Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Anne-Sophie van der Werf –'t Lam"'
Autor:
Noah c. Helderman, Anne-Sophie Van Der Werf-’T Lam, Hans Morreau, Arnoud Boot, Tom Van Wezel, Maartje Nielsen, Diantha Terlouw, Sanne W. Bajwa-ten Broeke, Mar Rodríguez-Girondo, Demi van Egmond, Alexandra M.J. Langers, Monique E. van Leerdam, Emily Rayner, Christi J. van Asperen, Liselotte P. van Hest, Hans J.P. Gille, Floor A.M. Duijkers, Anja Wagner, Ellis L. Eikenboom, Tom G.W. Letteboer, Mirjam M. de Jong, Fonnet E. Bleeker, Encarna B. Gomez Garcìa, Manon Suerink, Carli M. Tops, Niels de Wind
Publikováno v:
MSH6 TUMOR GROUP 2023, ' Molecular Profile of MSH6-Associated Colorectal Carcinomas Shows Distinct Features From Other Lynch Syndrome–Associated Colorectal Carcinomas ', Gastroenterology, vol. 165, no. 1, pp. 271-274.e2 . https://doi.org/10.1053/j.gastro.2023.03.198
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1acb9f5b21ff316ff9b4e61fd4dd4b08
http://www.scopus.com/inward/record.url?scp=85160215499&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=85160215499&partnerID=8YFLogxK
Autor:
Winand N.M. Dinjens, Robert M.W. Hofstra, Monique E. van Leerdam, Maartje Nielsen, Manon C.W. Spaander, Hans Morreau, Anne-Sophie van der Werf –’t Lam, Ellis L. Eikenboom, Mar Rodríguez-Girondo, Christi J. van Asperen, Anja Wagner
Publikováno v:
Clinical Gastroenterology and Hepatology, 20(3), e496-e507. W.B. Saunders
Clinical Gastroenterology and Hepatology, 20(3), E496-E507. ELSEVIER SCIENCE INC
Clinical Gastroenterology and Hepatology, 20(3), E496-E507. ELSEVIER SCIENCE INC
Background & Aims: Lynch syndrome is a form of hereditary colorectal cancer (CRC) caused by pathogenic germline variants (PV) in DNA mismatch repair (MMR) genes. Currently, many Western countries perform universal immunohistochemistry testing on CRC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ed04eeda5d3456314e75c520109d93d
https://hdl.handle.net/1887/3294542
https://hdl.handle.net/1887/3294542
Autor:
Maartje Nielsen, Diantha Terlouw, Manon Suerink, Sanne W. ten Broeke, Anne-Sophie van der Werf-’ t Lam, Noah C. Helderman, Tom van Wezel, Hans Morreau
Publikováno v:
Critical Reviews in Oncology/Hematology, 163. ELSEVIER SCIENCE INC
Lynch syndrome (LS) is a hereditary cancer syndrome that accounts for 3% of all new colorectal cancer (CRC) cases. Patients carry a germline pathogenic variant in one of the mismatch repair (MMR) genes (MLH1, MSH2, MSH6 or PMS2), which encode protein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11bc023e9d0fe809477fdc3a4839975c
https://doi.org/10.1016/j.critrevonc.2021.103338
https://doi.org/10.1016/j.critrevonc.2021.103338
Autor:
Regina Bökenkamp-Gramann, Daniela Q.C.M. Barge-Schaapveld, Monique Williams, Julie W. Rutten, Karin van der Tuin, Esther A. R. Nibbeling, Claudia A. L. Ruivenkamp, Sylke J. Steggerda, Laura Donker Kaat, Dietje E. Fransen van de Putte, Remco van Doorn, Marjolein Kriek, Ruben S G M Witlox, Maartje van Rij, Cacha M.P.C.D. Peeters-Scholte, Arie van Haeringen, Thomas P. Potjer, Emilia K. Bijlsma, Setareh Moghadasi, Yvette van Ierland, Manon Suerink, Emmelien Aten, Gijs W. E. Santen, Remco Visser, Anne Sophie van der Werf–t Lam, Mariëtte J.V. Hoffer, Marije Koopmans, Pleuntje J. van der Sluijs, Ratna N G B Tan, Nicolette S. den Hollander, Arend D. J. ten Harkel, Yvonne Hilhorst-Hofstee
Publikováno v:
Genetics in Medicine. 21:2159-2164
The original version of this Article contained an error in the spelling of the author Pleuntje J. van der Sluijs, which was incorrectly given as Eline (P. J.) van der Sluijs. This has now been corrected in both the PDF and HTML versions of the Articl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcea68d20998bde8f8bee4e1a815b939
https://doi.org/10.1038/s41436-018-0363-3
https://doi.org/10.1038/s41436-018-0363-3
Autor:
Setareh Moghadasi, Emilia K. Bijlsma, Remco van Doorn, Monique Williams, Maartje van Rij, Remco Visser, Thomas P. Potjer, Arend D. J. ten Harkel, Yvette van Ierland, Laura Donker Kaat, Emmelien Aten, Daniela Q.C.M. Barge-Schaapveld, Cacha M.P.C.D. Peeters-Scholte, Nicolette S. den Hollander, Ratna N G B Tan, Ruben S G M Witlox, Regina Bökenkamp-Gramann, Julie W. Rutten, Manon Suerink, Marjolein Kriek, Yvonne Hilhorst-Hofstee, Sylke J. Steggerda, Mariëtte J.V. Hoffer, Marije Koopmans, Pleuntje J. van der Sluijs, Anne-Sophie van der Werf –’t Lam, Gijs W. E. Santen, Claudia A. L. Ruivenkamp, Dietje E. Fransen van de Putte, Arie van Haeringen, Karin van der Tuin, Esther A. R. Nibbeling
Publikováno v:
Genetics in Medicine, 21(5), 1074-1082. Lippincott Williams & Wilkins
Genetics in Medicine, 21(5), 1074-1082
Genetics in Medicine
Genetics in medicine, 21(5), 1074-1082. Lippincott Williams and Wilkins
Genetics in Medicine, 21(5), 1074-1082
Genetics in Medicine
Genetics in medicine, 21(5), 1074-1082. Lippincott Williams and Wilkins
Purpose: Several studies have reported diagnostic yields up to 57% for rapid exome or genome sequencing (rES/GS) as a single test in neonatal intensive care unit (NICU) patients, but the additional yield of rES/GS compared with other available diagno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1be1375788cf6ae5d4c97f805a4d15f1
https://hdl.handle.net/1765/110952
https://hdl.handle.net/1765/110952