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NADH:Q1 oxidoreductase deficiency without lactic acidosis in a patient with Leigh syndrome: implications for the diagnosis of inborn errors of the respiratory chain.
Wijburg FA, Wanders RJ, van Lie Peters EM, Vos GD, Loggers HG, Bolhuis PA, Herzberg NH, Ruitenbeek W, van Wilsem A, ten Houten R, et al. Wijburg FA, et al. Among authors: vos gd. J Inherit Metab Dis. 1991;14(3):297-300. doi: 10.1007/BF01811686. J Inherit Metab Dis. 1991. PMID: 1770777 No abstract available.
Vanishing spleen after Nissen fundoplication: a case report.
Dijkman KP, van Heurn LW, Leroy PL, Vos GD. Dijkman KP, et al. Among authors: vos gd. Eur J Pediatr. 2009 Mar;168(3):355-7. doi: 10.1007/s00431-008-0752-8. Epub 2008 Jul 3. Eur J Pediatr. 2009. PMID: 18597115
44 results