Works matching Lynch syndrome
Results: 2452
Molecular diagnosis of hereditary nonpolyposis colorectal cancer (Lynch syndrome).
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- Revista Facultad de Medicina de la Universidad Nacional de Colombia, 2016, v. 64, n. 3, p. 537, doi. 10.15446/revfacmed.v64n3.48458
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- Article
Lynch-like Syndrome: Potential Mechanisms and Management.
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- Cancers, 2022, v. 14, n. 5, p. 1115, doi. 10.3390/cancers14051115
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- Publication type:
- Article
Early-onset colorectal cancer patients without family history are "at very low risk" for lynch syndrome.
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- Journal of Experimental & Clinical Cancer Research (17569966), 2014, v. 33, n. 1, p. 1, doi. 10.1186/1756-9966-33-1
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- Article
Semiquantitative assessment of immunohistochemistry for mismatch repair proteins in Lynch syndrome.
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- Histopathology, 2010, v. 56, n. 3, p. 331, doi. 10.1111/j.1365-2559.2010.03485.x
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- Article
Lynch syndrome: clinical, pathological, and genetic insights.
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- Langenbeck's Archives of Surgery, 2012, v. 397, n. 4, p. 513, doi. 10.1007/s00423-012-0918-8
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- Article
Quality colonoscopy and risk of interval cancer in Lynch syndrome.
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- International Journal of Colorectal Disease, 2013, v. 28, n. 12, p. 1643, doi. 10.1007/s00384-013-1745-2
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- Article
Lynch syndrome in Tunisia: first description of clinical features and germline mutations.
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- International Journal of Colorectal Disease, 2011, v. 26, n. 4, p. 455, doi. 10.1007/s00384-010-1129-9
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- Article
Synchronous gynecologic malignancy and preliminary results of Lynch syndrome.
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- Journal of Gynecologic Oncology, 2011, v. 22, n. 4, p. 233, doi. 10.3802/jgo.2011.22.4.233
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- Article
Lynch syndrome in a 15-year-old boy.
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- 2008
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- journal article
Risk-reducing surgery in hereditary gynecological cancer: Clinical applications in Lynch syndrome and hereditary breast and ovarian cancer (Review).
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- Molecular & Clinical Oncology, 2015, v. 3, n. 2, p. 267, doi. 10.3892/mco.2014.460
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- Article
A review on the molecular diagnostics of Lynch syndrome: a central role for the pathology laboratory.
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- Journal of Cellular & Molecular Medicine, 2010, v. 14, n. 1/2, p. 181, doi. 10.1111/j.1582-4934.2009.00977.x
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- Article
Epigenetic mechanisms in the pathogenesis of Lynch syndrome.
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- Clinical Genetics, 2014, v. 85, n. 5, p. 403, doi. 10.1111/cge.12349
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- Article
First successful double-factor PGD for Lynch syndrome: monogenic analysis and comprehensive aneuploidy screening.
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- Clinical Genetics, 2013, v. 84, n. 1, p. 70, doi. 10.1111/cge.12025
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- Article
Changes in screening behaviors and attitudes toward screening from pre-test genetic counseling to post-disclosure in Lynch syndrome families.
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- Clinical Genetics, 2013, v. 83, n. 3, p. 215, doi. 10.1111/cge.12091
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- Article
Impact of colonoscopic screening in male and female Lynch syndrome carriers with an MSH2 mutation.
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- Clinical Genetics, 2012, v. 82, n. 5, p. 439, doi. 10.1111/j.1399-0004.2011.01802.x
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- Article
Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome.
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- Clinical Genetics, 2011, v. 79, n. 6, p. 512, doi. 10.1111/j.1399-0004.2010.01594.x
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- Article
<i>BRAF</i> mutation in sporadic colorectal cancer and Lynch syndrome.
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- Virchows Archiv: European Journal of Pathology, 2013, v. 463, n. 5, p. 613, doi. 10.1007/s00428-013-1470-9
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- Article
Interval colon cancer in a Lynch syndrome patient under annual colonoscopic surveillance: a case for advanced imaging techniques?
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- BMC Gastroenterology, 2012, v. 12, n. 1, p. 50, doi. 10.1186/1471-230X-12-50
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- Article
Knowledge, Attitudes and Referral Patterns of Lynch Syndrome: A Survey of Clinicians in Australia.
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- Journal of Personalized Medicine, 2014, v. 4, n. 2, p. 218, doi. 10.3390/jpm4020218
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- Article
Barriers and Motivators for Referral of Patients with Suspected Lynch Syndrome to Cancer Genetic Services: A Qualitative Study.
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- Journal of Personalized Medicine, 2014, v. 4, n. 1, p. 20, doi. 10.3390/jpm4010020
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- Article
Genetic Testing for Lynch Syndrome, an Inherited Cancer of the Bowel, Endometrium, and Ovary.
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- Reviews in Obstetrics & Gynecology, 2012, v. 5, n. 1, p. 42, doi. 10.3909/riog0187
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- Article
Colorectal Neoplasia Detection Rates in Lynch Syndrome.
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- Cancers, 2024, v. 16, n. 23, p. 4021, doi. 10.3390/cancers16234021
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- Article
Real-World Data on Institutional Implementation of Screening for Mismatch Repair Deficiency and Lynch Syndrome in Endometrial Cancer Patients.
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- Cancers, 2024, v. 16, n. 3, p. 671, doi. 10.3390/cancers16030671
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- Article
Whole-Exome Sequencing Identifies Pathogenic Germline Variants in Patients with Lynch-Like Syndrome.
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- Cancers, 2022, v. 14, n. 17, p. 4233, doi. 10.3390/cancers14174233
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- Article
Detection of Microsatellite Instability in Colonoscopic Biopsies and Postal Urine Samples from Lynch Syndrome Cancer Patients Using a Multiplex PCR Assay.
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- Cancers, 2022, v. 14, n. 15, p. 3838, doi. 10.3390/cancers14153838
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- Article
Upper Gastrointestinal Cancer Surveillance in Lynch Syndrome.
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- Cancers, 2022, v. 14, n. 4, p. 1000, doi. 10.3390/cancers14041000
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- Article
Identification of Lynch Syndrome Carriers among Patients with Small Bowel Adenocarcinoma.
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- Cancers, 2021, v. 13, n. 24, p. 6378, doi. 10.3390/cancers13246378
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- Article
Partial duplication of MSH2 spanning exons 7 through 14 in Lynch syndrome.
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- Journal of Gastroenterology, 2013, v. 48, n. 6, p. 770, doi. 10.1007/s00535-013-0804-3
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- Article
Mismatch repair gene mutation analysis and colonoscopy surveillance in Chinese lynch syndrome families.
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- Cellular Oncology (2211-3428), 2013, v. 36, n. 3, p. 225, doi. 10.1007/s13402-013-0130-z
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- Article
Patient-reported disease knowledge and educational needs in Lynch syndrome: findings of an interactive multidisciplinary patient conference.
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- 2014
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- Publication type:
- Proceeding
Germline deletions in the EPCAM gene as a cause of Lynch syndrome - literature review.
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- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-9
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- Article
Mutation spectrum in South American Lynch syndrome families.
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- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-18
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- Article
Risk assessment and genetic counseling for Lynch syndrome – Practice resource of the National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer.
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- Journal of Genetic Counseling, 2022, v. 31, n. 3, p. 568, doi. 10.1002/jgc4.1546
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- Article
Genetic counselors' perspectives on population‐based screening for BRCA‐related hereditary breast and ovarian cancer and Lynch syndrome.
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- Journal of Genetic Counseling, 2021, v. 30, n. 1, p. 158, doi. 10.1002/jgc4.1305
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- Article
Preferences for outcomes associated with decisions to undergo or forgo genetic testing for Lynch syndrome.
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- Cancer (0008543X), 2013, v. 119, n. 1, p. 215, doi. 10.1002/cncr.27634
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- Article
BRAF V600E Mutation Analysis Simplifies the Testing Algorithm for Lynch Syndrome.
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- American Journal of Clinical Pathology, 2013, v. 140, n. 2, p. 177, doi. 10.1309/AJCPB9FOVH1HGKFR
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- Article
Bleeding Mass in Remnant Stomach, Unveiling Lynch Syndrome 18 Years After Bariatric Roux-En-Y Gastric Bypass Surgery.
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- ACG Case Reports Journal, 2024, v. 11, n. 4, p. 1, doi. 10.14309/crj.0000000000001323
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- Article
Primary Sclerosing Epithelioid Fibrosarcoma of the Lung in a Patient with Lynch Syndrome.
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- 2012
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- Report
Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients.
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- BMC Medical Genomics, 2013, v. 6, n. 1, p. 1, doi. 10.1186/1755-8794-6-10
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- Article
Performance of clinical guidelines compared with molecular tumour screening methods in identifying possible Lynch syndrome among colorectal cancer patients: a Norwegian population-based study.
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- 2010
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- Publication type:
- journal article
Ureteroscopic management of upper tract urothelial carcinoma ( UTUC) in patients with Lynch Syndrome (hereditary nonpolyposis colorectal cancer syndrome).
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- BJU International, 2013, v. 112, n. 6, p. 813, doi. 10.1111/bju.12008
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- Publication type:
- Article
Clinical and Molecular Assessment of Patients with Lynch Syndrome and Sarcomas Underpinning the Association with MSH2 Germline Pathogenic Variants.
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- Cancers, 2020, v. 12, n. 7, p. 1848, doi. 10.3390/cancers12071848
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- Publication type:
- Article
Tumour-specific methylation of PTPRG intron 1 locus in sporadic and Lynch syndrome colorectal cancer.
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- European Journal of Human Genetics, 2011, v. 19, n. 3, p. 307, doi. 10.1038/ejhg.2010.187
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- Article
Prophylactic surgery in Lynch syndrome.
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- Techniques in Coloproctology, 2011, v. 15, n. 2, p. 129, doi. 10.1007/s10151-010-0666-0
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- Publication type:
- Article
A Meta-Analysis of Obesity and Risk of Colorectal Cancer in Patients with Lynch Syndrome: The Impact of Sex and Genetics.
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- Nutrients, 2021, v. 13, n. 5, p. 1736, doi. 10.3390/nu13051736
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- Article
The MSH2 c.388_389del mutation shows a founder effect in Portuguese Lynch syndrome families.
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- Clinical Genetics, 2013, v. 84, n. 3, p. 244, doi. 10.1111/cge.12062
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- Publication type:
- Article
Impact of gynecological screening in Lynch syndrome carriers with an MSH2 mutation.
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- Clinical Genetics, 2013, v. 83, n. 4, p. 359, doi. 10.1111/j.1399-0004.2012.01929.x
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- Publication type:
- Article
Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts.
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- Journal of Gastroenterology & Hepatology, 2017, v. 32, n. 2, p. 427, doi. 10.1111/jgh.13468
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- Article
Identification of Lynch Syndrome in Patients with Endometrial Cancer Based on a Germline Next Generation Sequencing Multigene Panel Test.
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- Cancers, 2022, v. 14, n. 14, p. N.PAG, doi. 10.3390/cancers14143406
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- Publication type:
- Article
Patterns of germline and somatic testing after universal tumor screening for Lynch syndrome: A clinical practice survey of active members of the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer.
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- Journal of Genetic Counseling, 2022, v. 31, n. 4, p. 949, doi. 10.1002/jgc4.1567
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- Publication type:
- Article