Automated turbidimetric benzalkonium chloride method for measurement of protein in urine and cerebrospinal fluid.

2003;21:401–7. 6. Ensenauer R, Muller CB, Schwab KO, Gibson KM, Brandis M, Lehnert W. 3-Methylglutaconyl-CoA hydratase deficiency: a new patient with speech retardation as the leading sign. J Inherit Metab Dis 2000;23:341–4. 7. Hou JW, Wang TR. 3-Methylglutaconic aciduria presenting as Reye syndrome in a Chinese boy. J Inherit Metab Dis 1995;18:645–6. 8. Jooste S, Erasmus E, Mienie LJ, de Wet WJ, Gibson KM. The detection of 3-methylglutarylcarnitine and a new dicarboxylic conjugate, 3-methylglutaconylcarnitine, in 3-methylglutaconic aciduria. Clin Chim Acta 1994;230:1–8. 9. Gibson KM, Lee CF, Wappner RS. 3-Methylglutaconyl-coenzyme-A hydratase deficiency: a new case. J Inherit Metab Dis 1992;15:363–6. 10. Arbelaez A, Castillo M, Stone J. MRI in 3-methylglutaconic aciduria type 1. Neuroradiology 1999;41:941–2. 11. Illsinger S, Lucke T, Zschocke J, Gibson KM, Das AM. 3-Methylglutaconic aciduria type I in a boy with fever-associated seizures. Pediatr Neurol 2004;30:213–5. 12. Narisawa K, Gibson KM, Sweetman L, Nyhan WL. 3-Methylglutaconyl-CoA hydratase, 3-methylcrotonyl-CoA carboxylase and 3-hydroxy-3-methylglutarylCoA lyase deficiencies: a coupled enzyme assay useful for their detection. Clin Chim Acta 1989;184:57–64. 13. Valianpour F, Wanders RJ, Overmars H, Vreken P, Van Gennip AH, Baas F, et al. Cardiolipin deficiency in X-linked cardioskeletal myopathy and neutropenia (Barth syndrome, MIM 302060): a study in cultured skin fibroblasts. J Pediatr 2002;141:729–33. 14. Gibson KM, Nyhan WL, Sweetman L, Narisawa K, Lehnert W, Divry P, et al. 3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normal. Eur J Pediatr 1988;148:76–82. 15. Wanders RJ, Denis S, Ruiter JP, Schutgens RB, van Roermund CW, Jacobs BS. Measurement of peroxisomal fatty acid -oxidation in cultured human skin fibroblasts. J Inherit Metab Dis 1995;18 Suppl 1:113–24. 16. Corkey BE. Analysis of acyl-coenzyme A esters in biological samples. Methods Enzymol 1988;166:55–70. 17. Roschinger W, Muntau AC, Duran M, Dorland L, IJlst L, Wanders RJ, et al. Carnitine-acylcarnitine translocase deficiency: metabolic consequences of an impaired mitochondrial carnitine cycle. Clin Chim Acta 2000;298:55–68. 18. Lazarow PB. Rat liver peroxisomes catalyze the oxidation of fatty acids. J Biol Chem 1978;253:1522–8. 19. Narisawa K, Gibson KM, Sweetman L, Nyhan WL, Duran M, Wadman SK. Deficiency of 3-methylglutaconyl-coenzyme A hydratase in two siblings with 3-methylglutaconic aciduria. J Clin Invest 1986;77:1148–52.