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Showing results (381-390 of 417) with videos related to

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Journal of Inherited Metabolic Disease|April 8, 2006
Expression profiling reveals multiple myelin alterations in murine succinate semialdehyde dehydrogenase deficiencyElizabeth A Donarum, Dietrich A Stephan, Kay Larkin, et al.
Molecular Genetics and Metabolism|October 4, 2012
Guanidinoacetate methyltransferase deficiency: first steps to newborn screening for a treatable neurometabolic diseaseS Mercimek-Mahmutoglu, G Sinclair, S J M van Dooren, et al.
Annals of Clinical Biochemistry|March 1, 1995
Three different methods for the determination of total homocysteine in plasmaM T te Poele-Pothoff, M van den Berg, D G Franken, et al.
Annals of Neurology|November 18, 1998
Clinical approach to inherited peroxisomal disorders: a series of 27 patientsM R Baumgartner, B T Poll-The, N M Verhoeven, et al.
Neurology|November 15, 2006
High frequency of creatine deficiency syndromes in patients with unexplained mental retardationL Lion-François, D Cheillan, G Pitelet, et al.
Archives of Internal Medicine|October 21, 2000
Hyperhomocysteinemia is associated with the presence of retinopathy in type 2 diabetes mellitus: the Hoorn studyE K Hoogeveen, P J Kostense, P E Eysink, et al.
Arzneimittel-Forschung|January 1, 1977
Interlaboratory variability of valproic acid determinationsD Schmidt, B Ferrandes, D Grandjean, et al.
Neurology|April 15, 2009
Combination of CSF N-acetylaspartate and neurofilaments in multiple sclerosisC E Teunissen, E Iacobaeus, M Khademi, et al.
Journal of Inherited Metabolic Disease|November 5, 1997
L-2-Hydroxyglutaric aciduria: normal L-2-hydroxyglutarate dehydrogenase activity in liver from two new patientsR J Wanders, L Vilarinho, H P Hartung, et al.
British Journal of Cancer|February 6, 2003
Changes in the ornithine cycle following ionising radiation cause a cytotoxic conditioning of the culture medium of H35 hepatoma cellsJ van Rijn, J van den Berg, T Teerlink, et al.
Pageof 42

Showing results (381-390 of 417) with videos related to

Sort By:
Pageof 42
Journal of Inherited Metabolic Disease|April 8, 2006
Expression profiling reveals multiple myelin alterations in murine succinate semialdehyde dehydrogenase deficiencyElizabeth A Donarum, Dietrich A Stephan, Kay Larkin, et al.
Molecular Genetics and Metabolism|October 4, 2012
Guanidinoacetate methyltransferase deficiency: first steps to newborn screening for a treatable neurometabolic diseaseS Mercimek-Mahmutoglu, G Sinclair, S J M van Dooren, et al.
Annals of Clinical Biochemistry|March 1, 1995
Three different methods for the determination of total homocysteine in plasmaM T te Poele-Pothoff, M van den Berg, D G Franken, et al.
Annals of Neurology|November 18, 1998
Clinical approach to inherited peroxisomal disorders: a series of 27 patientsM R Baumgartner, B T Poll-The, N M Verhoeven, et al.
Neurology|November 15, 2006
High frequency of creatine deficiency syndromes in patients with unexplained mental retardationL Lion-François, D Cheillan, G Pitelet, et al.
Archives of Internal Medicine|October 21, 2000
Hyperhomocysteinemia is associated with the presence of retinopathy in type 2 diabetes mellitus: the Hoorn studyE K Hoogeveen, P J Kostense, P E Eysink, et al.
Arzneimittel-Forschung|January 1, 1977
Interlaboratory variability of valproic acid determinationsD Schmidt, B Ferrandes, D Grandjean, et al.
Neurology|April 15, 2009
Combination of CSF N-acetylaspartate and neurofilaments in multiple sclerosisC E Teunissen, E Iacobaeus, M Khademi, et al.
Journal of Inherited Metabolic Disease|November 5, 1997
L-2-Hydroxyglutaric aciduria: normal L-2-hydroxyglutarate dehydrogenase activity in liver from two new patientsR J Wanders, L Vilarinho, H P Hartung, et al.
British Journal of Cancer|February 6, 2003
Changes in the ornithine cycle following ionising radiation cause a cytotoxic conditioning of the culture medium of H35 hepatoma cellsJ van Rijn, J van den Berg, T Teerlink, et al.
Pageof 42