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Annals of Neurology
|
January 13, 2000
Atypical refsum disease with pipecolic acidemia and abnormal catalase distribution
M R Baumgartner, G A Jansen, N M Verhoeven, et al.
Analytica Chimica Acta
|
December 20, 2011
Quantification of vitamin B6 vitamers in human cerebrospinal fluid by ultra performance liquid chromatography-tandem mass spectrometry
M van der Ham, M Albersen, T J de Koning, et al.
Molecular Genetics and Metabolism
|
January 31, 2006
D-2-hydroxyglutaric aciduria in three patients with proven SSADH deficiency: genetic coincidence or a related biochemical epiphenomenon?
E A Struys, N M Verhoeven, G S Salomons, et al.
Journal of Inherited Metabolic Disease
|
December 16, 2006
Guanidinoacetate methyltransferase deficiency masquerading as a mitochondrial encephalopathy
A A M Morris, R E Appleton, B Power, et al.
Annals of Neurology
|
November 18, 1998
Clinical approach to inherited peroxisomal disorders: a series of 27 patients
M R Baumgartner, B T Poll-The, N M Verhoeven, et al.
Tijdschrift Voor Psychiatrie
|
May 24, 2016
[Metabolic diseases in psychiatry]
M G M De Sain-Van der Velden, J J Jans, M Figee, et al.
Journal of Inherited Metabolic Disease
|
April 22, 2016
Rapid quantification of underivatized amino acids in plasma by hydrophilic interaction liquid chromatography (HILIC) coupled with tandem mass-spectrometry
Hubertus C M T Prinsen, B G M Schiebergen-Bronkhorst, M W Roeleveld, et al.
Neurology
|
July 2, 2008
Reduced brain choline in homocystinuria due to remethylation defects
F-G Debray, Y Boulanger, A Khiat, et al.
Scientific Reports
|
October 15, 2017
Saline is as effective as nitrogen scavengers for treatment of hyperammonemia
G van Straten, M G M de Sain-van der Velden, I M van Geijlswijk, et al.
Human Mutation
|
September 1, 2005
Novel L2HGDH mutations in 21 patients with L-2-hydroxyglutaric aciduria of Portuguese origin
L Vilarinho, M L Cardoso, P Gaspar, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 63) with videos related to
Sort By:
Page
of 7
Annals of Neurology
|
January 13, 2000
Atypical refsum disease with pipecolic acidemia and abnormal catalase distribution
M R Baumgartner, G A Jansen, N M Verhoeven, et al.
Analytica Chimica Acta
|
December 20, 2011
Quantification of vitamin B6 vitamers in human cerebrospinal fluid by ultra performance liquid chromatography-tandem mass spectrometry
M van der Ham, M Albersen, T J de Koning, et al.
Molecular Genetics and Metabolism
|
January 31, 2006
D-2-hydroxyglutaric aciduria in three patients with proven SSADH deficiency: genetic coincidence or a related biochemical epiphenomenon?
E A Struys, N M Verhoeven, G S Salomons, et al.
Journal of Inherited Metabolic Disease
|
December 16, 2006
Guanidinoacetate methyltransferase deficiency masquerading as a mitochondrial encephalopathy
A A M Morris, R E Appleton, B Power, et al.
Annals of Neurology
|
November 18, 1998
Clinical approach to inherited peroxisomal disorders: a series of 27 patients
M R Baumgartner, B T Poll-The, N M Verhoeven, et al.
Tijdschrift Voor Psychiatrie
|
May 24, 2016
[Metabolic diseases in psychiatry]
M G M De Sain-Van der Velden, J J Jans, M Figee, et al.
Journal of Inherited Metabolic Disease
|
April 22, 2016
Rapid quantification of underivatized amino acids in plasma by hydrophilic interaction liquid chromatography (HILIC) coupled with tandem mass-spectrometry
Hubertus C M T Prinsen, B G M Schiebergen-Bronkhorst, M W Roeleveld, et al.
Neurology
|
July 2, 2008
Reduced brain choline in homocystinuria due to remethylation defects
F-G Debray, Y Boulanger, A Khiat, et al.
Scientific Reports
|
October 15, 2017
Saline is as effective as nitrogen scavengers for treatment of hyperammonemia
G van Straten, M G M de Sain-van der Velden, I M van Geijlswijk, et al.
Human Mutation
|
September 1, 2005
Novel L2HGDH mutations in 21 patients with L-2-hydroxyglutaric aciduria of Portuguese origin
L Vilarinho, M L Cardoso, P Gaspar, et al.
Page
of 7