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Journal of Inherited Metabolic Disease|March 21, 2013
Current concepts in organic acidurias: understanding intra- and extracerebral disease manifestationStefan Kölker, Peter Burgard, Sven W Sauer, et al.
Annals of Neurology|January 6, 2004
Pathomechanisms of neurodegeneration in glutaryl-CoA dehydrogenase deficiencyStefan Kölker, David M Koeller, Jürgen G Okun, et al.
Parkinsonism & Related Disorders|January 24, 2007
Nitrous oxide promotes hyperhomocysteinemia in levodopa treated ratsNils Henninger, Qi Wang, Jürgen G Okun, et al.
Journal of Inherited Metabolic Disease|July 30, 2010
Phenylalanine loading in pediatric patients with dopa-responsive dystonia: revised test protocol and pediatric cutoff valuesThomas Opladen, Jürgen G Okun, Peter Burgard, et al.
European Journal of Clinical Investigation|June 26, 2015
Ursodeoxycholyl Lysophosphatidylethanolamide modifies aberrant lipid profiles in NAFLDAnita Pathil, Gerhard Liebisch, Jürgen G Okun, et al.
Journal of Inherited Metabolic Disease|November 4, 2017
Impairment of astrocytic glutaminolysis in glutaric aciduria type IShoko Komatsuzaki, Raga Deepthi Ediga, Jürgen G Okun, et al.
Molecular Genetics and Metabolism|July 25, 2018
Relationship between genotype, phenylalanine hydroxylase expression and in vitro activity and metabolic phenotype in phenylketonuriaNastassja Himmelreich, Nan Shen, Jürgen G Okun, et al.
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