Zobrazeno 1 - 4
of 4
pro vyhledávání: '"G. W. Ten Tusscher"'
Publikováno v:
Clinical Case Reports, Vol 10, Iss 6, Pp n/a-n/a (2022)
Abstract Systemic juvenile idiopathic arthritis (sJIA, also called Still's disease) is a rare childhood auto‐inflammatory disease with significant morbidity. This case report illustrates the clinical course and highlights diagnostic challenges. FDG
Externí odkaz:
https://doaj.org/article/124c637cffc749008e20eaead079e203
Autor:
Lies Hulshof, Saskia A. Overbeek, Anne L. Wyllie, Mei Ling J. N. Chu, Debby Bogaert, Wilco de Jager, Leon M. J. Knippels, Elisabeth A. M. Sanders, Wim M. C. van Aalderen, Johan Garssen, Belinda van’t Land, Aline B. Sprikkelman, The Clinical Study Group, A. Blauw, B. Dontje, Y. C. M. Duijvestein, W. H. C. de Boom, I. Groot, M. Boks, Y. van Kooyk, D. H. H. Fandri, D. Hijnen, M. A. Middelkamp-Hup, B. Papi, M. Roelofs, A. Rijnierse, D. Veening, Clinical Trial Support, B. J. Prakken, G. W. Ten Tusscher, R. A. Tupker, L. E. M. Willemsen
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
BackgroundAtopic dermatitis (AD) is the most common chronic inflammatory skin disease in infancy with a complex pathology. In adults, the clinical severity of AD has been associated with increases in T helper cell type (Th) 2, Th22, and Th17 serum ma
Externí odkaz:
https://doaj.org/article/2ac28a6b276d42c296dde81fb54acb95
Autor:
G W, ten Tusscher, J, de Weerdt, C M, Roos, R W, Griffioen, F H, De Jongh, M, Westra, J W, van der Slikke, J, Oosting, K, Olie, J G, Koppe
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 90(11)
Perinatal exposure to Dutch background dioxin levels is rather high. Studies of calamities have shown that dioxins negatively influence the respiratory system. It was hypothesized that perinatal exposure to background dioxin levels leads to lung subo
Publikováno v:
Biomedical chromatography : BMC. 13(4)
In this study the validation of a reversed-phase high-performance liquid chromatography (HPLC) method, with UV-detection, for both caffeine and paraxanthine in human serum is described. This method is feasible for cytochrome P450 1A2 (CYP1A2) phenoty