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Neuropediatrics|May 10, 2023
Anterior Spinal Artery Syndrome Due to Fibrocartilaginous Embolism-Case Report and Treatment OptionsC Menke, I Wieland, E Bueltmann, et al.Amino Acids|December 22, 2004
Branched chain amino acids as a parameter for catabolism in treated phenylketonuriaS Illsinger, T Lücke, U Meyer, et al.Journal of Inherited Metabolic Disease|December 11, 2008
Developmental changes of oxalate excretion in enterally fed preterm infantsS Illsinger, T Lücke, B Vaske, et al.Archives of Disease in Childhood. Fetal and Neonatal Edition|November 13, 2008
Prenatal benzoate treatment in urea cycle defectsA M Das, S Illsinger, H Hartmann, et al.Journal of Inherited Metabolic Disease|November 7, 2009
Scheie syndrome: enzyme replacement therapy does not prevent progression of cervical myelopathy due to spinal cord compressionS Illsinger, T Lücke, H Hartmann, et al.JIMD Reports|November 14, 2013
Dietary habits and metabolic control in adolescents and young adults with phenylketonuria: self-imposed protein restriction may be harmfulA M Das, K Goedecke, U Meyer, et al.Neurology|September 22, 2010
3-Methylglutaconic aciduria type I redefined: a syndrome with late-onset leukoencephalopathyS B Wortmann, B H Kremer, A Graham, et al.Pageof 1