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Browsing by Author Wendel, U.A.H.

Full Text	Issue Date	Title	Author(s)
	1997	Clinical heterogenity in respiratory chain complex III deficiency in childhood	Mourmans, J.; Wendel, U.A.H.; Bentlage, H.A.C.M., et al
	2007	Cystic renal dysplasia as a leading sign of inherited metabolic disease.	Distelmaier, F.; Vogel, M.; Spiekerkotter, U., et al
	1997	Defects in the mitochondrial energy metabolism outside the respiratory chain and the pyruvate dehydrogenase complex	Trijbels, J.M.F.; Ruitenbeek, W.; Huizing, M., et al
	1995	Enzymatic method for determination of branched-chain amino acid aminotransferase activity	Schadewaldt, P.; Hummel, W.; Wendel, U.A.H., et al
	1995	Enzymatic-chemical preparation of quinoxaline derivatives from L-amino acids for gas chromatographic-mass spectrometric analyses	Schadewaldt, P.; Hammen, H.W.; Wendel, U.A.H., et al
	1995	Evaluation of prenatal treatment in newborns with cobalamin-responsive methylmalonic acidaemia	Zaß, R.; Leupold, D.; Fernandez, M.A., et al
	1996	Genetic counselling and prenatal diagnosis in disorders of the mitochondrial energy metabolism	Ruitenbeek, W.; Wendel, U.A.H.; Hamel, B.C.J., et al
	1995	Glutaric aciduria mediated by gut bacteria	Wendel, U.A.H.; Bakkeren, J.A.J.; Jong, J.G.N. de, et al
	1995	Glutaric aciduria mediated by gut bacteria	Wendel, U.A.H.; Bakkeren, J.A.J.; Jong, J.G.N. de, et al
	1995	Human branched-chain L-amino acid aminotransferase: Activity and subcellular localization in cultured skin fibroblasts	Schadewaldt, P.; Wendel, U.A.H.; Hammen, H.W.
	1996	Importance of mitochondrial transmembrane processes in human mitochondriopathies.	Huizing, M.; Pinto, V. de; Ruitenbeek, W., et al
	1995	Isolated (biotin-resistant) 3-methylcrotonyl-CoA carboxylase deficiency: four sibs devoid of pathology	Mourmans, J.; Bakkeren, J.A.J.; Jong, J.G.N. de, et al
	1995	Isolated (biotin-resistant) 3-methylcrotonyl-CoA carboxylase deficiency: four sibs devoid of pathology.	Mourmans, J.; Bakkeren, J.A.J.; Jong, J.G.N. de, et al
	1995	Liver transplantation in two cases of propionic acidaemia	Schlenzig, J.S.; Poggi-Travert, F.; Laurent, J., et al
	1995	Neonatal De Toni-Debré-Fanconi syndrome due to a defect in complex III of the respiratory chain	Wendel, U.A.H.; Ruitenbeek, W.; Bentlage, H.A.C.M., et al
	1997	Neonatal lethal mitochondrial trifunctional protein (MTP) deficiency mimicking a respiratory chain defect	Grunewald, S.; Bakkeren, J.A.J.; Wanders, R.J.A., et al
	1995	On the differences between urinary metabolite excretion and odd-numbered fatty acid production in propionic and methylmalonic acidaemias	Wendel, U.A.H.; Eißler, A.; Sperl, W., et al
	1997	Pitfalls in measuring plasma cholesterol in the Smith-Lemli-Opitz syndrome	Jira, P.E.; Jong, J.G.N. de; Janssem-Zijlstra, F.S.M., et al
	1995	Proton magnetic resonance spectroscopy reflects metabolic decompensation in maple syrup urine disease	Heindel, W.; Kugel, H.; Wendel, U.A.H., et al
	1995	Standardized method for high-resolution 1H-NMR of cerebrospinal fluid	Wevers, R.A.; Engelke, U.F.H.; Wendel, U.A.H., et al