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Multiple Sclerosis (Houndmills, Basingstoke, England)|July 27, 2013
Neuromyelitis optica and pregnancy during therapeutic B cell depletion: infant exposure to anti-AQP4 antibody and prevention of rebound relapses with low-dose rituximab postpartumM Ringelstein, J Harmel, F Distelmaier, et al.Neuropediatrics|August 18, 2001
Hydrocephalus internus in two patients with 5,10-methylenetetrahydrofolate reductase deficiencyM Baethmann, U Wendel, G F Hoffmann, et al.Journal of Inherited Metabolic Disease|October 27, 2004
Looking forward--an evidence-based approach to glutaryl-CoA dehydrogenase deficiencyS Kölker, P Burgard, J G Okun, et al.Journal of Inherited Metabolic Disease|June 10, 2006
Carnitine supplementation induces long-chain acylcarnitine production--studies in the VLCAD-deficient mouseM Liebig, M Gyenes, G Brauers, et al.Pediatric Research|December 1, 1992
Atypical (mild) forms of dihydropteridine reductase deficiency: neurochemical evaluation and mutation detectionN Blau, C W Heizmann, W Sperl, et al.Journal of Inherited Metabolic Disease|September 12, 2007
Neurodegeneration and chronic renal failure in methylmalonic aciduria--a pathophysiological approachM A Morath, J G Okun, I B Müller, et al.Journal of Inherited Metabolic Disease|November 6, 2008
Qualitative urinary organic acid analysis: methodological approaches and performanceV Peters, S F Garbade, C D Langhans, et al.Neuropediatrics|August 18, 2001
Atypical and variable clinical presentation of glutaric aciduria type ID I Zafeiriou, J Zschocke, P Augoustidou-Savvopoulou, et al.Pediatric Research|August 1, 1993
Decreased plasma ubiquinone-10 concentration in patients with mevalonate kinase deficiencyC Hübner, G F Hoffmann, C Charpentier, et al.The Journal of Pediatrics|December 5, 1997
Creatine deficiency syndrome caused by guanidinoacetate methyltransferase deficiency: diagnostic tools for a new inborn error of metabolismA Schulze, T Hess, R Wevers, et al.Pageof 28