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Neuroradiology|March 20, 2016
MRI and (1)H-MRS in adenosine kinase deficiencyC Staufner, H J Blom, C Dionisi-Vici, et al.Pediatric Research|September 1, 1993
Stable-isotope dilution analysis of D- and L-2-hydroxyglutaric acid: application to the detection and prenatal diagnosis of D- and L-2-hydroxyglutaric acidemiasK M Gibson, H J ten Brink, D S Schor, et al.Journal of Inherited Metabolic Disease|July 13, 2004
Sedation with 4-hydroxybutyric acid: a potential pitfall in the diagnosis of SSADH deficiencyN I Wolf, D Haas, G F Hoffmann, et al.Journal of Inherited Metabolic Disease|October 27, 2004
Maintenance treatment of glutaryl-CoA dehydrogenase deficiencyC Mühlhausen, G F Hoffmann, K A Strauss, et al.American Journal of Medical Genetics|August 26, 1998
Hematological abnormalities and cholestatic liver disease in two patients with mevalonate kinase deficiencyD D Hinson, Z R Rogers, G F Hoffmann, et al.Brain : a Journal of Neurology|June 16, 2001
Clinical, biochemical and molecular genetic characteristics of 19 patients with the Sjögren-Larsson syndromeM A Willemsen, L IJlst, P M Steijlen, et al.Journal of Inherited Metabolic Disease|June 9, 2009
Coenzyme Q(10) is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduriaD Haas, P Niklowitz, F Hörster, et al.Journal of Inherited Metabolic Disease|August 18, 2009
Mental retardation and inborn errors of metabolismA García-Cazorla, N I Wolf, M Serrano, et al.Journal of Inherited Metabolic Disease|May 15, 2007
Effects of cholesterol and simvastatin treatment in patients with Smith-Lemli-Opitz syndrome (SLOS)D Haas, S F Garbade, C Vohwinkel, et al.Child Psychiatry and Human Development|May 20, 2014
Health-related quality of life in adolescents with inflammatory bowel disease depends on disease activity and psychiatric comorbidityG Engelmann, D Erhard, M Petersen, et al.Pageof 28