Development of an integrated support system for hereditary cancer and its impact on gynecologic services. (Q43749121)

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3 March 2020

title

Development of an integrated support system for hereditary cancer and its impact on gynecologic services (English)

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3 March 2020

9

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3 March 2020

author name string

Mina Morii-Kashima

1

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3 March 2020

Hiroshi Tsubamoto

2

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3 March 2020

Chika Sato

3

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3 March 2020

Mariko Ushioda

4

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3 March 2020

Naohiro Tomita

5

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3 March 2020

Yasuo Miyoshi

6

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3 March 2020

Tomoko Hashimoto-Tamaoki

7

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3 March 2020

Kazuo Tamura

8

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3 March 2020

Hiroaki Shibahara

10

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3 March 2020

publication date

19 December 2013

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International Journal of Clinical Oncology

3 March 2020

published in

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3 March 2020

volume

19

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3 March 2020

issue

6

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3 March 2020

page(s)

1043-1051

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BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases

3 March 2020

cites work

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Hereditary gynecologic cancers: differential diagnosis, surveillance, management and surgical prophylaxis

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Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population.

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The prevalence of hereditary breast/ovarian cancer risk in patients with a history of breast or ovarian cancer in Japanese subjects

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Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels

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Focusing on patient needs and preferences may improve genetic counseling for colorectal cancer

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Risk factors for young premenopausal women with endometrial cancer

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Fertility preservation for patients with cancer: American Society of Clinical Oncology clinical practice guideline update

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Hereditary breast and ovarian cancer (HBOC): clinical features and counseling for BRCA1 and BRCA2, Lynch syndrome, Cowden syndrome, and Li-Fraumeni syndrome

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Does this patient have a family history of cancer? An evidence-based analysis of the accuracy of family cancer history

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Confirmation of Family Cancer History Reported in a Population-Based Survey

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A self-administered family history questionnaire improves identification of women who warrant referral to genetic counseling for hereditary cancer risk

21 January 2018

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Results of annual screening in phase I of the United Kingdom familial ovarian cancer screening study highlight the need for strict adherence to screening schedule

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Current and emerging trends in Lynch syndrome identification in women with endometrial cancer.

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Clinicopathologic significance of DNA mismatch repair protein defects and endometrial cancer in women 40years of age and younger

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Women 50 years or younger with endometrial cancer: the argument for universal mismatch repair screening and potential for targeted therapeutics

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Improved survival with an intact DNA mismatch repair system in endometrial cancer

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A systematic review of gynecological cancer surveillance in women belonging to hereditary nonpolyposis colorectal cancer (Lynch syndrome) families

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Ovarian carcinoma in situ of presumable fallopian tube origin in a patient with Lynch syndrome: A case report

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Preferences for outcomes associated with decisions to undergo or forgo genetic testing for Lynch syndrome

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Mortality after bilateral salpingo-oophorectomy in BRCA1 and BRCA2 mutation carriers: a prospective cohort study

21 January 2018

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Effect of prevention strategies on survival and quality-adjusted survival of women with BRCA1/2 mutations: an updated decision analysis

21 January 2018

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Significant differences among physician specialties in management recommendations of BRCA1 mutation carriers

21 January 2018

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Keeping it simple: genetics referrals for all invasive serous ovarian cancers

21 January 2018

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What women with ovarian cancer think and know about genetic testing

21 January 2018

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Endometrial cancer patients and compliance with genetic counseling: room for improvement

21 January 2018

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Society of Gynecologic Oncologists Education Committee Statement on Risk Assessment for Inherited Gynecologic Cancer Predispositions☆

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How Should Women With Early-Onset Endometrial Cancer Be Evaluated for Lynch Syndrome?

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Colonic late-onset familial adenomatous polyposis combined with severe duodenal polyposis and familial endometrial cancer

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Relationship of lower uterine segment cancer with Lynch syndrome: a novel case with an hMLH1 germline mutation

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Using a Plan‐Do‐Study‐Act Cycle to Introduce a New OR Service Line

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Prophylactic Surgery to Reduce the Risk of Gynecologic Cancers in the Lynch Syndrome

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