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of 2
pro vyhledávání: '"I M W, van Hoogstraten"'
Autor:
B A C Dijkmans, Paul Lips, A E Voskuyl, H G Raterman, Marco W.J. Schreurs, V P van Halm, Suat Simsek, Marjolein Peters, I M W van Hoogstraten, Michael T. Nurmohamed, W.F. Lems
Publikováno v:
Raterman, H G, Voskuyl, A E, Simsek, S, Schreurs, M W J, van Hoogstraten, I M W, Peters, M J L, van Halm, V P, Dijkmans, B A C, Lips, P, Lems, W F & Nurmohamed, M T 2013, ' Increased progression of carotid intima media thickness in thyroid peroxidase antibodies-positive rheumatoid arthritis patients ', European Journal of Endocrinology, vol. 169, no. 6, pp. 751-757 . https://doi.org/10.1530/EJE-13-0394
European journal of endocrinology / European Federation of Endocrine Societies, 169(6), 751-757. BioScientifica Ltd.
European Journal of Endocrinology, 169(6), 751-757. Bioscientifica Ltd
European Journal of Endocrinology, 169(6), 751-757. BioScientifica Ltd.
European journal of endocrinology / European Federation of Endocrine Societies, 169(6), 751-757. BioScientifica Ltd.
European Journal of Endocrinology, 169(6), 751-757. Bioscientifica Ltd
European Journal of Endocrinology, 169(6), 751-757. BioScientifica Ltd.
ObjectiveAutoimmune diseases such as rheumatoid arthritis (RA) and hypothyroidism tend to cluster, and this coexistence amplifies the elevated cardiovascular risk in RA. Whether thyroid peroxidase antibodies (TPOabs) are associated with increased car
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d08216dfbc559dfe77559cf310191e7
https://hdl.handle.net/1871.1/20929522-55e8-4caa-8c36-0c520843ab25
https://hdl.handle.net/1871.1/20929522-55e8-4caa-8c36-0c520843ab25
Autor:
C E, Hogen Esch, G D S, Csizmadia, I M W, van Hoogstraten, M W J, Schreurs, M L, Mearin, B M E, von Blomberg
Publikováno v:
Alimentary pharmacologytherapeutics. 31(7)
In 1997-1998, 6127 asymptomatic children aged 2-4 years were screened for coeliac disease (CD) by anti-endomysium (EmA) testing in the Netherlands. After 6 (+/-2) months, biopsies were performed in 57 seropositive children; 31(54%) had villous atroph