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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1983 1
1988 1
1989 1
1992 1
1993 1
1994 1
1995 1
1996 4
1998 2
1999 3
2000 3
2002 5
2003 4
2004 5
2005 5
2006 3
2007 2
2008 2
2009 3
2010 4
2011 1
2012 2
2013 7
2014 8
2015 8
2016 6
2017 7
2018 10
2019 7
2020 5
2021 9
2022 9
2023 15
2024 4

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138 results

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Page 1
Lynch Syndrome-Associated Colorectal Cancer.
Sinicrope FA. Sinicrope FA. N Engl J Med. 2018 Aug 23;379(8):764-773. doi: 10.1056/NEJMcp1714533. N Engl J Med. 2018. PMID: 30134129 Review. No abstract available.
Pathology and genetics of hereditary colorectal cancer.
Ma H, Brosens LAA, Offerhaus GJA, Giardiello FM, de Leng WWJ, Montgomery EA. Ma H, et al. Pathology. 2018 Jan;50(1):49-59. doi: 10.1016/j.pathol.2017.09.004. Epub 2017 Nov 21. Pathology. 2018. PMID: 29169633 Review.
Colorectal cancer (CRC) accounts for over 8% of all deaths annually worldwide. Between 2 and 5% of all CRCs occur due to inherited syndromes, including Lynch syndrome, familial adenomatous polyposis, MUTYH-associated polyposis, Peutz-Jeghers syndrom …
Colorectal cancer (CRC) accounts for over 8% of all deaths annually worldwide. Between 2 and 5% of all CRCs occur due to inher …
Targeted Therapy for Colorectal Cancer.
Sakata S, Larson DW. Sakata S, et al. Surg Oncol Clin N Am. 2022 Apr;31(2):255-264. doi: 10.1016/j.soc.2021.11.006. Epub 2022 Mar 9. Surg Oncol Clin N Am. 2022. PMID: 35351276 Review.
Metastatic colorectal cancer (mCRC) is incurable in patients with unresectable disease. ...Finally, for the minority patients with microsatellite instability (MSI) high/mismatch repair (MMR) deficient tumors, either due to Lynch syndrome or sporadic mutations …
Metastatic colorectal cancer (mCRC) is incurable in patients with unresectable disease. ...Finally, for the minority patients with mi …
Familial adenomatous polyposis.
Half E, Bercovich D, Rozen P. Half E, et al. Orphanet J Rare Dis. 2009 Oct 12;4:22. doi: 10.1186/1750-1172-4-22. Orphanet J Rare Dis. 2009. PMID: 19822006 Free PMC article. Review.
Familial adenomatous polyposis (FAP) is characterized by the development of many tens to thousands of adenomas in the rectum and colon during the second decade of life. FAP has an incidence at birth of about 1/8,300, it manifests equally in both sexes, and accounts for les …
Familial adenomatous polyposis (FAP) is characterized by the development of many tens to thousands of adenomas in the rectum and colon durin …
Updated consensus guidelines on the management of Phelan-McDermid syndrome.
Srivastava S, Sahin M, Buxbaum JD, Berry-Kravis E, Soorya LV, Thurm A, Bernstein JA, Asante-Otoo A, Bennett WE Jr, Betancur C, Brickhouse TH, Passos Bueno MR, Chopra M, Christensen CK, Cully JL, Dies K, Friedman K, Gummere B, Holder JL Jr, Jimenez-Gomez A, Kerins CA, Khan O, Kohlenberg T, Lacro RV, Levi LA, Levy T, Linnehan D, Eva L, Moshiree B, Neumeyer A, Paul SM, Phelan K, Persico A, Rapaport R, Rogers C, Saland J, Sethuram S, Shapiro J, Tarr PI, White KM, Wickstrom J, Williams KM, Winrow D, Wishart B, Kolevzon A. Srivastava S, et al. Am J Med Genet A. 2023 Aug;191(8):2015-2044. doi: 10.1002/ajmg.a.63312. Epub 2023 Jul 1. Am J Med Genet A. 2023. PMID: 37392087 Review.
Phelan-McDermid syndrome (PMS) is a genetic condition caused by SHANK3 haploinsufficiency and characterized by a wide range of neurodevelopmental and systemic manifestations. ...
Phelan-McDermid syndrome (PMS) is a genetic condition caused by SHANK3 haploinsufficiency and characterized by a wide range of neurod …
Health equity in the implementation of genomics and precision medicine: A public health imperative.
Khoury MJ, Bowen S, Dotson WD, Drzymalla E, Green RF, Goldstein R, Kolor K, Liburd LC, Sperling LS, Bunnell R. Khoury MJ, et al. Genet Med. 2022 Aug;24(8):1630-1639. doi: 10.1016/j.gim.2022.04.009. Epub 2022 Apr 28. Genet Med. 2022. PMID: 35482015 Free PMC article. Review.
Studies have shown lower implementation rates for selected diseases with tier 1 applications (familial hypercholesterolemia, Lynch syndrome, hereditary breast and ovarian cancer) among racial and ethnic minority groups, rural communities, uninsured or underin …
Studies have shown lower implementation rates for selected diseases with tier 1 applications (familial hypercholesterolemia, Lynch …
AGA Clinical Practice Update on Pancreas Cancer Screening in High-Risk Individuals: Expert Review.
Aslanian HR, Lee JH, Canto MI. Aslanian HR, et al. Gastroenterology. 2020 Jul;159(1):358-362. doi: 10.1053/j.gastro.2020.03.088. Epub 2020 May 19. Gastroenterology. 2020. PMID: 32416142 Review.
BEST PRACTICE ADVICE 2: Pancreas cancer screening should be considered in patients with genetic syndromes associated with an increased risk of pancreas cancer, including all patients with Peutz-Jeghers syndrome, hereditary pancreatitis, patients with CDKN2A gene mut …
BEST PRACTICE ADVICE 2: Pancreas cancer screening should be considered in patients with genetic syndromes associated with an increased risk …
Inherited renal carcinomas.
Kawashima A, Young SW, Takahashi N, King BF, Atwell TD. Kawashima A, et al. Abdom Radiol (NY). 2016 Jun;41(6):1066-78. doi: 10.1007/s00261-016-0743-6. Abdom Radiol (NY). 2016. PMID: 27108134 Review.
Hereditary forms of kidney carcinoma account for 5-8% of all malignant kidney neoplasms. ...This manuscript reviews the clinical and imaging findings of well-defined inherited kidney cancer syndromes including von Hippel-Lindau disease, Birt-Hogg-Dube synd …
Hereditary forms of kidney carcinoma account for 5-8% of all malignant kidney neoplasms. ...This manuscript reviews the …
Review article: Lynch Syndrome-a mechanistic and clinical management update.
Curtius K, Gupta S, Boland CR. Curtius K, et al. Aliment Pharmacol Ther. 2022 Apr;55(8):960-977. doi: 10.1111/apt.16826. Epub 2022 Mar 21. Aliment Pharmacol Ther. 2022. PMID: 35315099 Free PMC article. Review.
BACKGROUND: Lynch syndrome (LS) is an autosomal dominant familial condition caused by a pathogenic variant (PV) in a DNA mismatch repair gene, which then predisposes carriers to various cancers. ...Individuals with LS have increased risks for colorectal, endo …
BACKGROUND: Lynch syndrome (LS) is an autosomal dominant familial condition caused by a pathogenic variant (PV) in a DNA misma …
Immunology of Lynch Syndrome.
Pastor DM, Schlom J. Pastor DM, et al. Curr Oncol Rep. 2021 Jun 14;23(8):96. doi: 10.1007/s11912-021-01085-z. Curr Oncol Rep. 2021. PMID: 34125344 Free PMC article. Review.
PURPOSE OF REVIEW: Patients with Lynch syndrome have a high probability of developing colorectal and other carcinomas. This review provides a comprehensive assessment of the immunologic aspects of Lynch syndrome pathogenesis and provides an over …
PURPOSE OF REVIEW: Patients with Lynch syndrome have a high probability of developing colorectal and other carcinomas. …
138 results