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Pediatric Research
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November 1, 1992
In vivo study of phytanic acid alpha-oxidation in classic Refsum's disease and chondrodysplasia punctata
H J ten Brink, D S Schor, R M Kok, et al.
European Journal of Pediatrics
|
May 20, 1999
N-acetylaspartylglutamate in Canavan disease: an adverse effector?
A P Burlina, V Ferrari, P Divry, et al.
Lancet (London, England)
|
September 19, 1987
Lactitol, lactulose, and blood ammonia
A C Douwes, G J van der Burg, A A Bouman, et al.
Journal of Inherited Metabolic Disease
|
May 10, 2002
D-2-Hydroxyglutaric aciduria in a patient with a severe clinical phenotype and unusual MRI findings
M Wajne, C R Vargas, C Funayama, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
March 9, 2000
Quantitative analysis of urinary acylglycines for the diagnosis of beta-oxidation defects using GC-NCI-MS
C G Costa, W S Guérand, E A Struys, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
May 14, 1999
Determinants of fasting and post-methionine homocysteine levels in families predisposed to hyperhomocysteinemia and premature vascular disease
S C de Jong, C D Stehouwer, M van den Berg, et al.
The Netherlands Journal of Medicine
|
March 23, 2000
Normohomocysteinaemia and vitamin-treated hyperhomocysteinaemia are associated with similar risks of cardiovascular events in patients with premature atherothrombotic cerebrovascular disease. A prospective cohort study
E G Vermeulen, J A Rauwerda, P Erix, et al.
American Journal of Obstetrics and Gynecology
|
October 1, 1995
Underlying disorders associated with severe early-onset preeclampsia
G A Dekker, J I de Vries, P M Doelitzsch, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
January 28, 1998
Hyperhomocysteinemia is associated with an increased risk of cardiovascular disease, especially in non-insulin-dependent diabetes mellitus: a population-based study
E K Hoogeveen, P J Kostense, P J Beks, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1998
Unusual enzyme findings in five patients with metabolic profiles suggestive of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria)
K M Gibson, L Sweetman, V Kozich, et al.
Page
of 42
Search research articles
Search
Showing results (331-340 of 417) with videos related to
Sort By:
Page
of 42
Pediatric Research
|
November 1, 1992
In vivo study of phytanic acid alpha-oxidation in classic Refsum's disease and chondrodysplasia punctata
H J ten Brink, D S Schor, R M Kok, et al.
European Journal of Pediatrics
|
May 20, 1999
N-acetylaspartylglutamate in Canavan disease: an adverse effector?
A P Burlina, V Ferrari, P Divry, et al.
Lancet (London, England)
|
September 19, 1987
Lactitol, lactulose, and blood ammonia
A C Douwes, G J van der Burg, A A Bouman, et al.
Journal of Inherited Metabolic Disease
|
May 10, 2002
D-2-Hydroxyglutaric aciduria in a patient with a severe clinical phenotype and unusual MRI findings
M Wajne, C R Vargas, C Funayama, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
March 9, 2000
Quantitative analysis of urinary acylglycines for the diagnosis of beta-oxidation defects using GC-NCI-MS
C G Costa, W S Guérand, E A Struys, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
May 14, 1999
Determinants of fasting and post-methionine homocysteine levels in families predisposed to hyperhomocysteinemia and premature vascular disease
S C de Jong, C D Stehouwer, M van den Berg, et al.
The Netherlands Journal of Medicine
|
March 23, 2000
Normohomocysteinaemia and vitamin-treated hyperhomocysteinaemia are associated with similar risks of cardiovascular events in patients with premature atherothrombotic cerebrovascular disease. A prospective cohort study
E G Vermeulen, J A Rauwerda, P Erix, et al.
American Journal of Obstetrics and Gynecology
|
October 1, 1995
Underlying disorders associated with severe early-onset preeclampsia
G A Dekker, J I de Vries, P M Doelitzsch, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
January 28, 1998
Hyperhomocysteinemia is associated with an increased risk of cardiovascular disease, especially in non-insulin-dependent diabetes mellitus: a population-based study
E K Hoogeveen, P J Kostense, P J Beks, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1998
Unusual enzyme findings in five patients with metabolic profiles suggestive of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria)
K M Gibson, L Sweetman, V Kozich, et al.
Page
of 42