المؤلفون: Tischkowitz, M, Colas, C, Pouwels, S, Hoogerbrugge, N, Ligtenberg, M, Oostenbrink, Rianne, Sijmons, R, Evans, G, Woodward, E, Peltonen, S, Hietala, M

المساهمون: Pediatrics

المصدر: 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/s41431-020-0651-7Test
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

مصطلحات موضوعية: PTEN, medicine.medical_specialty, Colorectal cancer, Consensus Development Conferences as Topic, Vascular damage Radboud Institute for Health Sciences [Radboudumc 16], Population, MEDLINE, CHILDREN, Article, 03 medical and health sciences, 0302 clinical medicine, SDG 3 - Good Health and Well-being, Medicine and Health Sciences, Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14], Genetics, Humans, Medicine, Genetic Testing, education, Intensive care medicine, Cancer genetics, Early Detection of Cancer, Genetics (clinical), 030304 developmental biology, Preventive medicine, 0303 health sciences, education.field_of_study, biology, business.industry, Endometrial cancer, Cancer, Guideline, medicine.disease, RISKS, Women's cancers Radboud Institute for Health Sciences [Radboudumc 17], 030220 oncology & carcinogenesis, Practice Guidelines as Topic, biology.protein, Medical genetics, Hamartoma Syndrome, Multiple, business

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الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0ca7f01c9a5953a5a2debf53d05dbf4Test
https://doi.org/10.1038/s41431-020-0651-7Test

المؤلفون: 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.

المساهمون: 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.

المصدر: 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.33214Test

مصطلحات موضوعية: Male, Adult, Oncology, Cancer Research, 2019-20 coronavirus outbreak, medicine.medical_specialty, sarcoma, Databases, Factual, Coronavirus disease 2019 (COVID-19), Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), Sarcoma/diagnosis, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Humans, Medicine, Aged, business.industry, Sarcoma, Syndrome, Middle Aged, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Lynch syndrome, MSH2, 030220 oncology & carcinogenesis, Colorectal Neoplasms, Hereditary Nonpolyposis/diagnosis, Female, 030211 gastroenterology & hepatology, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::256db311728c9b8d2ebfdfd70b7043e2Test
https://doi.org/10.1002/ijc.33214Test

المؤلفون: 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

المساهمون: Guided Treatment in Optimal Selected Cancer Patients (GUTS), Erasmus School of Health Policy & Management, Pediatrics, Legius, Eric

المصدر: 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/s10689-018-0110-6Test
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

مصطلحات موضوعية: 0301 basic medicine, Cancer Research, Pediatrics, Databases, Factual, Colorectal cancer, International Cooperation, 030105 genetics & heredity, Medical Oncology, GUIDELINES, COLORECTAL-CANCER, Tumours of the digestive tract Radboud Institute for Health Sciences [Radboudumc 14], 0302 clinical medicine, Epidemiology, Medicine and Health Sciences, Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14], Registries, Genetics (clinical), Syndrome, Quality Improvement, Women's cancers Radboud Institute for Health Sciences [Radboudumc 17], Rare diseases, Europe, Oncology, 030220 oncology & carcinogenesis, Clinical Competence, Hereditary diffuse gastric cancer, medicine.medical_specialty, Short Communication, European Reference Network, behavioral disciplines and activities, Time-to-Treatment, 03 medical and health sciences, All institutes and research themes of the Radboud University Medical Center, Cross border health care, SDG 3 - Good Health and Well-being, Genetic, Neoplastic Syndromes, Hereditary, Genetics, medicine, Genetic predisposition, Humans, Genetic Predisposition to Disease, Genetic Testing, Neurofibromatosis, Information Services, business.industry, Information Dissemination, Remote Consultation, Cancer, medicine.disease, PREVENTION, Hereditary cancer, Li–Fraumeni syndrome, business, Rare disease

وصف الملف: application/pdf; Print

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee01440d9c450a349db2b80095a24994Test
http://europepmc.org/abstract/med/30302652Test

المؤلفون: Bruin, J. H. F. M., Kievit, W., Ligtenberg, M. J. L., Nagengast, F. M., Adang, E. M. M., Ruers, T. J., Kleibeuker, J. H., Sijmons, R. H., Krieken, J. H. J. M., nicoline hoogerbrugge

المصدر: Nederlands Tijdschrift voor Geneeskunde, 149, 1792-8
Nederlands Tijdschrift voor Geneeskunde, 149, 32, pp. 1792-8
ResearcherID

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Age-related aspects of cancer [ONCOL 2], Genetics and epigenetic pathways of disease [NCMLS 6], Hereditary cancer and cancer-related syndromes [ONCOL 1], Effective Hospital Care [EBP 2], nutritional and metabolic diseases, Aetiology, screening and detection [ONCOL 5], digestive system diseases, Quality of Care [ONCOL 4], Genomic disorders and inherited multi-system disorders [IGMD 3], Molecular epidemiology [NCEBP 1], Evaluation of complex medical interventions [NCEBP 2], Immune Regulation [NCMLS 2], Translational research [ONCOL 3], Molecular gastro-enterology and hepatology [IGMD 2], neoplasms, Molecular diagnosis, prognosis and monitoring [UMCN 1.2]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::92cec58bb841fe884df0411dd424d9b4Test
http://hdl.handle.net/2066/48109Test

المؤلفون: Peelen, T., Vanvliet, M., Petrijbosch, A., Mieremet, R., Szabo, C., Vandenouweland, A. M. W., Hogervorst, F., Brohet, R., Ligtenberg, M. J. L., Teugels, E., Vanderluijt, R., Vanderhout, A. H., Gille, J. J. P., Pals, G., Jedema, I., Olmer, R., Vanleeuwen, I., Newman, B., Plandsoen, M., Vanderest, M., Brink, G., Hageman, S., Arts, P. J. W., Bakker, M. M., Willems, H. W., Vanderlooij, E., Neyns, B., Bonduelle, M., Jansen, R., Oosterwijk, J. C., Sijmons, R., Smeets, H. J. M., Vanasperen, C. J., Meijersheijboer, H., Klijn, J. G. M., Degreve, J., King, M. C., Menko, F. H., Brunner, H. G., Halley, D., Vanommen, G. J. B., Vasen, H. F. A., Cornelisse, C. J., Vantveer, L. J., Peter de Knijff, Bakker, E., Devilee, P.

المساهمون: Clinical Genetics, Pathology, Medical Oncology, Damage and Repair in Cancer Development and Cancer Treatment (DARE), Guided Treatment in Optimal Selected Cancer Patients (GUTS), Targeted Gynaecologic Oncology (TARGON), Other departments

المصدر: American Journal of Human Genetics, 60, 5, pp. 1041-1049
American Journal of Human Genetics, 60, 1041-1049
ResearcherID
American Journal of Human Genetics, 60, 1041-1049. Cell Press
American Journal of Human Genetics, 60(5), 1041-1049. CELL PRESS
Scopus-Elsevier
American journal of human genetics, 60(5), 1041-1049. Cell Press

مصطلحات موضوعية: RAPID DETECTION, GERMLINE MUTATIONS, DNA, Original Articles, Tumor pathologie, FREQUENCY, CARRIERS, PROTEIN TRUNCATION TEST, SUSCEPTIBILITY GENE, SDG 3 - Good Health and Well-being, LINKAGE, De rol van chromosoomafwijkingen en (anti-)oncogenen in humane tumoren, The role of chromosomal aberrations and (anti-)oncogenes in human tumours, Tumor pathology, 185DELAG, GeneralLiterature_REFERENCE(e.g.,dictionaries,encyclopedias,glossaries)

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::87641196e488ad33abf5c4bfbb9eeac8Test
https://hdl.handle.net/2066/25573Test

المؤلفون: Møller P, Toni Seppälä, Bernstein I, Holinski-Feder E, Sala P, Dg, Evans, Lindblom A, Macrae F, Blanco I, Sijmons R, Jeffries J, Vasen H, Burn J, Nakken S, Hovig E, Ea, Rødland, Tharmaratnam K, Wh, Vos Tot Nederveen Cappel, Hill J, Wijnen J

المصدر: Europe PubMed Central

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4373f3ff2602ed51c871bab081318cd6Test
http://europepmc.org/abstract/med/26657901Test