Zobrazeno 1 - 10
of 349
pro vyhledávání: '"Ligtenberg, M."'
Autor:
Vergote, I., Ausems, M., Brasiuniene, B., Brenton, J., Büttner, R., Colombo, N., González-Martín, A., Harter, P., Lambrechts, D., Lorusso, D., Madry, R., Mirza, M.R., Pujol, P., Ray-Coquard, I., Abreu, M., Balboni, S., Banerjee, S., Barberis, M., Barretina Ginesta, M.P., Baurain, J.-F., Bignami, M., Bjorge, L., Blecharz, P., Bruchim, I., Capilna, M., Cerana, N., Cicchetti, A., Collins, D., Concin, N., D’Incalci, M., Davidson, B., de la Motte Rouge, T., De Iaco, P., Demirkiran, F., Denys, H., Doerk, T., Dorum, A., Ferrero, A., Fidalgo, A.P., Genuardi, M., Gladieff, L., Glasspool, R., Grimm, C., Gultekin, M., Hahnen, E., Hasenburg, A., Hegmane, A., Heinzelmann, V., Hogdall, E., Janavicius, R., Jarmalaite, S., Kalachand, R., Kaneva, R., Kilickap, S., Kocian, R., Kolencik, D., Kristeleit, R., Kryzhanivska, A., Leary, A., Lemley, B., Ligtenberg, M., López-Guerrero, J.A., Lord, C.J., Avall-Lundqvist, E., Maenpaa, J., Mahner, S., Marmé, F., Marth, C., McNeish, I., Merkelbach-Bruse, S., Mourits, M., Normanno, N., Oaknin, A., Ojamaa, K., Papdimitriou, C., Penault-Llorca, F., Perrone, A.M., Pignata, S., Pikarsky, E., Rouleau, E., Rubio, M., Sapino, A., Schmalfeldt, B., Sehouli, J., Shapira, R., Steffensen, K.D., Sukhin, V., Syrios, J., Szallasi, Z., Taskiran, C., Terzic, M., Tischkowitz, M., Toth, I., Van de Vijver, K., Vardar, M.A., Wasag, B., Wimberger, P., Witteveen, E., Brenton, J.D., Ausems, M.G.E.M.
Publikováno v:
In Annals of Oncology March 2022 33(3):276-287
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
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
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
Autor:
te Paske, I.B.A.W., Garcia-Pelaez, J., Sommer, A.K., Matalonga, L., Starzynska, T., Jakubowska, A., Valle, L., Capella, G., Aretz, S., Holinski-Feder, E., Steinke-Lange, V., Laner, A., Schröck, E., Rump, A., Ligtenberg, M., Hoischen, A., Geverink, N., Evans, D.G., Tischkowitz, M., Laurie, S., van der Post, R.S., Lubinski, J., Oliveira, C., Hoogerbrugge, N., de Voer, R.M.
Publikováno v:
European Journal of Human Genetics, 29, 1354-1358
te Paske, I B A W, Garcia-Pelaez, J, Sommer, A K, Matalonga, L, Starzynska, T, Jakubowska, A, Valle, L, Capella, G, Aretz, S, Holinski-Feder, E, Steinke-Lange, V, Laner, A, Schröck, E, Rump, A, Ligtenberg, M, Hoischen, A, Geverink, N, Evans, D G, Tischkowitz, M, Laurie, S, van der Post, R S, Lubinski, J, Oliveira, C, Hoogerbrugge, N & de Voer, R M 2021, ' A mosaic PIK3CA variant in a young adult with diffuse gastric cancer: case report ', European Journal of Human Genetics, vol. 29, no. 9, pp. 1354-1358 . https://doi.org/10.1038/s41431-021-00853-6
European Journal of Human Genetics
European Journal of Human Genetics, 29, 9, pp. 1354-1358
te Paske, I B A W, Garcia-Pelaez, J, Sommer, A K, Matalonga, L, Starzynska, T, Jakubowska, A, Valle, L, Capella, G, Aretz, S, Holinski-Feder, E, Steinke-Lange, V, Laner, A, Schröck, E, Rump, A, Ligtenberg, M, Hoischen, A, Geverink, N, Evans, D G, Tischkowitz, M, Laurie, S, van der Post, R S, Lubinski, J, Oliveira, C, Hoogerbrugge, N & de Voer, R M 2021, ' A mosaic PIK3CA variant in a young adult with diffuse gastric cancer: case report ', European Journal of Human Genetics, vol. 29, no. 9, pp. 1354-1358 . https://doi.org/10.1038/s41431-021-00853-6
European Journal of Human Genetics
European Journal of Human Genetics, 29, 9, pp. 1354-1358
Hereditary diffuse gastric cancer (HDGC) is associated with germline deleterious variants in CDH1 and CTNNA1. The majority of HDGC-suspected patients are still genetically unresolved, raising the need for identification of novel HDGC predisposing gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b55c06ae4407fd0b60de07699ec8f63
https://www.repository.cam.ac.uk/handle/1810/328084
https://www.repository.cam.ac.uk/handle/1810/328084
Autor:
Steeghs, L., Gelderblom, H., Ho, V. K., Voorham, Q. J., Willems, S., Schuuring, E., Grunberg, K., Ligtenberg, M. J.
Publikováno v:
Virchows Archiv, 479(Suppl. 1). SPRINGER
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::77de73ea6dac1a3824dfdb165f5dc8ac
https://research.rug.nl/en/publications/2c817a25-2b8f-40dc-87de-5551e59be3e1
https://research.rug.nl/en/publications/2c817a25-2b8f-40dc-87de-5551e59be3e1
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
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)
Autor:
Pelaez J, Monteiro R, Lobo S, Sousa L, Pinheiro H, Castedo S, Garrido L, Teixeira M, Michils G, Bours V, de Putter R, Golmard L, Blanluet M, Colas C, Benusiglio P, Desseignes C, Florence C, Aretz S, Spier I, Huneburg R, Gieldon L, Schrock E, Holinski-Feder E, Steinke V, Calistri D, Tedaldi G, Ranzani G, Genuardi M, Silveira C, Silva I, Krajc M, Blatnik A, Novacovik S, Patino-Garcia A, Soto J, Lazaro C, Capella G, Brunet-Vidal J, Balmana J, Dominguez-Garrido E, Ligtenberg M, Fewings E, Fitzgerald R, Woodward E, Evans G, Hanson H, Lagerstedt-Robinson K, Bajalica-Lagercrantz S, Egas C, Tejada M, Dahan K, Feret D, Hoogerbrugge N, Tischkowitz M, Oliveira C
Publikováno v:
MEDICINE
r-FISABIO. Repositorio Institucional de Producción Científica
instname
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::209286cba8871551ab3179f3aeff12b9
https://fundanet.fisabio.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=12207
https://fundanet.fisabio.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=12207
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
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
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
http://europepmc.org/abstract/med/30302652