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C Jakobs

Showing results (321-330 of 417) with videos related to

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Circulation|April 4, 2000
Hyperhomocysteinemia increases risk of death, especially in type 2 diabetes : 5-year follow-up of the Hoorn StudyE K Hoogeveen, P J Kostense, C Jakobs, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
A new variant of Zellweger syndrome with normal peroxisomal functions in cultured fibroblastsR B Schutgens, R J Wanders, C Jakobs, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Stable isotope dilution analysis of N-acetylaspartic acid in CSF, blood, urine and amniotic fluid: accurate postnatal diagnosis and the potential for prenatal diagnosis of Canavan diseaseC Jakobs, H J ten Brink, S A Langelaar, et al.
Kidney International|July 2, 1998
Serum homocysteine level and protein intake are related to risk of microalbuminuria: the Hoorn StudyE K Hoogeveen, P J Kostense, A Jager, et al.
Neuropediatrics|August 30, 2000
Combined D-2- and L-2-hydroxyglutaric aciduria with neonatal onset encephalopathy: a third biochemical variant of 2-hydroxyglutaric aciduria?A C Muntau, W Röschinger, A Merkenschlager, et al.
The Netherlands Journal of Medicine|August 4, 1999
Variability of fasting and post-methionine plasma homocysteine levels in normo- and hyperhomocysteinaemic individualsM van den Berg, S C de Jong, W Devillé, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Organic acid profiles resembling a beta-oxidation defect in two patients with coeliac diseaseC G Costa, N M Verhoeven, C M Kneepkens, et al.
Journal of Inherited Metabolic Disease|August 2, 2003
X-linked creatine transporter defect: an overviewG S Salomons, S J M van Dooren, N M Verhoeven, et al.
Lancet (London, England)|July 1, 1989
Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenaseR J Wanders, M Duran, L Ijlst, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidationR J Wanders, L IJlst, A H van Gennip, et al.
Pageof 42

Showing results (321-330 of 417) with videos related to

Sort By:
Pageof 42
Circulation|April 4, 2000
Hyperhomocysteinemia increases risk of death, especially in type 2 diabetes : 5-year follow-up of the Hoorn StudyE K Hoogeveen, P J Kostense, C Jakobs, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
A new variant of Zellweger syndrome with normal peroxisomal functions in cultured fibroblastsR B Schutgens, R J Wanders, C Jakobs, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Stable isotope dilution analysis of N-acetylaspartic acid in CSF, blood, urine and amniotic fluid: accurate postnatal diagnosis and the potential for prenatal diagnosis of Canavan diseaseC Jakobs, H J ten Brink, S A Langelaar, et al.
Kidney International|July 2, 1998
Serum homocysteine level and protein intake are related to risk of microalbuminuria: the Hoorn StudyE K Hoogeveen, P J Kostense, A Jager, et al.
Neuropediatrics|August 30, 2000
Combined D-2- and L-2-hydroxyglutaric aciduria with neonatal onset encephalopathy: a third biochemical variant of 2-hydroxyglutaric aciduria?A C Muntau, W Röschinger, A Merkenschlager, et al.
The Netherlands Journal of Medicine|August 4, 1999
Variability of fasting and post-methionine plasma homocysteine levels in normo- and hyperhomocysteinaemic individualsM van den Berg, S C de Jong, W Devillé, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Organic acid profiles resembling a beta-oxidation defect in two patients with coeliac diseaseC G Costa, N M Verhoeven, C M Kneepkens, et al.
Journal of Inherited Metabolic Disease|August 2, 2003
X-linked creatine transporter defect: an overviewG S Salomons, S J M van Dooren, N M Verhoeven, et al.
Lancet (London, England)|July 1, 1989
Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenaseR J Wanders, M Duran, L Ijlst, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidationR J Wanders, L IJlst, A H van Gennip, et al.
Pageof 42