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Pediatric Research
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April 1, 1987
Clinical and biochemical variation and family studies in the multiple acyl-CoA dehydrogenation disorders
W J Rhead, J A Wolff, M Lipson, et al.
Prenatal Diagnosis
|
May 1, 1986
Activity of biotin-dependent and GABA metabolizing enzymes in chorionic villus samples: potential for 1st trimester prenatal diagnosis
F R Sweetman, K M Gibson, L Sweetman, et al.
The Journal of Clinical Investigation
|
May 1, 1987
Short-chain acyl-coenzyme A dehydrogenase deficiency. Clinical and biochemical studies in two patients
B A Amendt, C Greene, L Sweetman, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1982
Organic aciduria in neonatal multiple carboxylase deficiency
L Sweetman, W L Nyhan, N A Sakati, et al.
Radiography (London, England : 1995)
|
May 16, 2025
Automatic 3D camera positioning in cardiac computed tomography: A phantom study
Y H Hadi, A Legoff, N Moore, et al.
The New England Journal of Medicine
|
October 26, 1978
Transient hyperammonemia of the preterm infant
R A Ballard, B Vinocur, J W Reynolds, et al.
Biomedical & Environmental Mass Spectrometry
|
February 1, 1990
Stable isotope dilution analysis of 4-hydroxybutyric acid: an accurate method for quantification in physiological fluids and the prenatal diagnosis of 4-hydroxybutyric aciduria
K M Gibson, S Aramaki, L Sweetman, et al.
Journal of Neurogenetics
|
November 1, 1986
Multiple carboxylase deficiency due to deficiency of biotinidase
L P Thuy, B Zielinska, E Zammarchi, et al.
Journal of Neurogenetics
|
April 1, 1984
3-Hydroxy-3-methylglutaric aciduria
C L Greene, H M Cann, B H Robinson, et al.
Journal of Neurogenetics
|
April 1, 1985
Properties of succinic semialdehyde dehydrogenase in cultured human lymphoblasts
K M Gibson, L Sweetman, I Jansen, et al.
Page
of 18
Search research articles
Search
Showing results (141-150 of 175) with videos related to
Sort By:
Page
of 18
Pediatric Research
|
April 1, 1987
Clinical and biochemical variation and family studies in the multiple acyl-CoA dehydrogenation disorders
W J Rhead, J A Wolff, M Lipson, et al.
Prenatal Diagnosis
|
May 1, 1986
Activity of biotin-dependent and GABA metabolizing enzymes in chorionic villus samples: potential for 1st trimester prenatal diagnosis
F R Sweetman, K M Gibson, L Sweetman, et al.
The Journal of Clinical Investigation
|
May 1, 1987
Short-chain acyl-coenzyme A dehydrogenase deficiency. Clinical and biochemical studies in two patients
B A Amendt, C Greene, L Sweetman, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1982
Organic aciduria in neonatal multiple carboxylase deficiency
L Sweetman, W L Nyhan, N A Sakati, et al.
Radiography (London, England : 1995)
|
May 16, 2025
Automatic 3D camera positioning in cardiac computed tomography: A phantom study
Y H Hadi, A Legoff, N Moore, et al.
The New England Journal of Medicine
|
October 26, 1978
Transient hyperammonemia of the preterm infant
R A Ballard, B Vinocur, J W Reynolds, et al.
Biomedical & Environmental Mass Spectrometry
|
February 1, 1990
Stable isotope dilution analysis of 4-hydroxybutyric acid: an accurate method for quantification in physiological fluids and the prenatal diagnosis of 4-hydroxybutyric aciduria
K M Gibson, S Aramaki, L Sweetman, et al.
Journal of Neurogenetics
|
November 1, 1986
Multiple carboxylase deficiency due to deficiency of biotinidase
L P Thuy, B Zielinska, E Zammarchi, et al.
Journal of Neurogenetics
|
April 1, 1984
3-Hydroxy-3-methylglutaric aciduria
C L Greene, H M Cann, B H Robinson, et al.
Journal of Neurogenetics
|
April 1, 1985
Properties of succinic semialdehyde dehydrogenase in cultured human lymphoblasts
K M Gibson, L Sweetman, I Jansen, et al.
Page
of 18