Zobrazeno 1 - 10 of 239 pro vyhledávání: '"Sijmons R"'
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Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome
Autor: Tischkowitz, M, Colas, C, Pouwels, S, Hoogerbrugge, N, Ligtenberg, M, Oostenbrink, Rianne, Sijmons, R, Evans, G, Woodward, E, Peltonen, S, Hietala, M
Publikováno v: European Journal of Human Genetics, 28, 1387-1393
Semple, R K 2020, ' Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome ', European Journal of Human Genetics . https://doi.org/10.1038/s41431-020-0651-7
European Journal of Human Genetics, 28(10), 1387-1393. Nature Publishing Group
European Journal of Human Genetics, 28, 10, pp. 1387-1393
EUROPEAN JOURNAL OF HUMAN GENETICS
European Journal of Human Genetics
Contains fulltext : 225252.pdf (Publisher’s version ) (Open Access) PTEN hamartoma tumour syndrome is a diverse multi-system disorder predisposing to the development of hamartomatous growths, increasing risk of breast, thyroid, renal cancer, and po
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0ca7f01c9a5953a5a2debf53d05dbf4
https://doi.org/10.1038/s41431-020-0651-7
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Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database (Genetics in Medicine, (2020), 22, 1, (15-25), 10.1038/s41436-019-0596-9)
Autor: Dominguez-Valentin M., Sampson J. R., Seppala T. T., ten Broeke S. W., Plazzer J. -P., Nakken S., Engel C., Aretz S., Jenkins M. A., Sunde L., Bernstein I., Capella G., Balaguer F., Thomas H., Evans D. G., Burn J., Greenblatt M., Hovig E., de Vos tot Nederveen Cappel W. H., Sijmons R. H., Bertario L., Tibiletti M. G., Cavestro G. M., Lindblom A., Della Valle A., Lopez-Kostner F., Gluck N., Katz L. H., Heinimann K., Vaccaro C. A., Buttner R., Gorgens H., Holinski-Feder E., Morak M., Holzapfel S., Huneburg R., Knebel Doeberitz M., Loeffler M., Rahner N., Schackert H. K., Steinke-Lange V., Schmiegel W., Vangala D., Pylvanainen K., Renkonen-Sinisalo L., Hopper J. L., Win A. K., Haile R. W., Lindor N. M., Gallinger S., Le Marchand L., Newcomb P. A., Figueiredo J. C., Thibodeau S. N., Wadt K., Therkildsen C., Okkels H., Ketabi Z., Moreira L., Sanchez A., Serra-Burriel M., Pineda M., Navarro M., Blanco I., Green K., Lalloo F., Crosbie E. J., Hill J., Denton O. G., Frayling I. M., Rodland E. A., Vasen H., Mints M., Neffa F., Esperon P., Alvarez K., Kariv R., Rosner G., Pinero T. A., Gonzalez M. L., Kalfayan P., Tjandra D., Winship I. M., Macrae F., Moslein G., Mecklin J. -P., Nielsen M., Moller P.
The original version of this Article did not contain details of Dutch Cancer Society (DCS) funding (grant number UL 2017-8223) in the Acknowledgements section. This has now been corrected in both the PDF and HTML versions of the Article.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_____10495::3129dc2a5e9324bd9fb714050181cb67
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Reply to Kratz et al
Autor: Frebourg, T, Lagercrantz, SB, Oliveira, C, Magenheim, R, Evans, DGR, Hoogerbrugge, N, Ligtenberg, M, Oostenbrink, Rianne, Sijmons, R, Evans, G, Woodward, E, Peltonen, S, Hietala, M
Publikováno v: European Journal of Human Genetics
European Journal of Human Genetics, 28, 11, pp. 1483-1485
European Journal of Human Genetics, 28, 1483-1485
European Journal of Human Genetics, 28(11), 1483-1485. Nature Publishing Group
Contains fulltext : 229308.pdf (Publisher’s version ) (Open Access)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a5d41d7c4a56d112441b0381629e4c5
http://europepmc.org/articles/PMC7576774
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Analysis in the Prospective Lynch Syndrome Database identifies sarcoma as part of the Lynch syndrome tumor spectrum
Autor: Dominguez-Valentin M., Sampson J. R., Moller P., Seppala T. T., Plazzer J. -P., Nakken S., Engel C., Aretz S., Jenkins M. A., Sunde L., Bernstein I., Capella G., Balaguer F., Thomas H., Evans D. G., Burn J., Greenblatt M., Hovig E., Nielsen M., de Vos tot Nederveen Cappel W. H., Sijmons R. H., Bertario L., Tibiletti M. G., Cavestro G. M., Lindblom A., Valle A. D., Lopez-Kostner F., Gluck N., Katz L. H., Heinimann K., Vaccaro C. A., Buttner R., Gorgens H., Holinski-Feder E., Morak M., Holzapfel S., Huneburg R., von Knebel Doeberitz M., Loeffler M., Rahner N., Weitz J., Steinke-Lange V., ten Broeke S. W., Schmiegel W., Vangala D., Pylvanainen K., Renkonen-Sinisalo L., Hopper J. L., Win A. K., Haile R. W., Lindor N. M., Gallinger S., Le Marchand L., Newcomb P. A., Figueiredo J. C., Thibodeau S. N., Jensen L. H., Madsen M. B., Kroldrup L., Nilbert M., Moreira L., Sanchez A., Serra-Burriel M., Pineda M., Navarro M., Vidal J. B., Blanco I., Green K., Lalloo F., Crosbie E. J., Hill J., Denton O. G., Rodland E. A., Vasen H., Mints M., Neffa F., Esperon P., Alvarez K., Kariv R., Rosner G., Pinero T. A., Gonzalez M. L., Kalfayan P., Tjandra D., Winship I. M., Macrae F., Moslein G., Mecklin J. -P.
Publikováno v: Dominguez-Valentin, M, Sampson, J R, Møller, P, Seppälä, T T, PLSD Collaborators, Sunde, L & Bernstein, I 2021, ' Analysis in the Prospective Lynch Syndrome Database identifies sarcoma as part of the Lynch syndrome tumor spectrum ', International Journal of Cancer, vol. 148, no. 2, pp. 512-513 . https://doi.org/10.1002/ijc.33214
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::256db311728c9b8d2ebfdfd70b7043e2
https://doi.org/10.1002/ijc.33214
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Personalized medicine via Pharmacogenetics: Investigating critical success factors for clinical implementation
Autor: Plantinga, M., Van Langen, I., Ranchor, A., Lanting, P., Wilffert, B., Sijmons, R.
Publikováno v: None
Background and aim: Pharmacogenetics (PGx) has the potential to improve drug efficacy and safety by identifying patients likely to respond well to a certain drug or who could be at risk. Although substantial evidence has been published to support the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=narcis______::8f73ec2f64e54a9d7407802b2f7a54d5
https://research.rug.nl/en/publications/b8da3e65-eb7c-44f0-9095-cb1af312080c
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Boosting care and knowledge about hereditary cancer: European Reference Network on Genetic Tumour Risk Syndromes
Autor: Vos, JR, Giepmans, L, Rohl, C, Geverink, N, Hoogerbrugge, N, Ligtenberg, M, Kets, M, Sijmons, R, Evans, G, Woodward, E, Tischkowitz, M, Maher, E, Steinke-Lange, V, Holinski-Feder, E, Frebourg, T, Houdayer, C, Ferner, RE, Lubinski, J, Ertmanska, K, Lagercrantz, SB, Tham, E, Guillermo, IB, Capella, G, Vidal, JB, Lazaro, C (Conxi), Balmana, J, Bours, V, Legius, E, Wolkenstein, P, Melegh, B, Oliveira, C, Teixeira, M, Poppe, B, Claes, K, Hernandez, HS, Aretz, AWM, Spier, I, Oostenbrink, Rianne, Krajc, M, Blatnik, A, Schrock, E, Peltonen, S, Hietala, M, Ern, G
Publikováno v: Vos, JR, Giepmans, L, Röhl, C, Geverink, N, Hoogerbrugge, N, ERN, GENTURIS & Evans, D G 2019, ' Boosting care and knowledge about hereditary cancer: European Reference Network on Genetic Tumour Risk Syndromes. ', Familial Cancer . https://doi.org/10.1007/s10689-018-0110-6
Familial Cancer, 18(2), 281-284. SPRINGER
Familial Cancer, 18(2), 281-284. Springer Netherlands
Familial Cancer
Familial Cancer, 18, 281-284
Familial Cancer, 18, 2, pp. 281-284
FAMILIAL CANCER
Approximately 27-36 million patients in Europe have one of the ~ 5.000-8.000 known rare diseases. These patients often do not receive the care they need or they have a substantial delay from diagnosis to treatment. In March 2017, twenty-four European
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee01440d9c450a349db2b80095a24994
http://europepmc.org/abstract/med/30302652
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