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Page 1
3-Hydroxy-3-methylglutaryl-CoA-lyase deficiency.
Ploechl E, Bachmann C, Colombo JP, Gibson KM. Ploechl E, et al. J Inherit Metab Dis. 1989;12(3):343. doi: 10.1007/BF01799236. J Inherit Metab Dis. 1989. PMID: 2515385 No abstract available.
Outcome of tyrosinaemia type III.
Ellaway CJ, Holme E, Standing S, Preece MA, Green A, Ploechl E, Ugarte M, Trefz FK, Leonard JV. Ellaway CJ, et al. Among authors: ploechl e. J Inherit Metab Dis. 2001 Dec;24(8):824-32. doi: 10.1023/a:1013936107064. J Inherit Metab Dis. 2001. PMID: 11916315
Late-onset ornithine transcarbamylase deficiency in two families with different mutations in the same codon.
Ploechl E, Ploechl W, Stoeckler-Ipsiroglu S, Pokorny H, Wermuth B. Ploechl E, et al. Clin Genet. 2001 Feb;59(2):111-4. doi: 10.1034/j.1399-0004.2001.590208.x. Clin Genet. 2001. PMID: 11260212
Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuria.
Tomoeda K, Awata H, Matsuura T, Matsuda I, Ploechl E, Milovac T, Boneh A, Scott CR, Danks DM, Endo F. Tomoeda K, et al. Among authors: ploechl e. Mol Genet Metab. 2000 Nov;71(3):506-10. doi: 10.1006/mgme.2000.3085. Mol Genet Metab. 2000. PMID: 11073718
Clinical experience with intravenous Augmentin in the treatment of paediatric infections.
Ploechl E, Huber EG. Ploechl E, et al. J Int Med Res. 1986;14(3):153-7. doi: 10.1177/030006058601400307. J Int Med Res. 1986. PMID: 3636248 Free article.