Search research articles
Contact Us
Filters
Showing results (31-40 of 63) with videos related to
Page
of 7
Sort By:
Journal of Lipid Research
|
January 30, 1999
Analysis of pristanic acid beta-oxidation intermediates in plasma from healthy controls and patients affected with peroxisomal disorders by stable isotope dilution gas chromatography mass spectrometry
N M Verhoeven, D S Schor, E A Struys, et al.
European Journal of Pediatrics
|
March 29, 2001
Carnitine-acylcarnitine translocase deficiency: phenotype, residual enzyme activity and outcome
E Lopriore, R J Gemke, N M Verhoeven, et al.
American Journal of Human Genetics
|
April 28, 2001
X-linked creatine-transporter gene (SLC6A8) defect: a new creatine-deficiency syndrome
G S Salomons, S J van Dooren, N M Verhoeven, et al.
Journal of Inherited Metabolic Disease
|
July 1, 1997
Formation of 2,3-pristenic acid and 3-hydroxypristanic acid from pristanic acid in human liver
N M Verhoeven, D S Schor, G A Jansen, et al.
Annals of Neurology
|
March 23, 2001
Irreversible brain creatine deficiency with elevated serum and urine creatine: a creatine transporter defect?
K M Cecil, G S Salomons, W S Ball, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Clinical, biochemical, magnetic resonance imaging (MRI) and proton magnetic resonance spectroscopy (1H MRS) findings in a fourth case of combined D- and L-2 hydroxyglutaric aciduria
M-H Read, C Bonamy, D Laloum, et al.
Neurology
|
November 18, 1998
Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease
M R Baumgartner, N M Verhoeven, C Jakobs, et al.
Journal of Child Neurology
|
December 11, 1999
Increased cerebrospinal fluid glycine: a biochemical marker for a leukoencephalopathy with vanishing white matter
M S van der Knaap, R A Wevers, S Kure, et al.
Journal of Inherited Metabolic Disease
|
April 4, 2014
Comment on Zwickler et al.: Usefulness of biochemical parameters in decision-making on the start of emergency treatment in patients with propionic acidemia
M G M de Sain-van der Velden, M van der Ham, N M Verhoeven-Duif, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Organic acid profiles resembling a beta-oxidation defect in two patients with coeliac disease
C G Costa, N M Verhoeven, C M Kneepkens, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 63) with videos related to
Sort By:
Page
of 7
Journal of Lipid Research
|
January 30, 1999
Analysis of pristanic acid beta-oxidation intermediates in plasma from healthy controls and patients affected with peroxisomal disorders by stable isotope dilution gas chromatography mass spectrometry
N M Verhoeven, D S Schor, E A Struys, et al.
European Journal of Pediatrics
|
March 29, 2001
Carnitine-acylcarnitine translocase deficiency: phenotype, residual enzyme activity and outcome
E Lopriore, R J Gemke, N M Verhoeven, et al.
American Journal of Human Genetics
|
April 28, 2001
X-linked creatine-transporter gene (SLC6A8) defect: a new creatine-deficiency syndrome
G S Salomons, S J van Dooren, N M Verhoeven, et al.
Journal of Inherited Metabolic Disease
|
July 1, 1997
Formation of 2,3-pristenic acid and 3-hydroxypristanic acid from pristanic acid in human liver
N M Verhoeven, D S Schor, G A Jansen, et al.
Annals of Neurology
|
March 23, 2001
Irreversible brain creatine deficiency with elevated serum and urine creatine: a creatine transporter defect?
K M Cecil, G S Salomons, W S Ball, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Clinical, biochemical, magnetic resonance imaging (MRI) and proton magnetic resonance spectroscopy (1H MRS) findings in a fourth case of combined D- and L-2 hydroxyglutaric aciduria
M-H Read, C Bonamy, D Laloum, et al.
Neurology
|
November 18, 1998
Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease
M R Baumgartner, N M Verhoeven, C Jakobs, et al.
Journal of Child Neurology
|
December 11, 1999
Increased cerebrospinal fluid glycine: a biochemical marker for a leukoencephalopathy with vanishing white matter
M S van der Knaap, R A Wevers, S Kure, et al.
Journal of Inherited Metabolic Disease
|
April 4, 2014
Comment on Zwickler et al.: Usefulness of biochemical parameters in decision-making on the start of emergency treatment in patients with propionic acidemia
M G M de Sain-van der Velden, M van der Ham, N M Verhoeven-Duif, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Organic acid profiles resembling a beta-oxidation defect in two patients with coeliac disease
C G Costa, N M Verhoeven, C M Kneepkens, et al.
Page
of 7