Results 211 to 220 of about 37,501 (261)

Molecular and clinical characteristics of glioma patients with germline pathogenic mutations of Lynch syndrome genes: a large-scale multicenter study. [PDF]

J Transl Med
Feng J, Ma T, Zhang X, Zhang Y, Qian Z, Dai Y, Gao Z, Zhao R, Yao C, Du G, Shao N, Wu Z, Ji N, Gu J, Liu Z, Yang Q, Sun X, Li W, Li X, Zhang Y, Ye Z, Yang A.   +21 more
europepmc   +1 more source

Yield of repeat gastric biopsies and Helicobacter pylori serological assessment in Lynch syndrome. [PDF]

Cancer Treat Res Commun
Vadaketh J, Konigsberg J, Elghawy O, Dinh K, Zhu L, Youngman J, Dungan M, Pulaski M, Long JM, Buckley KH, Katona BW.   +10 more
europepmc   +1 more source

NOUS-209 Off-the-shelf Immunotherapy Has the Potential to Hit Primary and Metachronous Colorectal and Urothelial Cancers in Lynch Syndrome. [PDF]

Mol Cancer Ther
De Marco L, Micarelli E, Panula J, Nikkola J, Moilanen L, Annala M, Härkönen J, Hokkanen KE, D'Alise AM, Pylvänäinen K, Peltomäki PT, Ahtiainen M, Böhm J, Mecklin JP, Scarselli E, Seppälä TT.   +15 more
europepmc   +1 more source

A missed opportunity for preventing CMMRD: is it time to include Lynch syndrome genes in prenatal genetic testing? [PDF]

BMJ Case Rep
Nair G, Cadenas N, Singh A.
europepmc   +1 more source

Uveal Melanoma and the Lynch Syndrome Tumor Spectrum.

JAMA Ophthalmol
Le Ven A, Villy MC, Silveira AB, Houy A, Masliah-Planchon J, Warcoin M, Le Mentec M, Simaga F, De Pauw A, Buecher B, Gauthier-Villars M, Verrier T, Merchadou K, Renault V, Vincent-Salomon A, Sauge J, El Zein S, Dubois d'Enghien C, Piperno-Neumann S, Matet A, Malaise D, Cassoux N, Lumbroso-Le Rouic L, Stoppa-Lyonnet D, Stern MH, Rodrigues M, Golmard L, Colas C.   +27 more
europepmc   +1 more source

Lynch syndrome: the patients perspective

Familial Cancer, 2013
People with Lynch syndrome have a high lifetime risk for the development of colorectal, endometrial and several other types of cancer. Lynch syndrome is caused by germline mutations in genes encoding DNA mismatch repair proteins. In this review, issues that concern Lynch patients are highlighted from the patients' perspective. Both authors are affected
Seppen, Jurgen, Bruzzone, Linda
openaire   +4 more sources

Lynch Syndrome

Surgical Pathology Clinics, 2016
Poster project on Lynch ...
Anne M. Mills, Teri A. Longacre
core   +4 more sources

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Lynch syndrome

Journal of the American Academy of Physician Assistants, 2011
Almost 100 years ago Lynch syndrome was discovered by Dr Aldred Warthin. Initially, the syndrome was named Hereditary Nonpolyposis Colorectal Cancer as colorectal cancer seemed most prevalent. Over time uterine cancer and several other malignancies were recognized as part of the spectrum.
Floor J, Backes, David E, Cohn
  +6 more sources

Identification of Lynch Syndrome

Gastrointestinal Endoscopy Clinics of North America, 2022
Lynch syndrome (LS) is an autosomal dominant hereditary cancer syndrome caused by pathogenic germline variants (PGV) in any of the 4 DNA mismatch repair (MMR) genes, MLH1, MSH2, MSH6, and PMS2, or deletions in EPCAM. LS leads to an increased risk of intestinal and extraintestinal cancers, of which colorectal and endometrial cancers are the most common.
Jennifer K, Maratt, Elena, Stoffel
openaire   +2 more sources

Lynch Syndrome

, 2015
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Ivan R. Rohena-Quinquilla, Lattin Grant, Darcy J. Wolfman   +2 more
openaire   +2 more sources