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The New England Journal of Medicine
|
December 23, 1976
Jamaican vomiting sickness and Reye's syndrome
D A Trauner, W L Nyhan, L Sweetman
Archives of Neurology
|
February 1, 1977
EEG correlations with biochemical abnormalities in Reye syndrome
D A Trauner, J J Stockard, L Sweetman
The New England Journal of Medicine
|
April 2, 1981
Biotin-responsive carboxylase deficiency associated with subnormal plasma and urinary biotin
J Thoene, H Baker, M Yoshino, et al.
The New England Journal of Medicine
|
August 17, 1978
A syndrome of methylmalonic aciduria, homocystinuria, megaloblastic anemia and neurologic abnormalities in a vitamin B12-deficient breast-fed infant of a strict vegetarian
M C Higginbottom, L Sweetman, W L Nyhan
The Journal of Clinical Investigation
|
December 1, 1981
Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency
B J Burri, L Sweetman, W L Nyhan
The Journal of Clinical Investigation
|
December 1, 1979
Inhibition by propionyl-coenzyme A of N-acetylglutamate synthetase in rat liver mitochondria. A possible explanation for hyperammonemia in propionic and methylmalonic acidemia
F X Coude, L Sweetman, W L Nyhan
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 31, 1990
Enzymatic diagnosis of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency with high-performance liquid chromatography
M Kikuchi, K Narisawa, K Tada, et al.
Clinical Pediatrics
|
May 4, 2007
Gelastic seizures misdiagnosed as gastroesophageal reflux disease
Laura L Sweetman, Yu-Tze Ng, John F Kerrigan
Journal of Inherited Metabolic Disease
|
January 1, 1984
Stable isotope dilution analysis of 3-hydroxyisovaleric acid in amniotic fluid: contribution to the prenatal diagnosis of inherited disorders of leucine catabolism
C Jakobs, L Sweetman, W L Nyhan, et al.
Journal of Neurogenetics
|
December 1, 1985
Metabolism of leucine in fibroblasts from patients with deficiencies in each of the major catabolic enzymes: branched-chain ketoacid dehydrogenase, isovaleryl-CoA dehydrogenase, 3-methylcrotonyl-CoA carboxylase, 3-methylglutaconyl-CoA hydratase, and 3-hydroxy-3-methylglutaryl-CoA lyase
I Yoshida, O Søvik, L Sweetman, et al.
Page
of 18
Search research articles
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Showing results (41-50 of 175) with videos related to
Sort By:
Page
of 18
The New England Journal of Medicine
|
December 23, 1976
Jamaican vomiting sickness and Reye's syndrome
D A Trauner, W L Nyhan, L Sweetman
Archives of Neurology
|
February 1, 1977
EEG correlations with biochemical abnormalities in Reye syndrome
D A Trauner, J J Stockard, L Sweetman
The New England Journal of Medicine
|
April 2, 1981
Biotin-responsive carboxylase deficiency associated with subnormal plasma and urinary biotin
J Thoene, H Baker, M Yoshino, et al.
The New England Journal of Medicine
|
August 17, 1978
A syndrome of methylmalonic aciduria, homocystinuria, megaloblastic anemia and neurologic abnormalities in a vitamin B12-deficient breast-fed infant of a strict vegetarian
M C Higginbottom, L Sweetman, W L Nyhan
The Journal of Clinical Investigation
|
December 1, 1981
Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency
B J Burri, L Sweetman, W L Nyhan
The Journal of Clinical Investigation
|
December 1, 1979
Inhibition by propionyl-coenzyme A of N-acetylglutamate synthetase in rat liver mitochondria. A possible explanation for hyperammonemia in propionic and methylmalonic acidemia
F X Coude, L Sweetman, W L Nyhan
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 31, 1990
Enzymatic diagnosis of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency with high-performance liquid chromatography
M Kikuchi, K Narisawa, K Tada, et al.
Clinical Pediatrics
|
May 4, 2007
Gelastic seizures misdiagnosed as gastroesophageal reflux disease
Laura L Sweetman, Yu-Tze Ng, John F Kerrigan
Journal of Inherited Metabolic Disease
|
January 1, 1984
Stable isotope dilution analysis of 3-hydroxyisovaleric acid in amniotic fluid: contribution to the prenatal diagnosis of inherited disorders of leucine catabolism
C Jakobs, L Sweetman, W L Nyhan, et al.
Journal of Neurogenetics
|
December 1, 1985
Metabolism of leucine in fibroblasts from patients with deficiencies in each of the major catabolic enzymes: branched-chain ketoacid dehydrogenase, isovaleryl-CoA dehydrogenase, 3-methylcrotonyl-CoA carboxylase, 3-methylglutaconyl-CoA hydratase, and 3-hydroxy-3-methylglutaryl-CoA lyase
I Yoshida, O Søvik, L Sweetman, et al.
Page
of 18