian Families with Known BRCA1 Mutations
por: Reichelt, Jon G., et al.
Publicado: (1999)

Uptake of genetic counseling, genetic testing and surveillance in hereditary malignant melanoma (CDKN2A) in Norway
por: Levin, Trine, et al.
Publicado: (2016)

High penetrances of BRCA1 and BRCA2 mutations confirmed in a prospective series
por: Møller, Pål, et al.
Publicado: (2010)

Current Policies for Surveillance and Management in Women at Risk for Breast and Ovarian Cancer: A Survey among 16 European Family Cancer Clinics
por: Vasen, H. F. A., et al.
Publicado: (1999)

The Norwegian PMS2 founder mutation c.989-1G > T shows high penetrance of microsatellite instable cancers with normal immunohistochemistry
por: Grindedal, Eli Marie, et al.
Publicado: (2014)

Germline FFPE inherited cancer panel testing in deceased family members: implications for clinical management of unaffected relatives
por: Bennett, Sarah, et al.
Publicado: (2021)

Differences in Management of Older Women Influence Breast Cancer Survival: Results from a Population-Based Database in Sweden
por: Eaker, Sonja, et al.
Publicado: (2006)

The pathology of familial breast cancer: Clinical and genetic counselling implications of breast cancer pathology
por: Lalloo, Fiona, et al.
Publicado: (1999)

Towards Evidence-Based Management of Inherited Breast and Breast-Ovarian Cancer
por: Møller, Pål
Publicado: (2004)

Diagnostic mRNA splicing assay for variants in BRCA1 and BRCA2 identified two novel pathogenic splicing aberrations
por: Wangensteen, Teresia, et al.
Publicado: (2019)

Biopsy or cytology for diagnosing hepatic focal lesions?
por: Kim, Haeryoung
Publicado: (2021)

Surgical Site Cytology to Diagnose Spinal Lesions
por: Koepke, Leon-Gordian, et al.
Publicado: (2022)

Diagnosing Czech Patients with Inherited Platelet Disorders
por: Louzil, Jan, et al.
Publicado: (2022)

Cytological Features of a Metastatic Angiosarcoma in the Lymph Node Diagnosed via Liquid-Based Cytology
por: Jhuang, Jie-Yang, et al.
Publicado: (2023)

Top Information Need Priorities of Older Adults Newly Diagnosed With Active Myeloma
por: Tariman1, Joseph D., et al.
Publicado: (2015)

Contemporary Management of Hodgkin Lymphoma and Chronic Lymphocytic Leukemia
por: Kurtin, Sandra E., et al.
Publicado: (2018)

Filariasis of the breast, diagnosed by fine needle aspiration cytology
por: Singh, Naorem G., et al.
Publicado: (2009)

Plasmacytoma of tonsil diagnosed by fine-needle aspiration cytology
por: Bhat, Ramachandra V, et al.
Publicado: (2010)

Incisional Endometriosis: Diagnosed by Fine Needle Aspiration Cytology
por: Veda, P, et al.
Publicado: (2010)

Primary hydatid cyst of the neck diagnosed by aspiration cytology
por: Chakrabarti, Indranil, et al.
Publicado: (2012)

Lymphangioleiomyomatosis diagnosed by effusion cytology: A case report
por: Rivera, Glorimar, et al.
Publicado: (2015)

Breast ductal carcinoma with coexistent microfilaria: Diagnosed on cytology
por: Mohan, Nitesh, et al.
Publicado: (2018)

Leptomeningeal Carcinomatosis Secondary to Esophageal Cancer Diagnosed on Cytology
por: Jagtap, Sunil Vitthalrao, et al.
Publicado: (2020)

Malignant peripheral nerve sheath tumours in inherited disease
por: Evans, D Gareth R, et al.
Publicado: (2012)

A Dominantly Inherited 5′ UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian Cancer
por: Evans, D.Gareth R., et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_ea2diajg42n1nreetph4bfqgka