Cargando…

An audit of families with unreported or misreported cancers verified through a population-based cancer registry: implications for providing cancer risk assessment and management advice by a Familial Cancer Centre

Detalles Bibliográficos
Autores principales:	Kentwell, M, Bogwitz, M, Donoghue, L, McArdle, T
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2012
Materias:	Meeting Abstract
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3326755/ http://dx.doi.org/10.1186/1897-4287-10-S2-A42

Ejemplares similares

Peer live supervision in the familial cancer setting
por: Kentwell, M, et al.
Publicado: (2012)

Improving the provision of Melbourne Health Familial Cancer services to Victoria’s Culturally and Linguistically Diverse (CALD) communities
por: Bylstra, Y, et al.
Publicado: (2012)

Misreported Cancer Deaths in PLATO Trial
por: Serebruany, Victor, et al.
Publicado: (2021)

Audit of routine immunohistochemistry testing for mismatch repair proteins at diagnosis of colorectal cancer under the age of 50
por: Lipton, L, et al.
Publicado: (2012)

An audit of treatment focussed BRCA1/2 mutation testing at an integrated Familial Cancer Clinic
por: Lewis, A, et al.
Publicado: (2012)

Use of unit standard paragraphs and letters in: 1. Australian Familial Cancer Centres 2. One Centre’s experience at Southern Health
por: Smyth, C, et al.
Publicado: (2012)

Misreporting of Energy Intake in the 2007 Australian Children’s Survey: Identification, Characteristics and Impact of Misreporters
por: Rangan, Anna M., et al.
Publicado: (2011)

Cancer predisposing BARD1 mutations in breast-ovarian cancer families
por: Ratajska, Magdalena, et al.
Publicado: (2012)

Comparing the quality of uniportal and multiportal video-assisted anatomical resection for primary lung cancer: the preliminary results of a single centre audit
por: Surendrakumar, Veena, et al.
Publicado: (2015)

Acknowledging unreported problems with active surveillance for prostate cancer: a prospective single-centre observational study
por: Hefermehl, Lukas J, et al.
Publicado: (2016)

Familial risk and diagnosis of colorectal cancer in young individuals
por: Elsakov, Pavel
Publicado: (2015)

"It's not even about her it's about the whole family": accounts of participation in a family cancer study
por: Shipman, H, et al.
Publicado: (2012)

Design considerations for massively parallel sequencing studies of common familial cancers
por: Feng, BJ, et al.
Publicado: (2012)

THE FAMILY SYNDROME OF SARCOMA, BREAST CANCER, AND OTHER NEOPLASMS: MEETING REPORT
por: Miller, Robert W., et al.
Publicado: (1988)

Audit of inpatient smoking cessation advice
por: Mohamed, Flensham, et al.
Publicado: (2021)

Reporting and misreporting of sex differences in the biological sciences
por: Garcia-Sifuentes, Yesenia, et al.
Publicado: (2021)

Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients
por: Thompson, ER, et al.
Publicado: (2012)

A breast cancer prediction model incorporating familial and personal risk factors
por: Cuzick, Jack
Publicado: (2012)

A genetic journey through cancer: from rarity and family to aspirin and nanowires
por: Burn, J
Publicado: (2012)

BRCA1 mutation analysis in breast and ovarian cancer families from Greece
por: Konstantopoulou, I, et al.
Publicado: (2000)

Estrogen receptor transcription and transactivation: ErbB family of receptors in breast cancer
por: Hynes, NE, et al.
Publicado: (2001)

The spectrum of mutations in families with breast and ovarian cancer from the region of Saxony, Germany
por: Tomys, Michalina, et al.
Publicado: (2015)

Audit of a radiographer/nurse-led family history breast cancer clinic
por: Willson, SA, et al.
Publicado: (2008)

PB.44: Audit of interval cancers from family history breast screening
por: Dunn, R, et al.
Publicado: (2013)

kConFab: a unique Australasian research initiative for familial breast cancer
por: Sambrook, J
Publicado: (2000)

Misreporting of contraceptive hormone use in clinical research participants
por: Achilles, Sharon L., et al.
Publicado: (2018)

An audit of primary surgical treatment for women with ovarian cancer referred to a cancer centre
por: Sengupta, P S, et al.
Publicado: (1999)

Screening and verifying the mutations in the LDLR and APOB genes in a Chinese family with familial hypercholesterolemia
por: Lv, Xian, et al.
Publicado: (2023)

Enhancing Cancer Control Through a Population-Based Cancer Registry in Cali, Colombia: Results From 20-Year Cancer Survival Trends
por: García, Luz Stella, et al.
Publicado: (2022)

Prospective surveillance of women with a family history of breast cancer: auditing the risk threshold
por: Anderson, E, et al.
Publicado: (2008)

Making a good model better - evaluation of the NSW Combined Family Cancer Clinic meetings
por: Purser, Lynne, et al.
Publicado: (2012)

Mutation detection in familial and sporadic breast cancers by denaturing high-performance liquid chromatography (DHPLC)
por: Betz, B, et al.
Publicado: (2001)

Constitutional alterations of 9p23-24 in independent BRCA2 breast cancer families
por: Schwab, M, et al.
Publicado: (2000)

Results of the IROCA international clinical audit in prostate cancer radiotherapy at six comprehensive cancer centres
por: Lopes de Castro, Carla, et al.
Publicado: (2021)

Recurrent N209* ABHD5 mutation in two unreported families with Chanarin Dorfman Syndrome
por: Tavian, Daniela, et al.
Publicado: (2021)

The impact of young age on cancer-specific and non-cancer-related survival after surgery for colorectal cancer: 10-year follow-up
por: McMillan, D C, et al.
Publicado: (2009)

Disclosing genetic research results: experiences of the Colon Cancer Family Registry
por: Keogh, Louise, et al.
Publicado: (2011)

Genetic Variations in SMAD7 Are Associated with Colorectal Cancer Risk in the Colon Cancer Family Registry
por: Jiang, Xuejuan, et al.
Publicado: (2013)

Targeted sequencing of established and candidate colorectal cancer genes in the Colon Cancer Family Registry Cohort
por: Raskin, Leon, et al.
Publicado: (2017)

Large genomic rearrangements in BRCA1 and BRCA2 genes in breast and ovarian cancer families in Poland
por: Bielecka, Helena, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_lodg8fki8b11lss2koht35jamg