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Human Genomics
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January 24, 2009
Comparative genomics of aldehyde dehydrogenase 5a1 (succinate semialdehyde dehydrogenase) and accumulation of gamma-hydroxybutyrate associated with its deficiency
Patrizia Malaspina, Matthew J Picklo, C Jakobs, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Bile acids in amniotic fluid: promising metabolites for the prenatal diagnosis of peroxisomal disorders
F Stellaard, W J Kleijer, R J Wanders, et al.
Prenatal Diagnosis
|
March 1, 1996
A case of tyrosinaemia type I with normal level of succinylacetone in the amniotic fluid
A Grenier, S Cederbaum, C Laberge, et al.
Journal of Inherited Metabolic Disease
|
April 8, 2006
Homocysteine metabolism, hyperhomocysteinaemia and vascular disease: an overview
R Castro, I Rivera, H J Blom, et al.
European Journal of Clinical Investigation
|
March 27, 1999
Neurone-specific enolase and N-acetyl-aspartate as potential peripheral markers of ischaemic stroke
H Stevens, C Jakobs, A E de Jager, et al.
Kidney International
|
January 20, 1999
Plasma homocysteine concentration predicts mortality in non-insulin-dependent diabetic patients with and without albuminuria
C D Stehouwer, M A Gall, P Hougaard, et al.
European Journal of Pediatrics
|
July 1, 1985
Prenatal diagnosis of tyrosinaemia type I by use of stable isotope dilution mass spectrometry
C Jakobs, E A Kvittingen, R Berger, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Renal failure in adult patients with hereditary tyrosinaemia type I
E A Kvittingen, T Talseth, S Halvorsen, et al.
Acta Chirurgiae Orthopaedicae Et Traumatologiae Cechoslovaca
|
April 24, 2014
Lower limb salvage: indication and decision making for replantation, revascularisation and amputation
S Märdian, K D Schaser, F Wichlas, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Major hyperpipecolataemia in a normal adult
C Vallat, S Denis, H Bellet, et al.
Page
of 42
Search research articles
Search
Showing results (111-120 of 417) with videos related to
Sort By:
Page
of 42
Human Genomics
|
January 24, 2009
Comparative genomics of aldehyde dehydrogenase 5a1 (succinate semialdehyde dehydrogenase) and accumulation of gamma-hydroxybutyrate associated with its deficiency
Patrizia Malaspina, Matthew J Picklo, C Jakobs, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Bile acids in amniotic fluid: promising metabolites for the prenatal diagnosis of peroxisomal disorders
F Stellaard, W J Kleijer, R J Wanders, et al.
Prenatal Diagnosis
|
March 1, 1996
A case of tyrosinaemia type I with normal level of succinylacetone in the amniotic fluid
A Grenier, S Cederbaum, C Laberge, et al.
Journal of Inherited Metabolic Disease
|
April 8, 2006
Homocysteine metabolism, hyperhomocysteinaemia and vascular disease: an overview
R Castro, I Rivera, H J Blom, et al.
European Journal of Clinical Investigation
|
March 27, 1999
Neurone-specific enolase and N-acetyl-aspartate as potential peripheral markers of ischaemic stroke
H Stevens, C Jakobs, A E de Jager, et al.
Kidney International
|
January 20, 1999
Plasma homocysteine concentration predicts mortality in non-insulin-dependent diabetic patients with and without albuminuria
C D Stehouwer, M A Gall, P Hougaard, et al.
European Journal of Pediatrics
|
July 1, 1985
Prenatal diagnosis of tyrosinaemia type I by use of stable isotope dilution mass spectrometry
C Jakobs, E A Kvittingen, R Berger, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Renal failure in adult patients with hereditary tyrosinaemia type I
E A Kvittingen, T Talseth, S Halvorsen, et al.
Acta Chirurgiae Orthopaedicae Et Traumatologiae Cechoslovaca
|
April 24, 2014
Lower limb salvage: indication and decision making for replantation, revascularisation and amputation
S Märdian, K D Schaser, F Wichlas, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Major hyperpipecolataemia in a normal adult
C Vallat, S Denis, H Bellet, et al.
Page
of 42