Zobrazeno 1 - 10
of 237
pro vyhledávání: '"Winter JP"'
Publikováno v:
Pediatric Infectious Diseases: Open Access.
Congenital malaria is a rare complication of Plasmodium infection during pregnancy. We present a case of a neonate with a mother who migrated from an endemic area. The mother developed fever during delivery due to Plasmodium vivax infection. Despite
Publikováno v:
Adolescence. Spring2005, Vol. 40 Issue 157, p103-113. 11p.
Autor:
Winter, JP, Joosten, Koen, IJland, MM, Verkade, HJ, Offringa, M (Martin), Dorrius, MD, van Hasselt, PM
Publikováno v:
Nederlands Tijdschrift voor Geneeskunde, 155:A936. Bohn Stafleu van Loghum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::e0364f4a5fa679efc4cbb4b6736c44e7
https://pure.eur.nl/en/publications/86e0d840-a7b5-43a1-bd9e-31fe937120cc
https://pure.eur.nl/en/publications/86e0d840-a7b5-43a1-bd9e-31fe937120cc
Autor:
WAISFISZ Q, MORGAN NV, SAVINO M, DE WINTER JP, VAN BERKEL CGM, IANZANO L, GIBSON RA, ARWERT F, MATHEW CG, PRONK JC, JOENJE H., SAVOIA, ANNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ede678939726a4fa2bd76ced95b33861
http://hdl.handle.net/11368/1701475
http://hdl.handle.net/11368/1701475
Autor:
Meyer, S, Tonnies, H, Fergusson, WF, Oostra, AB, Medhurst, AL, Waisfisz, Q, De Winter, JP, Chen, F, Carr, TF, Green, M, Barber, L, Eden, OB, Will, AM, Joenje, H, Taylor, GM
Publikováno v:
British Journal of Haematology, 129, 81-81. Wiley-Blackwell
Meyer, S, Tonnies, H, Fergusson, WF, Oostra, AB, Medhurst, AL, Waisfisz, Q, De Winter, JP, Chen, F, Carr, TF, Green, M, Barber, L, Eden, OB, Will, AM, Joenje, H & Taylor, GM 2005, ' Persistent chromosomal instability and cross-linker sensitivity in Fanconi anaemia derived leukaemia cell lines with bi-allelic FANCD1/BRCA2 mutations ', British Journal of Haematology, vol. 129, pp. 81-81 .
Meyer, S, Tonnies, H, Fergusson, WF, Oostra, AB, Medhurst, AL, Waisfisz, Q, De Winter, JP, Chen, F, Carr, TF, Green, M, Barber, L, Eden, OB, Will, AM, Joenje, H & Taylor, GM 2005, ' Persistent chromosomal instability and cross-linker sensitivity in Fanconi anaemia derived leukaemia cell lines with bi-allelic FANCD1/BRCA2 mutations ', British Journal of Haematology, vol. 129, pp. 81-81 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a3e4ec4443aa71d78e6f35e9cb35f0da
https://research.vumc.nl/en/publications/aed416ff-889f-4b6f-8ae7-eb0f518be986
https://research.vumc.nl/en/publications/aed416ff-889f-4b6f-8ae7-eb0f518be986
Autor:
Meyer, S, Fergusson, WD, Oostra, AB, Medhurst, AL, Waisfisz, Q, de Winter, JP, Chen, F, Carr, TF, Clayton-Smith, J, Clancy, T, Green, M, Barber, L, Eden, OB, Will, AM, Joenje, H, Taylor, GM
Publikováno v:
Meyer, S, Fergusson, WD, Oostra, AB, Medhurst, AL, Waisfisz, Q, de Winter, JP, Chen, F, Carr, TF, Clayton-Smith, J, Clancy, T, Green, M, Barber, L, Eden, OB, Will, AM, Joenje, H & Taylor, GM 2005, ' A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe Fanconi anemia and Biallelic FANCDI/BRCA2 mutations ', Genes, Chromosomes and Cancer, vol. 42, no. 4, pp. 404-415 . https://doi.org/10.1002/gcc.20153
Genes, Chromosomes and Cancer, 42(4), 404-415
Genes, Chromosomes and Cancer, 42(4), 404-415
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2687b26134ecdaeca36be9f663ead279
https://research.vumc.nl/en/publications/a58908b8-087e-4dcf-88ad-51552346f29b
https://research.vumc.nl/en/publications/a58908b8-087e-4dcf-88ad-51552346f29b
Autor:
Tischkowitz, M, Ameziane, N, Waisfisz, Q, De Winter, JP, Harris, R, Taniguchi, T, D'Andrea, A, Hodgson, SV, Mathew, CG, Joenje, H
Publikováno v:
British Journal of Haematology, 123(3), 469-471. Wiley-Blackwell
Tischkowitz, M, Ameziane, N, Waisfisz, Q, De Winter, JP, Harris, R, Taniguchi, T, D'Andrea, A, Hodgson, SV, Mathew, CG & Joenje, H 2003, ' Bi-allelic silencing of the Fanconi anaemia gene FANCF in acute myeloid leukaemia ', British Journal of Haematology, vol. 123, no. 3, pp. 469-471 . https://doi.org/10.1046/j.1365-2141.2003.04640.x
Tischkowitz, M, Ameziane, N, Waisfisz, Q, De Winter, JP, Harris, R, Taniguchi, T, D'Andrea, A, Hodgson, SV, Mathew, CG & Joenje, H 2003, ' Bi-allelic silencing of the Fanconi anaemia gene FANCF in acute myeloid leukaemia ', British Journal of Haematology, vol. 123, no. 3, pp. 469-471 . https://doi.org/10.1046/j.1365-2141.2003.04640.x
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9bee24f53f52079153a825723c92bd0d
https://research.vumc.nl/en/publications/11dae40b-711b-4bd9-9c22-140a6eb7ccf8
https://research.vumc.nl/en/publications/11dae40b-711b-4bd9-9c22-140a6eb7ccf8
Autor:
Xie, Y, de Winter, JP, Waisfisz, Q, Nieuwint, AWM, Scheper, RJ, Arwert, F, Hoatlin, ME, Ossenkoppele, GJ, Schuurhuis, GJ, Joenje, H
Publikováno v:
Xie, Y, de Winter, JP, Waisfisz, Q, Nieuwint, AWM, Scheper, RJ, Arwert, F, Hoatlin, ME, Ossenkoppele, GJ, Schuurhuis, GJ & Joenje, H 2000, ' Aberrant Fanconi anaemia protein profiles in acute myeloid leukaemia cells ', British Journal of Haematology, vol. 111, no. 4, pp. 1057-1064 .
British Journal of Haematology, 111(4), 1057-1064. Wiley-Blackwell
British Journal of Haematology, 111(4), 1057-1064. Wiley-Blackwell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::38e295947515a3a09bfea03f8f93a36e
https://research.vumc.nl/en/publications/0e1ad718-d0a1-494e-bcbf-0f898ff1c065
https://research.vumc.nl/en/publications/0e1ad718-d0a1-494e-bcbf-0f898ff1c065
Publikováno v:
Biometrics, 56, 808-814. Wiley-Blackwell Publishing Ltd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::a2327ffdb8d288a3638ee37278df7677
https://pure.eur.nl/en/publications/1af3e8d7-85d9-4471-b443-658b65821e07
https://pure.eur.nl/en/publications/1af3e8d7-85d9-4471-b443-658b65821e07
Autor:
Martin Digweed, Madeleine Carreau, Bender O, Jan C. Pronk, de Winter Jp, Quinten Waisfisz, van Berkel Cg, Fré Arwert, Detlev Schindler, Bosnoyan-Collins L, Holger Hoehn, Ilja Demuth, Martin A. Rooimans, Hans Joenje, Noa Alon, Manuel Buchwald
Publikováno v:
Nature Genetics, 20(3), 281-283. Nature Publishing Group
de Winter, JP, Waisfisz, Q, Rooimans, MA, van Berkel, CGM, Bosnoyan-Collins, L, Alon, N, Carreau, M, Bender, O, Demuth, I, Schindler, D, Pronk, JC, Arwert, F, Hoehn, H, Digweed, M, Buchwald, M & Joenje, H 1998, ' The Fanconi anaemia group G gene FANCG is identical with XRCC9 ', Nature Genetics, vol. 20, no. 3, pp. 281-283 . https://doi.org/10.1038/3093
de Winter, JP, Waisfisz, Q, Rooimans, MA, van Berkel, CGM, Bosnoyan-Collins, L, Alon, N, Carreau, M, Bender, O, Demuth, I, Schindler, D, Pronk, JC, Arwert, F, Hoehn, H, Digweed, M, Buchwald, M & Joenje, H 1998, ' The Fanconi anaemia group G gene FANCG is identical with XRCC9 ', Nature Genetics, vol. 20, no. 3, pp. 281-283 . https://doi.org/10.1038/3093
Fanconi anemia (FA) is an autosomal recessive disease with diverse clinical symptoms including developmental anomalies, bone marrow failure and early occurrence of malignancies1. In addition to spontaneous chromosome instability, FA cells exhibit cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c241ee99f4ade884358a7356eb185f5f
https://research.vumc.nl/en/publications/33c634b6-54b3-4a03-bac0-a0febcaa1485
https://research.vumc.nl/en/publications/33c634b6-54b3-4a03-bac0-a0febcaa1485