Consequences of universal MSI/IHC in screening ENDOMETRIAL cancer patients for Lynch syndrome. - Wikidata - awgldk - TriplyDB

Consequences of universal MSI/IHC in screening ENDOMETRIAL cancer patients for Lynch syndrome.

Consequences of universal MSI/IHC in screening ENDOMETRIAL cancer patients for Lynch syndrome.

http://www.wikidata.org/entity/Q34017044

about

Clinical Challenges Associated with Universal Screening for Lynch Syndrome-Associated Endometrial Cancer.Addressing the Role of Obesity in Endometrial Cancer Risk, Prevention, and Treatment.Impact of an immunohistochemistry-based universal screening protocol for Lynch syndrome in endometrial cancer on genetic counseling and testing.Cancer Survivorship Care: An Opportunity to Revisit Cancer Genetics.Reflex test reminders in required cancer synoptic templates decrease order entry error: An analysis of mismatch repair immunohistochemical orders to screen for Lynch syndrome.Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines.Lynch syndrome: five unanswered questions.Update on pathology, staging and molecular pathology of endometrial (uterine corpus) adenocarcinoma.Genetic screening for gynecological cancer: where are we heading?Finding the needle in a haystack: identification of cases of Lynch syndrome with MLH1 epimutation.Mismatch repair deficiency testing in clinical practice.Sociodemographic, psychosocial and clinical factors associated with uptake of genetic counselling for hereditary cancer: a systematic review.Prevalence of Lynch syndrome in unselected patients with endometrial or ovarian cancer.Importance of PCR-based Tumor Testing in the Evaluation of Lynch Syndrome-associated Endometrial Cancer.Evaluation of universal immunohistochemical screening of sebaceous neoplasms in a service setting.Improving attendance to genetic counselling services for gynaecological oncology patients.Targeted Screening With Combined Age- and Morphology-Based Criteria Enriches Detection of Lynch Syndrome in Endometrial Cancer.Genetic testing for Lynch syndrome in the province of Ontario.The prevalence of Lynch syndrome in women with endometrial cancer: a systematic review protocol

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P2860

Consequences of universal MSI/IHC in screening ENDOMETRIAL cancer patients for Lynch syndrome.

http://www.wikidata.org/entity/Q34017044

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2014 nî lūn-bûn

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2014 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2014 թվականի հունիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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Consequences of universal MSI/ ...... r patients for Lynch syndrome.

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Consequences of universal MSI/ ...... r patients for Lynch syndrome.

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Consequences of universal MSI/ ...... r patients for Lynch syndrome.

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Consequences of universal MSI/ ...... r patients for Lynch syndrome.

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Consequences of universal MSI/ ...... r patients for Lynch syndrome.

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Consequences of universal MSI/ ...... r patients for Lynch syndrome.

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Consequences of universal MSI/ ...... r patients for Lynch syndrome.

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Consequences of universal MSI/ ...... r patients for Lynch syndrome.

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Consequences of universal MSI/ ...... r patients for Lynch syndrome.

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P356

J.YGYNO.2014.06.009

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Gynecologic Oncology

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Consequences of universal MSI/ ...... r patients for Lynch syndrome.

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Amanda S Bruegl

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Bojana Djordjevic

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Brittany A L Batte

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Bryan M Fellman

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Karen H Lu

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Kari L Ring

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Katherine M Dempsey

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Rajyalakshmi Luthra

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Russell R Broaddus

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P2860

The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations

Outcomes of screening endometrial cancer patients for Lynch syndrome by patient-administered checklist

Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing.

Molecular characterization of MSI-H colorectal cancer by MLHI promoter methylation, immunohistochemistry, and mismatch repair germline mutation screening

Carcinoma of the lower uterine segment: a newly described association with Lynch syndrome.

Prevalence of Lynch syndrome among patients with newly diagnosed endometrial cancers.

Underutilization of Lynch syndrome screening in a multisite study of patients with colorectal cancer.

Reflex testing for Lynch syndrome: if we build it, will they come? Lessons learned from the uptake of clinical genetics services by individuals with newly diagnosed colorectal cancer (CRC).

Colorectal cancer survivors undergoing genetic testing for hereditary non-polyposis colorectal cancer: motivational factors and psychosocial functioning.

Somatic mutations in MLH1 and MSH2 are a frequent cause of mismatch-repair deficiency in Lynch syndrome-like tumors.

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319-325

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10.1016/J.YGYNO.2014.06.009

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2

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Molly S. Daniels

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2014-06-14T00:00:00Z

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