Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Bonten, E J"'
Autor:
Bakker, E, Veenema, H, Den Dunnen, J T, van Broeckhoven, C, Grootscholten, P M, Bonten, E J, van Ommen, G J, Pearson, P L
Publikováno v:
Journal of Medical Genetics; Sep1989, Vol. 26 Issue 9, p553-559, 7p, 6 Diagrams, 2 Charts
Autor:
Bakker, E, Bonten, E J, De Lange, L F, Veenema, H, Majoor-Krakauer, D, Hofker, M H, Van Ommen, G J, Pearson, P L
Publikováno v:
Journal of Medical Genetics; Dec1986, Vol. 23 Issue 6, p573-580, 8p
Autor:
Bakker, E., Bonten, E. J., Veenema, H., Dunnen, J. T., Grootscholten, P. M., Ommen, G. J. B., Pearson, P. L.
Publikováno v:
Journal of Inherited Metabolic Disease; March 1989, Vol. 12 Issue: Supplement 1 p174-190, 17p
Publikováno v:
Journal of Biological Chemistry; November 1995, Vol. 270 Issue: 44 p26441-5, 5p
Autor:
Bakker, E., Broeckhoven, Ch. Van, Bonten, E. J., van de Vooren, M. J., Veenema, H., Hul, W. Van, Ommen, G. J. B. Van, Vandenberghe, A., Pearson, P. L.
Publikováno v:
Nature; 10/8/1987, Vol. 329 Issue 6139, p554-556, 3p
Autor:
Tai, H. -L, Michael Fessing, Bonten, E. J., Yanishevsky, Y., D Azzo, A., Krynetski, E. Y., Evans, W. E.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4689caae940e665ce892e6e0840bd938
http://www.scopus.com/inward/record.url?eid=2-s2.0-0032693405&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0032693405&partnerID=MN8TOARS
Autor:
Chiara Caletti, Davide Selvestrel, Marianna Lucafò, Simona Granata, Gabriele Stocco, Eva Cuzzoni, Erik J. Bonten, Giovanni Montini, Robert McCorkle, Chan Zou, William E. Evans, Giuliana Decorti, Andrea Pasini, Alessio Cozzarolo, Giovanni Gambaro, Gianluigi Zaza
Publikováno v:
Clinical and Translational Science, Vol 14, Iss 3, Pp 964-975 (2021)
Clinical and Translational Science
Clinical and Translational Science
To assess whether NLRP3 gene promoter methylation was able to discriminate glucocorticoid (GC)-resistant from GC-sensitive idiopathic nephrotic syndrome (INS), patients with minimal change disease (MCD) or focal segmental glomerulosclerosis (FSGS), w
Autor:
Tai HL; St Jude Children's Research Hospital and University of Tennessee, Memphis 38105, USA., Fessing MY, Bonten EJ, Yanishevsky Y, d'Azzo A, Krynetski EY, Evans WE
Publikováno v:
Pharmacogenetics [Pharmacogenetics] 1999 Oct; Vol. 9 (5), pp. 641-50.