Results 1 to 10 of about 1,064,760 (292)

Morphological Analyses of Colorectal Adenocarcinomas in Japanese Familial Adenomatous Polyposis Patients

open access: yesJournal of the Anus, Rectum and Colon, 2022
Objectives: This retrospective study was conducted to clarify the morphological characteristics of colorectal cancer (CRC) in Japanese familial adenomatous polyposis (FAP) patients.
Yozo Suzuki   +11 more
doaj   +1 more source

A Comparison of Patient-Reported Outcomes Following Consent for Genetic Testing Using an Oncologist- or Genetic Counselor-Mediated Model of Care

open access: yesCurrent Oncology, 2021
This study compares knowledge, experience and understanding of genetic testing, and psychological outcomes among breast and ovarian cancer patients undergoing multi-gene panel testing via genetic counselor-mediated (GMT) or oncologist-mediated (OMT ...
Jeanna M. McCuaig   +5 more
doaj   +1 more source

Personalising genetic counselling (POETIC) trial: Protocol for a hybrid type II effectiveness-implementation randomised clinical trial of a patient screening tool to improve patient empowerment after cancer genetic counselling

open access: yesTrials, 2023
Background Genetic counselling aims to identify, and address, patient needs while facilitating informed decision-making about genetic testing and promoting empowerment and adaptation to genetic information.
Laura E. Forrest   +10 more
doaj   +1 more source

Comparison of Clinicopathological Characteristics Between Primary and Contralateral Cancers in BRCA1/2 Carriers with Metachronous Bilateral Breast Cancers

open access: yesZhongliu Fangzhi Yanjiu, 2023
Objective To compare the clinicopathological characteristics between primary and contralateral cancers in patients with metachronous bilateral breast cancer (MBBC) who carried a BRCA1/2 germline pathogenic variant. Methods A total of 496 BRCA1/2 carriers
DING Xinyun   +6 more
doaj   +1 more source

Cancer risk in relatives of BRCA1/2 pathogenic variant carriers in a large series of unselected patients with breast cancer

open access: yesCancer Biology & Medicine, 2023
Objective: The spectrum and risk of cancer in relatives of BRCA1/2 pathogenic variant carriers in the Chinese population have not been established. Methods: A family history of cancer in 9903 unselected breast cancer patients was retrospectively analyzed.
Jiaming Liu   +7 more
doaj   +1 more source

Migration, families, and counterfactual families

open access: yes, 2023
Migration changes how families form and dissolve, and how one should conceptualize the family. This has implications for thinking about how the migration decision is modelled when individuals are unable to picture the counterfactual families they may have.
Mckenzie, David   +2 more
openaire   +3 more sources

Clinical relevance of pathogenic germline variants in mismatch repair genes in Chinese breast cancer patients

open access: yesnpj Breast Cancer, 2022
The prevalence and clinical relevance of pathogenic germline variants in MMR genes have not been investigated in large series of breast cancers. In this study, we screened the germline variants in MMR genes in 8085 consecutive Chinese breast cancer ...
Li Hu   +13 more
doaj   +1 more source

Psychological and health behaviour outcomes following multi-gene panel testing for hereditary breast and ovarian cancer risk: a mini-review of the literature

open access: yesHereditary Cancer in Clinical Practice, 2022
Introduction Knowledge of the genetic mechanisms driving hereditary breast and ovarian cancer (HBOC) has recently expanded due to advances in gene sequencing technologies.
Lindsay Carlsson   +3 more
doaj   +1 more source

Current clinical practice for familial adenomatous polyposis in Japan: A nationwide multicenter study

open access: yesAnnals of Gastroenterological Surgery, 2022
Introduction In Japanese patients with familial adenomatous polyposis (FAP), colectomy tends to be postponed or avoided. Aim This study aimed to clarify the current clinical practice from a Japanese multicenter cohort study database.
Takaaki Matsubara   +13 more
doaj   +1 more source

Familial Hypercholesterolemia [PDF]

open access: yesCardiology Clinics, 2015
Familial hypercholesterolemia is a common, inherited disorder of cholesterol metabolism that leads to early cardiovascular morbidity and mortality. It is underdiagnosed and undertreated. Statins, ezetimibe, bile acid sequestrants, niacin, lomitapide, mipomersen, and low-density lipoprotein (LDL) apheresis are treatments that can lower LDL cholesterol ...
Victoria Enchia, Bouhairie   +1 more
openaire   +3 more sources

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