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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.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1992
[Kawasaki syndrome. Association with exposure to carpet shampoo and successful therapy with immunoglobulins in the second week of the illness]E Blum-Hoffmann, G F Hoffmann, A Wessel, et al.The Journal of Pediatrics|May 29, 1998
The clinical manifestation of the kwashiorkor syndrome is related to increased lipid peroxidationH Lenhartz, R Ndasi, A Anninos, et al.Human Mutation|December 29, 1999
Two novel missense mutations of the OCTN2 gene (W283R and V446F) in a patient with primary systemic carnitine deficiencyE Mayatepek, J Nezu, I Tamai, et al.Neuropediatrics|April 25, 2000
2-ketoglutarate dehydrogenase deficiency with intermittent 2-ketoglutaric aciduriaR J Dunckelmann, F Ebinger, A Schulze, et al.Ultrasound International Open|October 1, 2016
Evaluation of Acoustic Radiation Force Impulse Imaging (ARFI) for the Determination of Liver Stiffness Using Transient Elastography as a Reference in ChildrenA Sagir, D Ney, J Oh, et al.Journal of Chromatography. B, Biomedical Sciences and Applications|November 21, 1998
Specific and rapid quantification of 8-iso-prostaglandin F2alpha in urine of healthy humans and patients with Zellweger syndrome by gas chromatography-tandem mass spectrometryD Tsikas, E Schwedhelm, J Fauler, et al.Allergy|September 12, 2001
Urinary leukotriene E(4), eosinophil protein X, and nasal eosinophil cationic protein are not associated with respiratory symptoms in 1-year-old childrenC Wojnarowski, G Halmerbauer, E Mayatepek, et al.The European Respiratory Journal|June 15, 2006
Endothelial, inducible and neuronal nitric oxide synthase in congenital pulmonary lymphangiectasisT Hoehn, M William, A R McPhaden, et al.Pageof 28