Lynch syndrome [NEW TOPIC PAGE]

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From PubMed Clinical Queries

PubMed Clinical Queries is an utility offered by PubMed to search scientific literature in specific clinical research areas

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• Search PubMed Clinical Queries for "Lynch syndrome" 

Results: 5 of 601

• Update on the role of chromoendoscopy in colonoscopic surveillance of patients with Lynch syndrome.
  van de Wetering AJP, Bogie RMM, Cabbolet ACOG, Winkens B, Masclee AAM, Sanduleanu S.Eur J Gastroenterol Hepatol. 2018 Jul 23; . Epub 2018 Jul 23.
• Efficient Detection of Copy Number Mutations in PMS2 Exons with a Close Homolog.
  Herman DS, Smith C, Liu C, Vaughn CP, Palaniappan S, Pritchard CC, Shirts BH.J Mol Diagn. 2018 Jul; 20(4):512-521. Epub 2018 May 22.
• [Molecular Targeted Therapies for Hereditary Cancer Syndrome].
  Shimodaira H.Gan To Kagaku Ryoho. 2018 Apr; 45(4):587-592.
• Alcohol consumption and early-onset risk of colorectal cancer in Japanese patients with Lynch syndrome: a cross-sectional study conducted by the Japanese Society for Cancer of the Colon and Rectum.
  Miguchi M, Hinoi T, Tanakaya K, Yamaguchi T, Furukawa Y, Yoshida T, Tamura K, Sugano K, Ishioka C, Matsubara N, et al.Surg Today. 2018 Aug; 48(8):810-814. Epub 2018 Mar 24.
• Double somatic mutations in mismatch repair genes are frequent in colorectal cancer after Hodgkin's lymphoma treatment.
  Rigter LS, Snaebjornsson P, Rosenberg EH, Atmodimedjo PN, Aleman BM, Ten Hoeve J, Geurts-Giele WR, PALGA group., van Ravesteyn TW, Hoeksel J, et al.Gut. 2018 Mar; 67(3):447-455. Epub 2016 Nov 8.

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This column displays citations filtered to a specific clinical study category and scope. These search filters were developed by Haynes RB et al. See more filter information.

Systematic Reviews

Results: 5 of 151

• Update on the role of chromoendoscopy in colonoscopic surveillance of patients with Lynch syndrome.
  van de Wetering AJP, Bogie RMM, Cabbolet ACOG, Winkens B, Masclee AAM, Sanduleanu S.Eur J Gastroenterol Hepatol. 2018 Jul 23; . Epub 2018 Jul 23.
• The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice.
  Menko FH, Ter Stege JA, van der Kolk LE, Jeanson KN, Schats W, Moha DA, Bleiker EMA.Fam Cancer. 2018 May 30; . Epub 2018 May 30.
• Left-Sided Dominance of Early-Onset Colorectal Cancers: A Rationale for Screening Flexible Sigmoidoscopy in the Young.
  Segev L, Kalady MF, Church JM.Dis Colon Rectum. 2018 Aug; 61(8):897-902.
• Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP.
  Van Dijck A, Vulto-van Silfhout AT, Cappuyns E, van der Werf IM, Mancini GM, Tzschach A, Bernier R, Gozes I, Eichler EE, Romano C, et al.Biol Psychiatry. 2018 Mar 15; . Epub 2018 Mar 15.
• Hereditary Cancers in Gynecology: What Physicians Should Know About Genetic Testing, Screening, and Risk Reduction.
  Ring KL, Modesitt SC.Obstet Gynecol Clin North Am. 2018 Mar; 45(1):155-173.

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This column displays citations for systematic reviews, meta-analyses, reviews of clinical trials, evidence-based medicine, consensus development conferences, and guidelines. See filter information or additional related sources.

Medical Genetics

Topic:AllDiagnosisDifferential DiagnosisClinical DescriptionManagementGenetic CounselingMolecular GeneticsGenetic Testing

Results: 5 of 5021

• Routine molecular analysis for Lynch syndrome among adenomas or colorectal cancer within a national screening program.
  Goverde A, Wagner A, Bruno MJ, Hofstra RMW, Doukas M, van der Weiden MM, Dubbink HJ, Dinjens WNM, Spaander MCW.Gastroenterology. 2018 Jul 28; . Epub 2018 Jul 28.
• No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies.
  Engel C, Vasen HF, Seppälä T, Aretz S, Bigirwamungu-Bargeman M, de Boer SY, Bucksch K, Büttner R, Feder EH, Holzapfel S, et al.Gastroenterology. 2018 Jul 28; . Epub 2018 Jul 28.
• The First Molecular Screening of MLH1 and MSH2 Genes in Moroccan Colorectal Cancer Patients Shows a Relatively High Mutational Prevalence.
  Moufid FZ, Bouguenouch L, El Bouchikhi I, Chbani L, Iraqui Houssaini M, Sekal M, Belhassan K, Bennani B, Ouldim K.Genet Test Mol Biomarkers. 2018 Jul 25; . Epub 2018 Jul 25.
• Inherited gynaecological cancers.
  George A.Curr Opin Oncol. 2018 Jul 20; . Epub 2018 Jul 20.
• NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families.
  Al Shehhi M, Forman EB, Fitzgerald JE, McInerney V, Krawczyk J, Shen S, Betts DR, Ardle LM, Gorman KM, King MD, et al.Eur J Med Genet. 2018 Jul 18; . Epub 2018 Jul 18.

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This column displays citations pertaining to topics in medical genetics. See more filter information.