Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Anna E. Koopmans"'
Autor:
Emine Kilic, Anna E Koopmans, Koen A van Overdam, Ans M.W. van den Ouweland, Anass Hajjaj, Annelies de Klein, Rogier A. Oldenburg
Publikováno v:
Acta Ophthalmologica
Acta Ophthalmologica, 98(5), 464-471. Wiley-Blackwell Publishing Ltd
Acta Ophthalmologica, 98(5), 464-471. Wiley-Blackwell Publishing Ltd
Purpose Evaluation of phenotype and treatment outcome of retinal haemangioblastomas (RH) in von Hippel–Lindau (VHL) disease and correlation of these features with the genotype of VHL germline mutation carriers. Methods Retrospective analysis of a l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17cae56ef9728985a5e280e220dce4d2
https://doi.org/10.1111/aos.14360
https://doi.org/10.1111/aos.14360
Autor:
Jacobien Veenemans, Paul Milligan, Andrew M Prentice, Laura R A Schouten, Nienke Inja, Aafke C van der Heijden, Linsey C C de Boer, Esther J S Jansen, Anna E Koopmans, Wendy T M Enthoven, Rob J Kraaijenhagen, Ayse Y Demir, Donald R A Uges, Erasto V Mbugi, Huub F J Savelkoul, Hans Verhoef
Publikováno v:
PLoS Medicine, Vol 8, Iss 11, p e1001125 (2011)
It is uncertain to what extent oral supplementation with zinc can reduce episodes of malaria in endemic areas. Protection may depend on other nutrients. We measured the effect of supplementation with zinc and other nutrients on malaria rates.In a 2×
Externí odkaz:
https://doaj.org/article/8b0251caa43548018bb400522147a58e
Autor:
Robert M. Verdijk, Anna E Koopmans, Bert Eussen, Emine Kilic, Serdar Yavuzyigitoglu, Annelies de Klein, Alice van Bodegom, Dion Paridaens, Jolanda Vaarwater
Publikováno v:
Ophthalmology. 123:1118-1128
Purpose To investigate the prevalence and prognostic value of SF3B1 and EIF1AX mutations in uveal melanoma (UM) patients. Design Case series. Participants Cohort of 151 patients diagnosed with and treated for UM. Methods SF3B1 and EIF1AX mutations in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57f27bb0360bea1d29c4bc089cf3af31
https://doi.org/10.1016/j.ophtha.2016.01.023
https://doi.org/10.1016/j.ophtha.2016.01.023
Autor:
Robert M. Verdijk, Wilfred F. J. van IJcken, Thierry P P van den Bosch, Annelies de Klein, Nicole C. Naus, Christel E M Kockx, Rutger W W Brouwer, Dion Paridaens, Mark Nellist, Emine Kilic, Jolanda Vaarwater, Mike M P van den Berg, Anna E Koopmans
Publikováno v:
Modern Pathology, 27(10), 1321-1330. Nature Publishing Group
Uveal melanoma is a lethal cancer with a strong propensity to metastasize. Limited therapeutic options are available once the disease has disseminated. A strong predictor for metastasis is the loss of chromosome 3. Inactivating mutations in BAP1 enco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0437e2ee67891425b9e7d52ff99b3bec
https://doi.org/10.1038/modpathol.2014.43
https://doi.org/10.1038/modpathol.2014.43
Autor:
Anna E Koopmans, Erwin Brosens, Yolande van Bever, Annelies de Klein, Rene M. H. Wijnen, Dick Tibboel, Hanneke IJsselstijn, Mirjam Ploeg, Robbert J. Rottier
Publikováno v:
European Journal of Medical Genetics, 57(8), 440-452. Elsevier Masson
Esophageal Atresia (EA) is a severe developmental defect of the foregut that presents with or without a Tracheo-Esophageal Fistula (TEF). The prevalence of EA/TEF over time and around the world has been relatively stable. EA/TEF is manifested in a br
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6de1321f80987aca72a620f541b32b6c
https://doi.org/10.1016/j.ejmg.2014.05.009
https://doi.org/10.1016/j.ejmg.2014.05.009
Autor:
Anna E, Koopmans, Kimberley, Ober, Hendrikus J, Dubbink, Dion, Paridaens, Nicole C, Naus, Stephan, Belunek, Bart, Krist, Edward, Post, Ellen C, Zwarthoff, Annelies, de Klein, Robert M, Verdijk, Jolanda, Vaarwater
Publikováno v:
Investigative Ophthalmology & Visual Science, 55(9), 6024-6030. Association for Research in Vision and Ophthalmology Inc.
Purpose Hot-spot mutations in the promoter region of telomerase reverse transcriptase (TERT promoter mutations) occur frequently in cutaneous and conjunctival melanoma and are exceedingly rare in uveal melanoma. No information is available on the pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::762eeae50cd7c17cc29e056814182b15
https://doi.org/10.1167/iovs.14-14901
https://doi.org/10.1167/iovs.14-14901
Autor:
Robert M. Verdijk, Jackelien G.M. van Beek, Nicole C. Naus, Jolanda Vaarwater, Anna E Koopmans, Emine Kilic, Annelies de Klein
Publikováno v:
Melanoma Research, 25(5), 447-449. Lippincott Williams & Wilkins
Mutation of SF3B1 has been identified in low-grade uveal melanoma with a good prognosis. In this study, we compare chromosomal aberrations and gene mutations between a primary uveal melanoma and its multiple hepatic and peripancreatic metastases. DNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce068222fbc1ef18361b7082ec0695d0
https://doi.org/10.1097/CMR.0000000000000176
https://doi.org/10.1097/CMR.0000000000000176
Publikováno v:
British Journal of Cancer
British Journal of Cancer, 109(2), 493-496. Nature Publishing Group
British Journal of Cancer, 109(2), 493-496. Nature Publishing Group
Background: Mutations in GNAQ and GNA11, encoding the oncogenic G-protein alpha subunit q and 11, respectively, occur frequently in the majority of uveal melanomas. Methods: Exons 4 and 5 from GNAQ and GNA11 were amplified and sequenced from 92 cilia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c54164712e427cc6accc9bcfca698d3a
http://europepmc.org/articles/PMC3721402
http://europepmc.org/articles/PMC3721402
Autor:
Anna E Koopmans, Jolanda Vaarwater, Kyra N Smit, Emine Kilic, Natasha M. van Poppelen, Dion Paridaens, Bert Eussen, Job van Riet, Annelies de Klein, Tom Brands, Berna Beverloo, Hendrikus J. Dubbink, Wojtek Drabarek, Robert M. Verdijk, Harmen J.G. van de Werken, Nicole C. Naus, Serdar Yavuzyigitoglu
Publikováno v:
Ophthalmology. 124(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab5332fe15ea8ff2f2e5cced3f4f3378
https://pubmed.ncbi.nlm.nih.gov/27916271
https://pubmed.ncbi.nlm.nih.gov/27916271
Autor:
Serdar, Yavuzyigitoglu, Anna E, Koopmans, Robert M, Verdijk, Jolanda, Vaarwater, Bert, Eussen, Alice, van Bodegom, Dion, Paridaens, Emine, Kiliç, Annelies, de Klein
Publikováno v:
Ophthalmology. 123(5)
To investigate the prevalence and prognostic value of SF3B1 and EIF1AX mutations in uveal melanoma (UM) patients.Case series.Cohort of 151 patients diagnosed with and treated for UM.SF3B1 and EIF1AX mutations in primary tumors were investigated using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4e4a65dfb6a51d3e40f431134b8a4f6f
https://pubmed.ncbi.nlm.nih.gov/26923342
https://pubmed.ncbi.nlm.nih.gov/26923342