Zobrazeno 1 - 10
of 234
pro vyhledávání: '"Meijers-Heijboer, E. J."'
Autor:
Lakeman, P., van Koningsbruggen, S., Redeker, E. J. W., Ottenheim, C. P. E., Mathijssen, I. B., Cornel, M. C., Mannens, M. M. A. M., Meijers-Heijboer, E. J., Henneman, L.
Publikováno v:
Lakeman, P, van Koningsbruggen, S, Redeker, E J W, Ottenheim, C P E, Mathijssen, I B, Cornel, M C, Mannens, M M A M, Meijers-Heijboer, E J & Henneman, L 2018, ' Evaluation of an expanded carrier screening offer in a non commercial setting ', European Journal of Human Genetics, vol. 26, pp. 82-83 .
European Journal of Human Genetics, 26, 82-83. Nature Publishing Group
European Journal of Human Genetics, 26, 82-83. Nature Publishing Group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5140b6936c4ce0fe0716b249fcc087f8
https://research.vumc.nl/en/publications/d7fe362b-7558-488e-a9c9-bcb58ad0e444
https://research.vumc.nl/en/publications/d7fe362b-7558-488e-a9c9-bcb58ad0e444
Autor:
Meijers-Heijboer, E J, Verhoog, L C, Brekelmans, C T M, Seynaeve, C, Tilanus-Linthorst, M M A, Wagner, A, Dukel, L, Devilee, P, van den Ouweland, A M W, van Geel, A N, Klijn, J G M, Brekelmans, C T (AUTHOR), Tilanus-Linthorst, M M (AUTHOR), van den Ouweland, A M (AUTHOR), Klijn, J G (AUTHOR)
Publikováno v:
Lancet. 6/10/2000, Vol. 355 Issue 9220, p2015-2020. 6p. 3 Charts, 3 Graphs.
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
Autor:
Zwijnenburg, P. J. G., Deurloo, K. L., Waterham, H. R., Meijers-Heijboer, E. J., van Vugt, J. M. G., Tan-Sindhunata, M. B.
Publikováno v:
Prenatal Diagnosis, 30(2), 162-164. John Wiley and Sons Ltd
Zwijnenburg, P J G, Deurloo, K L, Waterham, H R, Meijers-Heijboer, E J, van Vugt, J M G & Sindhunata, M B 2010, ' Second trimester prenatal diagnosis of rhizomelic chondrodysplasia punctata type 1 on ultrasound findings ', Prenatal Diagnosis, vol. 30, no. 2, pp. 162-164 . https://doi.org/10.1002/pd.2425
Prenatal diagnosis, 30(2), 162-164. John Wiley and Sons Ltd
Zwijnenburg, P J G, Deurloo, K L, Waterham, H R, Meijers-Heijboer, E J, van Vugt, J M G & Sindhunata, M B 2010, ' Second trimester prenatal diagnosis of rhizomelic chondrodysplasia punctata type 1 on ultrasound findings ', Prenatal Diagnosis, vol. 30, no. 2, pp. 162-164 . https://doi.org/10.1002/pd.2425
Prenatal diagnosis, 30(2), 162-164. John Wiley and Sons Ltd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1f433e4ee2aac81315cc63300f2745b8
https://research.vumc.nl/en/publications/c33cada0-85d4-44ab-ad5e-83837da40100
https://research.vumc.nl/en/publications/c33cada0-85d4-44ab-ad5e-83837da40100
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Menke-Pluymers, M. B. E., Seynaeve, C., van Geel, A. N., Klijn, J. G. M., Meijers-Heijboer, E. J., Eggermont, A. M. M.
Publikováno v:
Nederlands tijdschrift voor geneeskunde, 149(48), 2663-2667. Bohn Stafleu van Loghum
Preventive surgical procedures for inherited risk of breast cancer Forwomen with a demonstrated BRCA1 or BRCA2 mutation, the cumulative risk of developing invasive breast cancer before the age of 70 years is about 50-85% and the risk of developing in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::853e5b7aaf6753feb335ff6c420dad8d
https://pure.amc.nl/en/publications/preventief-chirurgisch-ingrijpen-bij-erfelijke-belasting-voor-borstkanker(c020bea3-9b6b-43a4-9fbd-8f37341a1ce4).html
https://pure.amc.nl/en/publications/preventief-chirurgisch-ingrijpen-bij-erfelijke-belasting-voor-borstkanker(c020bea3-9b6b-43a4-9fbd-8f37341a1ce4).html
Autor:
Meijers-Heijboer, E. J., Verhoog, L. C., Brekelmans, C. T. M., Seynaeve, C., Tilanus-Linthorst, M. M. A., Wagner, A., Dukel, L., Devilee, P., van den Ouweland, A. M. W., van Geel, A. N., Klijn, J. G. M.
Publikováno v:
GYNAKOLOGE, 33(10), 768-769. Springer Verlag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::49d11881560ac41b5609f0bb6ce41e1e
https://pure.amc.nl/en/publications/genetic-testing-and-prophylactic-surgery-in-familiar-clusters-of-brca1-or-brca2-mutation(61d4e9bf-849c-4769-adcd-8c6b49abcb19).html
https://pure.amc.nl/en/publications/genetic-testing-and-prophylactic-surgery-in-familiar-clusters-of-brca1-or-brca2-mutation(61d4e9bf-849c-4769-adcd-8c6b49abcb19).html
Autor:
Verhoog, L. C., Berns, E. M., Brekelmans, C. T., Seynaeve, C., Meijers-Heijboer, E. J., Klijn, J. G.
Publikováno v:
Journal of clinical oncology, 18(21 Suppl), 119S-124S. American Society of Clinical Oncology
Breast cancer in BRCA2 gene mutation carriers differs from BRCA1-associated breast cancer or so-called sporadic breast cancer in clinical features and behavior. These differences may be of importance for the prevention, screening, and ultimately trea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::df0f70edc38debf7f9f7149888e2ab68
https://pure.amc.nl/en/publications/prognostic-significance-of-germline-brca2-mutations-in-hereditary-breast-cancer-patients(3dfda171-60af-460c-82d5-c919f342a1f8).html
https://pure.amc.nl/en/publications/prognostic-significance-of-germline-brca2-mutations-in-hereditary-breast-cancer-patients(3dfda171-60af-460c-82d5-c919f342a1f8).html
Autor:
Lodder, L. N., Frets, P. G., Trijsburg, R. W., Meijers-Heijboer, E. J., Klijn, J. G., Duivenvoorden, H. J., Tibben, A., Wagner, A., van der Meer, C. A., Devilee, P., Cornelisse, C. J., Niermeijer, M. F.
Publikováno v:
Journal of medical genetics, 36(12), 906-913. BMJ Publishing Group
Presymptomatic DNA testing for autosomal dominant hereditary breast/ovarian cancer (HBOC) became an option after the identification of the BRCA1 and BRCA2 genes in 1994-1995. Healthy female mutation carriers have a high lifetime risk for breast cance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::c2961be7bdf92b740aefb9fd53c81ba3
https://pure.amc.nl/en/publications/presymptomatic-testing-for-brca1-and-brca2-how-distressing-are-the-pretest-weeks-rotterdamleiden-genetics-working-group(6f7fc7c0-40e5-4f9e-b280-16a5fc4dd517).html
https://pure.amc.nl/en/publications/presymptomatic-testing-for-brca1-and-brca2-how-distressing-are-the-pretest-weeks-rotterdamleiden-genetics-working-group(6f7fc7c0-40e5-4f9e-b280-16a5fc4dd517).html
Autor:
Dudok-de Wit, A. C., Tibben, A., Duivenvoorden, H. J., Niermeijer, M. F., Passchier, J., Trijsburg, R. W., Lindhout, D., Meijers-Heijboer, E. J., Frets, P. G., Lodder, L. N., Zoetewij, M. W., Klijn, J. G. M., Brocker-Vriends, A., van Haeringen, A., Helderman, A. T. J. M., Hilhorst-Hofstee, Y., Kant, S., Maat-Kievit, J. A., Oosterwijk, J. C., van der Smagt, J. J., Vegter-van der Vlis, M., Vries-van der Weerd, M. A. C. S., Zoeteweij, M. W., Bakker, E., Devilee, P., Losekoot, M., Tops, C., Cornelisse, C. J., Vasen, H. F. A.
Publikováno v:
American Journal of Medical Genetics, 75, 62-74. Wiley-Liss Inc.
American journal of medical genetics, 75(1), 62-74. Wiley-Liss Inc.
American journal of medical genetics, 75(1), 62-74. Wiley-Liss Inc.
In 50% risk carriers for Huntington disease (n = 41), hereditary cerebral hemorrhage with amyloidosis Dutch-type (n = 9) familial adenomatous polyposis coli (n = 45) and hereditary breast and ovarian cancer (n = 24), pretest intrusion and avoidance (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52df4e5fa6479e9885bb2d3e2c818148
https://pure.eur.nl/en/publications/d2fcc5d3-bf67-4a14-9ffd-752793c90a45
https://pure.eur.nl/en/publications/d2fcc5d3-bf67-4a14-9ffd-752793c90a45