Zobrazeno 1 - 10
of 311
pro vyhledávání: '"Duivenvoorden, H J."'
Autor:
Jochems, E. C.1,2 e.c.jochems@gmail.com, Duivenvoorden, H. J.3, van Dam, A.4,5, Mulder, C. L.1,6, van der Feltz-Cornelis, C. M.4,7
Publikováno v:
Motivation & Emotion. Dec2018, Vol. 42 Issue 6, p816-830. 15p.
Autor:
van Dooren, S.1,2 s.vandooren@erasmusmc.nl, Duivenvoorden, H. J.1, Passchier, J.1, Bannink, M.3, Tan, M. B. M.3,4, Oldenmenger, W. H.2, Seynaeve, C.2,4, van der Rijt, C. C. D.2
Publikováno v:
Psycho-Oncology. Oct2009, Vol. 18 Issue 10, p1080-1087. 8p. 4 Charts, 1 Graph.
Akademický článek
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Akademický článek
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Autor:
Braat, J. P. M., Mulder, P. G., Duivenvoorden, H. J., Gerth van Wijk, R., Rijntjes, E., Fokkens, W. J.
Publikováno v:
Clinical and experimental allergy, 32(5), 690-697. Wiley-Blackwell
BACKGROUND: Epidemiological studies in the past have focused on meteorological conditions, pollution and pollen and their relationship with symptoms of bronchial hyper-reactivity, however, there are no epidemiological studies which examine a wide ran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::5cfd322545cbe8c6e8e05793893d2dda
https://pure.amc.nl/en/publications/pollutional-and-meteorological-factors-are-closely-related-to-complaints-of-nonallergic-noninfectious-perennial-rhinitis-patients-a-time-series-model(1c02c7d3-9693-411d-bb06-71618d7deeab).html
https://pure.amc.nl/en/publications/pollutional-and-meteorological-factors-are-closely-related-to-complaints-of-nonallergic-noninfectious-perennial-rhinitis-patients-a-time-series-model(1c02c7d3-9693-411d-bb06-71618d7deeab).html
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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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
Publikováno v:
Journal of Medical Genetics, 35, 745-754. BMJ Publishing Group
JOURNAL OF MEDICAL GENETICS, 35(9), 745-754. BMJ PUBLISHING GROUP
JOURNAL OF MEDICAL GENETICS, 35(9), 745-754. BMJ PUBLISHING GROUP
The first comparative study on predicting post-test distress (conceptualised by intrusion and avoidance, measured with the Impact of Event Scale) after presymptomatic genetic testing for Huntington's disease (HD, n = 25), cancer syndromes (familial a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::bfbe6bdd48abf82906d59df227791ada
https://pure.eur.nl/en/publications/0a2e969c-fe4c-4976-a98e-b4e06e0db778
https://pure.eur.nl/en/publications/0a2e969c-fe4c-4976-a98e-b4e06e0db778
Autor:
de Vries, B B, van den Ouweland, A M, Mohkamsing, S, Duivenvoorden, H J, Mol, E, Gelsema, K, van Rijn, M, Halley, D J, Sandkuijl, L A, Oostra, B A, Tibben, A, Niermeijer, M F
The fragile X syndrome is an X-linked mental retardation disorder caused by an expanded CGG repeat in the first exon of the fragile X mental retardation (FMR1) gene. Its frequency, X-linked inheritance, and consequences for relatives all prompt for d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6765f5e57e4b28be14932a04874417d5
https://europepmc.org/articles/PMC1715962/
https://europepmc.org/articles/PMC1715962/