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Journal of Inherited Metabolic Disease|March 18, 2003
Emergency management of inherited metabolic diseasesV Prietsch, M Lindner, J Zschocke, et al.Early Human Development|May 13, 1999
Increased energy expenditure and fecal fat excretion do not impair weight gain in small-for-gestational-age preterm infantsT Böhler, T Krämer, A R Janecke, et al.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|July 1, 1990
[Pre- and postnatal diagnosis of organoacidopathies]G F Hoffmann, C Jakobs, D Rating, et al.The Journal of Pediatrics|March 1, 1996
Severe hyperchloriduria-hyperkaliuria: a new congenital renal tubular abnormality?J Meyburg, E Mayatepek, G F Hoffmann, et al.Journal of Inherited Metabolic Disease|June 10, 2006
Neonatal screening for glutaric aciduria type I: strategies to proceedM Lindner, S Ho, J Fang-Hoffmann, et al.Lancet (London, England)|September 15, 1999
Mild trimethylaminuria caused by common variants in FMO3 geneJ Zschocke, D Kohlmueller, E Quak, et al.The European Journal of Neuroscience|June 26, 2001
Potentiation of 3-hydroxyglutarate neurotoxicity following induction of astrocytic iNOS in neonatal rat hippocampal culturesS Kölker, B Ahlemeyer, R Hühne, et al.European Journal of Dermatology : EJD|May 19, 2001
Acrodermatitis acidemica secondary to malnutrition in glutaric aciduria type IS Niiyama, S Koelker, I Degen, et al.Neuropediatrics|May 1, 1999
A severely affected infant with absence of cysteinyl leukotrienes in cerebrospinal fluid: further evidence that leukotriene C4-synthesis deficiency is a new neurometabolic disorderE Mayatepek, M Lindner, R Zelezny, et al.Journal of Inherited Metabolic Disease|June 20, 2008
Newborn screening for methylmalonic acidurias--optimization by statistical parameter combinationM Lindner, S Ho, S Kölker, et al.Pageof 18