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European Journal of Pediatrics|January 1, 1994
Screening for defects of branched-chain amino acid metabolismK M Gibson, C F Lee, G F HoffmannPediatric Research|April 12, 2000
Maturation-dependent neurotoxicity of 3-hydroxyglutaric and glutaric acids in vitro: a new pathophysiologic approach to glutaryl-CoA dehydrogenase deficiencyS Kölker, B Ahlemeyer, J Krieglstein, et al.Clinical Chemistry|July 27, 2001
Spectrophotometric microassay for delta-aminolevulinate dehydratase in dried-blood spots as confirmation for hereditary tyrosinemia type IA Schulze, D Frommhold, G F Hoffmann, et al.Pediatric Neurology|September 12, 2001
Cranial MRI changes may precede symptoms in Hallervorden-Spatz syndromeS J Hayflick, J M Penzien, W Michl, et al.Neuropediatrics|June 25, 1998
Cerebrospinal fluid investigations for neurometabolic disordersG F Hoffmann, R A Surtees, R A WeversJournal of Medical Genetics|March 4, 2000
Mutation analysis in glutaric aciduria type IJ Zschocke, E Quak, P Guldberg, et al.Schweizerische Medizinische Wochenschrift|November 21, 1992
[Glomerulonephritis with transient C3 hypoclompimentemia and endotheliomesangial glomerulonephritis in childhood. A long-term experience]M J Rimediotti, M G Bianchetti, J M Penzien, et al.Diabetologia|August 10, 1999
Impaired deformability of erythrocytes and neutrophils in children with newly diagnosed insulin-dependent diabetes mellitusO Linderkamp, P Ruef, E P Zilow, et al.The Journal of Pediatrics|February 15, 2001
Acute encephalopathy despite early therapy in a patient with homozygosity for E365K in the glutaryl-coenzyme A dehydrogenase geneS Kölker, V T Ramaekers, J Zschocke, et al.Journal of Inherited Metabolic Disease|September 14, 2002
Neurotransmitter metabolites in CSF: an external quality control schemeC Bräutigam, C Weykamp, G F Hoffmann, et al.Pageof 18