Zobrazeno 1 - 4
of 4
pro vyhledávání: '"M. E. J. Den Boer"'
Autor:
G. Biesbroek, B. Kapitein, I. M. Kuipers, M. P. Gruppen, D. van Stijn, T. E. Peros, M. van Veenendaal, M. H. A. Jansen, C. W. van der Zee, M. van der Kuip, E. G. J. von Asmuth, M. G. Mooij, M. E. J. den Boer, G. W. Landman, M. A. van Houten, D. Schonenberg-Meinema, A. M. Tutu van Furth, M. Boele van Hensbroek, H. Scherpbier, K. E. van Meijgaarden, T. H. M. Ottenhoff, S. A. Joosten, N. Ketharanathan, M. Blink, C. L. H. Brackel, H. L. Zaaijer, P. Hombrink, J. M. van den Berg, E. P. Buddingh, T. W. Kuijpers
Publikováno v:
PLoS ONE, Vol 17, Iss 11 (2022)
Multisystem Inflammatory Syndrome in Children (MIS-C) is a severe inflammatory disease in children related to SARS-CoV-2 with multisystem involvement including marked cardiac dysfunction and clinical symptoms that can resemble Kawasaki Disease (KD).
Externí odkaz:
https://doaj.org/article/bd19edd075cc4cb4b502afca445c9184
Autor:
Lodewijk IJlst, Frits A. Wijburg, R. J. A. Wanders, M. A. Van Werkhoven, Hugo S. A. Heymans, M. E. J. Den Boer, M.G. van Pampus, W. Oostheim
Publikováno v:
Pediatric research, 48(2), 151-154. Lippincott Williams and Wilkins
Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency is an autosomal recessive disorder of mitochondrial fatty acid oxidation. Apart from life-threatening metabolic derangement with hypoketotic hypoglycemia, patients often show liver disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76bba2753979d5a50cb6262105b3da96
https://doi.org/10.1203/00006450-200008000-00006
https://doi.org/10.1203/00006450-200008000-00006
Autor:
P. Vreken, M. E. J. den Boer, A. H. van Gennip, Frits A. Wijburg, L. IJlst, Ronald J.A. Wanders
Publikováno v:
Journal of inherited metabolic disease, 22(4), 442-487. Springer Netherlands
In recent years tremendous progress has been made with respect to the enzymology of the mitochondrial fatty acid beta-oxidation machinery and defects therein. Firstly, a number of new mitochondrial beta-oxidation enzymes have been identified, includi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55d69498989652b8fb75f52009a8dbbb
https://doi.org/10.1023/a:1005504223140
https://doi.org/10.1023/a:1005504223140
Autor:
R. J. A. Wanders, Nadia A. Oey, Jos P.N. Ruiter, Hans R. Waterham, Kees Boer, Marinus Duran, J.A.M. van der Post, Frits A. Wijburg, M. E. J. Den Boer
Publikováno v:
Journal of inherited metabolic disease, 26(4), 385-392. Springer Netherlands
As the human fetus and placenta are considered to be primarily dependent on glucose oxidation for energy metabolism, the cause of the remarkable association between severe maternal pregnancy complications and the carriage of a fetus with an inborn er
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0505cad97b8418365743ed38c6bca33
https://pubmed.ncbi.nlm.nih.gov/12971426
https://pubmed.ncbi.nlm.nih.gov/12971426