Results 121 to 130 of about 1,289,326 (214)
"Dvr. A W Lynch VX 69280 2/107 Aust. General Transport 1942 -1943 - Adelaide River Fenton Airfield".Driver A. W. Lynch VX 69280. 2/107 Australian General Transport 1942 -1943.
Lynch, A. W.
core
The Role of “Adult‐Onset” Cancer Predisposition Genes in Pediatric Cancer: A Comprehensive Review
ABSTRACT Current literature estimates that 10% of pediatric cancers are caused by pathogenic or likely pathogenic (P/LP) germline variants in cancer predisposition genes (CPGs). Variants in CPGs thought to increase cancer risk exclusively during adulthood are referred to as “adult‐onset” CPGs (aoCPGs).
Maria Rozo +5 more
wiley +1 more source
Raffaella Liccardo,1 Carlo Della Ragione,2 Nunzio Mitilini,2 Marina De Rosa,1 Paola Izzo,1 Francesca Duraturo11Department of Molecular Medicine and Medical Biotechnologies, School of Medicine, University of Naples “Federico II”, Naples, Italy;
Liccardo R +5 more
doaj
Using a multicenter Japanese colorectal cancer cohort from 25 institutions, we analyzed 1464 patients across all disease stages and tumor locations to determine the prevalence and clinicopathological features of MSI‐H/dMMR colorectal cancer. MSI‐H/dMMR tumors accounted for 9.4% of cases overall, were present in 22% of right‐sided colon cancers, and ...
Yoshihiro Morimoto +27 more
wiley +1 more source
ABSTRACT Mosunetuzumab plus polatuzumab vedotin has shown promising activity versus rituximab plus polatuzumab vedotin (R‐Pola) in patients with relapsed/refractory (R/R) large B‐cell lymphoma (LBCL; NCT03671018). We present results from the Phase II randomized cohort, evaluating subcutaneous mosunetuzumab plus polatuzumab vedotin (Mosun‐Pola), with ...
Julio C. Chavez +17 more
wiley +1 more source
Les critères diagnostiques du syndrome de Lynch
Le syndrome de Lynch est décrit depuis longtemps et il est le plus fréquent des syndromes de prédisposition génétique au cancer du côlon, mais il reste très mal connu aujourd’hui.
Janin, Nicolas
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Lynch syndrome in the Asian populations
© 2016 Dr. Chun How GanLynch syndrome is an autosomal dominant genetic disorder. Mutation carriers are at significant risk of developing colorectal and a variety of extra-colonic cancers, often at a younger age compared to sporadic cancers.
Gan, Chun How
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ABSTRACT A 63‐year‐old man presented with melena and severe anemia 18 years after nephrectomy for clear cell renal cell carcinoma. Imaging and biopsy confirmed duodenal and pancreatic metastases mimicking pancreaticobiliary malignancy. He underwent pancreaticoduodenectomy.
Ankit Kulkarni +6 more
wiley +1 more source
Transitioning from the Prospective Lynch Syndrome Database (PLSD) to the International Lynch Syndrome Database (ILSD). [PDF]
Dominguez-Valentin M.
europepmc +1 more source
Structured surveillance in Lynch syndrome: effectiveness, limitations, and unmet needs. [PDF]
Dardenne A +12 more
europepmc +1 more source

