Works matching Diagnosis of hereditary nonpolyposis colorectal cancer

Results: 147

Molecular diagnosis of hereditary nonpolyposis colorectal cancer.

Published in:

1999

By:

O'Leary, Timothy J.;
O'Leary, T J

Publication type:

Editorial

Toward a Consensus in Molecular Diagnosis of Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome).

Published in:

2007

By:

Lynch, Henry T.;
Lynch, Jane F.;
Lynch, Patrick M.

Publication type:

Editorial

Lynch syndrome: following the leads to save lives.

Published in:

2024

By:

Coughlan, Claire

Publication type:

Editorial

MAKE A LONG STORY SHORT: IMPORTANCE OF GENETIC TESTING IN DIAGNOSIS OF LYNCH SYNDROME -- A CASE REPORT.

Published in:

Acta Marisiensis. Seria Medica, 2024, v. 70, p. 241

By:

Gombár, Anna;
Burz, Claudia-Cristina

Publication type:

Article

Inherited Mutations Are More Common Than Thought in Early-Onset Colorectal Cancer.

Published in:: ONS Voice, 2017, v. 32, n. 2, p. 8
Publication type:: Article

Prevalence and Prognosis of Lynch Syndrome and Sporadic Mismatch Repair Deficiency in Endometrial Cancer.

Published in:

2021

By:

Post, Cathalijne C B;
Stelloo, Ellen;
Smit, Vincent T H B M;
Ruano, Dina;
Tops, Carli M;
Vermij, Lisa;
Rutten, Tessa A;
Jürgenliemk-Schulz, Ina M;
Lutgens, Ludy C H W;
Jobsen, Jan J;
Nout, Remi A;
Crosbie, Emma J;
Powell, Melanie E;
Mileshkin, Linda;
Leary, Alexandra;
Bessette, Paul;
Putter, Hein;
Boer, Stephanie M de;
Horeweg, Nanda;
Nielsen, Maartje

Publication type:

journal article

Comparison of Prediction Models for Lynch Syndrome Among Individuals With Colorectal Cancer.

Published in:

2016

By:

Kastrinos, Fay;
Ojha, Rohit P.;
Leenen, Celine;
Alvero, Carmelita;
Mercado, Rowena C.;
Balmaña, Judith;
Valenzuela, Irene;
Balaguer, Francesc;
Green, Roger;
Lindor, Noralane M.;
Thibodeau, Stephen N.;
Newcomb, Polly;
Aung Ko Win;
Jenkins, Mark;
Buchanan, Daniel D.;
Bertario, Lucio;
Sala, Paola;
Hampel, Heather;
Syngal, Sapna;
Steyerberg, Ewout W.

Publication type:

journal article

Choosing not to undergo predictive genetic testing for hereditary colorectal cancer syndromes: expanding our understanding of decliners and declining.

Published in:

Journal of Behavioral Medicine, 2017, v. 40, n. 4, p. 583, doi. 10.1007/s10865-016-9820-0

By:

Keogh, Louise;
Niven, Heather;
Rutstein, Alison;
Flander, Louisa;
Gaff, Clara;
Jenkins, Mark

Publication type:

Article

Impact of universal immunohistochemistry on Lynch syndrome diagnosis in an Australian colorectal cancer cohort.

Published in:

Internal Medicine Journal, 2019, v. 49, n. 10, p. 1278, doi. 10.1111/imj.14230

By:

Loh, Zoe;
Williams, David S.;
Salmon, Lucinda;
Dow, Eryn;
John, Thomas

Publication type:

Article

Clinicopathological Features and Management of Cancers in Lynch Syndrome.

Published in:

Pathology Research International, 2012, p. 1, doi. 10.1155/2012/350309

By:

Aarnio, Markku

Publication type:

Article

Prevalence and Correlates of Receiving and Sharing High-Penetrance Cancer Genetic Test Results: Findings from the Health Information National Trends Survey.

Published in:

Public Health Genomics, 2015, v. 18, n. 2, p. 67, doi. 10.1159/000368745

By:

Taber, Jennifer M.;
Chang, Christine Q.;
Lam, Tram K.;
Gillanders, Elizabeth M.;
Hamilton, Jada G.;
Schully, Sheri D.

Publication type:

Article

Underutilization of Lynch Syndrome Screening at Two Large Veterans Affairs Medical Centers.

Published in:

2020

By:

Mittal, Chetan;
Dang, Duyen;
Stoffel, Elena;
Menees, Stacy;
Scott, Frank I.;
Ahnen, Dennis;
Patel, Swati G.

Publication type:

journal article

Keys to identifying Lynch syndrome: Two cases illustrate the importance of and challenges inherent in diagnosing this under-diagnosed hereditary cancer syndrome in your patients.

Published in:

2018

By:

KIRKPATRICK, DOUGLAS H.;
COTTON, VICTOR R.

Publication type:

Case Study

HBOC and Lynch syndrome testing: All in a day's work: Ob/gyns have a responsibility and can no longer be passive in this genomic era.

Published in:

2018

By:

SIMPSON, JOE LEIGH

Publication type:

Editorial

Lynch Syndrome.

Published in:

Contemporary OB/GYN, 2015, v. 60, n. 5, p. 33

By:

Shulman, Lee P.

Publication type:

Article

The predicted impact and cost-effectiveness of systematic testing of people with incident colorectal cancer for Lynch syndrome.

Published in:

2020

By:

Kang, Yoon‐Jung;
Killen, James;
Caruana, Michael;
Simms, Kate;
Taylor, Natalie;
Frayling, Ian M;
Snowsill, Tristan;
Huxley, Nicola;
Coupe, Veerle MH;
Hughes, Suzanne;
Freeman, Victoria;
Boussioutas, Alex;
Trainer, Alison H;
Ward, Robyn L;
Mitchell, Gillian;
Macrae, Finlay A;
Canfell, Karen;
Kang, Yoon-Jung

Publication type:

journal article

The added value of PMS2 immunostaining in the diagnosis of hereditary nonpolyposis colorectal cancer.

Published in:

Familial Cancer, 2006, v. 5, n. 4, p. 353, doi. 10.1007/s10689-006-0005-9

By:

Halvarsson, Britta;
Lindblom, Annika;
Rambech, Eva;
Lagerstedt, Kristina;
Nilbert, Mef

Publication type:

Article

MR findings of Lynch syndrome-related uterine endometrial carcinoma: a case report.

Published in:

Abdominal Radiology, 2016, v. 41, n. 9, p. 1703, doi. 10.1007/s00261-016-0721-z

By:

Minamiguchi, Kiyoyuki;
Takahama, Junko;
Marugami, Nagaaki;
Marugami, Aki;
Haga, Masayo;
Takewa, Megumi;
Itoh, Takahiro;
Kichikawa, Kimihiko;
Uchiyama, Tomoko

Publication type:

Article

Tumor Molecular Testing Guides Anti‐PD‐1 Therapy and Provides Evidence for Pathogenicity of Mismatch Repair Variants.

Published in:

Oncologist, 2018, v. 23, n. 12, p. 1395, doi. 10.1634/theoncologist.2018-0108

By:

Patel, Shyam A.;
Longacre, Teri A.;
Ladabaum, Uri;
Lebensohn, Alexandra;
Lin, Albert Y.;
Haraldsdottir, Sigurdis

Publication type:

Article

The Importance of Distinguishing Sporadic Cancers from Those Related to Cancer Predisposing Germline Mutations.

Published in:

Oncologist, 2018, v. 23, n. 11, p. 1266, doi. 10.1634/theoncologist.2017-0681

By:

Sorscher, Steven

Publication type:

Article

Let's talk menopause.

Published in:

Journal of Community Nursing, 2023, v. 37, n. 2, p. 4

By:

Bades, Annette

Publication type:

Article

Hereditary colorectal cancer and Lynch syndrome.

Published in:

BMC Proceedings, 2013, v. 7, n. Suppl 2, p. 1, doi. 10.1186/1753-6561-7-S2-K2

By:

Rossi, Benedito M.

Publication type:

Article

High Tumor Microsatellite Instability a Marker for Lynch Syndrome, More Common Condition Than Generally Expected.

Published in:

American Health & Drug Benefits, 2018, v. 11, p. 36

By:

Kuznar, Wayne

Publication type:

Article

Hereditary Nonpolyposis Colorectal Cancer (HNPCC)/Lynch Syndrome.

Published in:

2013

By:

Gupta, Robin Sen;
Steinke, Verena;
Propping, Peter;
Engel, Christoph;
Büttner, Reinhard;
Schackert, Konrad;
Schmiegel, Wolf H.

Publication type:

Letter

Hereditary Nonpolyposis Colorectal Cancer (HNPCC)/Lynch Syndrome.

Published in:

Deutsches Ärzteblatt International, 2013, v. 110, n. 3, p. 32, doi. 10.3238/arztebl.2013.0032

By:

Steinke, Verena;
Engel, Christoph;
Büttner, Reinhard;
Schackert, Hans Konrad;
Schmiegel, Wolff H.;
Propping, Peter

Publication type:

Article

Two cases of successful pregnancies after hysteroscopic removal of endometrioid adenocarcinoma grade I, stage IA, in young women with Lynch syndrome.

Published in:

2014

By:

Marton, Ingrid;
Vranes, Hrvojka Soljacic;
Sparac, Vladimir;
Maricic, Igor;
Kuna, Krunoslav;
Kopjar, Miroslav

Publication type:

Case Study

Guidelines on Genetic Evaluation and Management of Lynch Syndrome: A Consensus Statement by the US Multi-Society Task Force on Colorectal Cancer.

Published in:

American Journal of Gastroenterology (Springer Nature), 2014, v. 109, n. 8, p. 1159, doi. 10.1038/ajg.2014.186

By:

Giardiello, Francis M;
Allen, John I;
Axilbund, Jennifer E;
Boland, C Richard;
Burke, Carol A;
Burt, Randall W;
Church, James M;
Dominitz, Jason A;
Johnson, David A;
Kaltenbach, Tonya;
Levin, Theodore R;
Lieberman, David A;
Robertson, Douglas J;
Syngal, Sapna;
Rex, Douglas K

Publication type:

Article

Ovarian metastasis from uveal melanoma with MLH1/PMS2 protein loss in a patient with germline MLH1 mutated Lynch syndrome: consequence or coincidence?

Published in:

2017

By:

Lobo, João;
Pinto, Carla;
Freitas, Micaela;
Pinheiro, Manuela;
Vizcaino, Rámon;
Oliva, Esther;
Teixeira, Manuel;
Jerónimo, Carmen;
Bartosch, Carla;
Teixeira, Manuel R

Publication type:

journal article

Immunohistochemical staining for p16 and BRAFV600E is useful to distinguish between sporadic and hereditary (Lynch syndrome-related) microsatellite instable colorectal carcinomas.

Published in:

2016

By:

Boissière-Michot, Florence;
Frugier, Hélène;
Ho-Pun-Cheung, Alexandre;
Lopez-Crapez, Evelyne;
Duffour, Jacqueline;
Bibeau, Frédéric;
Boissière-Michot, Florence;
Frugier, Hélène;
Bibeau, Frédéric

Publication type:

journal article

Genetic Disorder Reference Sheet: Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer).

Published in:

ONS Voice, 2024, p. 1

By:

Mahon, Suzanne M.

Publication type:

Article

Endometrial carcinoma-related genetic factors: application to research and clinical practice in China.

Published in:

2016

By:

Zhou, JY;
Zhang, L;
Wei, LH;
Wang, JL

Publication type:

journal article

Cost-effectiveness of DNA testing for Lynch syndrome for colorectal cancer patients in Switzerland.

Published in:

European Journal of Public Health, 2021, v. 31, p. iii464

By:

Salikhanov, I.;
Wieser, S.;
Katapodi, M.

Publication type:

Article

Feasibility of Utilizing PREMM Score for Lynch Syndrome Identification in an Urban, Minority Patient Population.

Published in:

Journal of Primary Care & Community Health, 2021, p. 1, doi. 10.1177/21501327211020973

By:

Adviento, Brigid;
Conner, Michael;
Sarkisian, Alexander;
Walano, Nicolette;
Andersson, Hans;
Karlitz, Jordan

Publication type:

Article

Corrigendum to Feasibility of Utilizing PREMM Score for Lynch Syndrome Identification in an Urban, Minority Patient Population.

Published in:: 2021
Publication type:: Correction Notice

Feasibility of Utilizing PREMM Score for Lynch Syndrome Identification in an Urban, Minority Patient Population.

Published in:

Journal of Primary Care & Community Health, 2021, p. 1, doi. 10.1177/21501327211020973

By:

Adviento, Brigid;
Conner, Michael;
Sarkisian, Alexander;
Walano, Nicolette;
Andersson, Hans;
Karlitz, Jordan

Publication type:

Article

Lynch Syndrome Testing: A Missed Opportunity in the Era of Precision Medicine.

Published in:

2016

By:

Pasche, Boris;
Pennison, Michael J;
DeYoung, Barry

Publication type:

commentary

Lynch Syndrome Testing.

Published in:

2016

By:

Pasche, Boris;
Pennison, Michael J.;
DeYoung, Barry

Publication type:

Editorial

Tumor Screening and DNA Testing in the Diagnosis of Lynch Syndrome.

Published in:

2016

By:

Usha, Lydia;
Dewdney, Summer B.;
Buckingham, Lela E.

Publication type:

journal article

Colorectal cancer genetic referral: Are we doing enough?

Published in:

Baylor University Medical Center Proceedings, 2024, v. 37, n. 2, p. 250, doi. 10.1080/08998280.2024.2303529

By:

Broyles, Whitnee C.;
Narvekar, Priyanka;
Lee, Hanjoo;
Fleshman, James W.;
Fichera, Alessandro;
Wells, Katerina K. O.

Publication type:

Article

The genetic etiology of familial and nonfamilial colorectal cancer.

Published in:

2011

By:

Cherry, Lorraine M.

Publication type:

Journal Article

Supporting patients undergoing genomic testing for Lynch syndrome as part of their diagnostic cancer pathway.

Published in:

Cancer Nursing Practice, 2024, v. 23, n. 4, p. 34, doi. 10.7748/cnp.2024.e1859

By:

John, Siobhan

Publication type:

Article

Screening for Lynch Syndrome Among Patients with Colorectal Cancer: Experiences from a Multihospital Health System.

Published in:

Journal of Clinical Outcomes Management, 2018, v. 25, n. 10, p. 451

By:

Salner, Andrew;
Sekerak, Richard;
Yu, Peter Paul

Publication type:

Article

AGO Austria recommendation on screening and diagnosis of Lynch syndrome (LS).

Published in:

2017

By:

Zeimet, Alain;
Mori, Harald;
Petru, Edgar;
Polterauer, Stephan;
Reinthaller, Alexander;
Schauer, Christian;
Scholl-Firon, Tonja;
Singer, Christian;
Wimmer, Katharina;
Zschocke, Johannes;
Marth, Christian;
Zeimet, Alain G

Publication type:

journal article

Same MSH2 Gene Mutation But Variable Phenotypes in 2 Families With Lynch Syndrome: Two Case Reports and Review of Genotype-Phenotype Correlation.

Published in:

Clinical Medicine Insights: Case Reports, 2018, n. 11, p. 1, doi. 10.1177/1179547617753943

By:

Liccardo, Raffaella;
De Rosa, Marina;
Duraturo, Francesca

Publication type:

Article

How does genetic risk information for Lynch syndrome translate to risk management behaviours?

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-016-0061-6

By:

Steel, Emma;
Robbins, Andrew;
Jenkins, Mark;
Flander, Louisa;
Gaff, Clara;
Keogh, Louise

Publication type:

Article

Lynch syndrome.

Published in:

JAAPA: Journal of the American Academy of Physician Assistants (Haymarket Media, Inc.), 2011, v. 24, n. 7, p. 61, doi. 10.1097/01720610-201107000-00017

By:

MICHAUD, ED

Publication type:

Article

Genetic Predisposition and Multifocal Cancer: A Complex Case of Lynch Syndrome.

Published in:

ACG Case Reports Journal, 2025, v. 12, n. 6, p. 1, doi. 10.14309/crj.0000000000001718

By:

Glover, Caleb;
Russell, Claire;
Rida, Ali;
Bhatnagar, Shweta;
Cay, Edward;
Nguyen, Eric;
Davies, Alexandra;
Ross, Albert

Publication type:

Article

Thyroid imaging reporting and data system in assessment of cytological Bethesda Category III thyroid nodules.

Published in:

Clinical Hemorheology & Microcirculation, 2017, v. 65, n. 2, p. 163, doi. 10.3233/CH-16146

By:

Feng Mao;
Hui-Xiong Xu;
Chong-Ke Zhao;
Xiao-Wan Bo;
Xiao-Long Li;
Dan-Dan Li;
Bo-Ji Liu;
Yi-Feng Zhang;
Jun-Mei Xu;
Shen Qu

Publication type:

Article

Predictive model for high-frequency microsatellite instability in colorectal cancer patients over 50 years of age.

Published in:

Cancer Medicine, 2017, v. 6, n. 6, p. 1255, doi. 10.1002/cam4.1088

By:

Fujiyoshi, Kenji;
Yamaguchi, Tatsuro;
Kakuta, Miho;
Takahashi, Akemi;
Arai, Yoshiko;
Yamada, Mina;
Yamamoto, Gou;
Ohde, Sachiko;
Takao, Misato;
Horiguchi, Shin ‐ ichiro;
Natsume, Soichiro;
Kazama, Shinsuke;
Nishizawa, Yusuke;
Nishimura, Yoji;
Akagi, Yoshito;
Sakamoto, Hirohiko;
Akagi, Kiwamu

Publication type:

Article

Gene-environment interaction in hereditary nonpolyposis colorectal cancer with implications for diagnosis and genetic testing.

Published in:

International Journal of Cancer, 1999, v. 82, n. 4, p. 516, doi. 10.1002/(SICI)1097-0215(19990812)82:4<516::AID-IJC8>3.0.CO;2-U

By:

Park, Jae-Gahb;
Park, Young Jin;
Wijnen, Juul T.;
Vasen, Hans F.A.

Publication type:

Article