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Journal of Inherited Metabolic Disease
|
January 1, 1992
3-Methylglutaconyl-coenzyme-A hydratase deficiency: a new case
K M Gibson, C F Lee, R S Wappner
European Journal of Pediatrics
|
January 1, 1994
Screening for defects of branched-chain amino acid metabolism
K M Gibson, C F Lee, G F Hoffmann
Journal of Virological Methods
|
May 1, 1991
A simple and rapid method for detecting human immunodeficiency virus by PCR
K M Gibson, K A McLean, J P Clewley
Journal of Inherited Metabolic Disease
|
January 1, 1996
beta-Ketothiolase (2-methylacetoacetyl-coenzyme A thiolase) deficiency: identification of two patients in Israel
K M Gibson, O N Elpeleg, M J Bennett
Comparative Biochemistry and Physiology. Part A, Physiology
|
October 1, 1995
gamma-Aminobutyric acid (GABA) metabolism in mammalian neural and nonneural tissues
N J Tillakaratne, L Medina-Kauwe, K M Gibson
Journal of Inherited Metabolic Disease
|
January 1, 1996
Seizures in a boy with succinic semialdehyde dehydrogenase deficiency treated with vigabatrin (gamma-vinyl-GABA)
D Matern, W Lehnert, K M Gibson, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 31, 1992
A coupled assay detecting defects in fibroblast isoleucine degradation distal to enoyl-CoA hydratase: application to 3-oxothiolase deficiency
K M Gibson, C F Lee, V Kamali, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1985
Clinical correlation of dysequilibrium syndrome and 4-hydroxybutyric aciduria
K M Gibson, L Sweetman, W L Nyhan, et al.
Journal of Neurogenetics
|
September 1, 1984
Succinic semialdehyde dehydrogenase deficiency
K M Gibson, L Sweetman, W L Nyhan, et al.
Klinische Padiatrie
|
March 1, 1990
[3-hydroxy-3-methylglutaraturia. Clinical aspects, follow-up and therapy in a young child]
E Plöchl, C Bachmann, J P Colombo, et al.
Page
of 19
Search research articles
Search
Showing results (21-30 of 187) with videos related to
Sort By:
Page
of 19
Journal of Inherited Metabolic Disease
|
January 1, 1992
3-Methylglutaconyl-coenzyme-A hydratase deficiency: a new case
K M Gibson, C F Lee, R S Wappner
European Journal of Pediatrics
|
January 1, 1994
Screening for defects of branched-chain amino acid metabolism
K M Gibson, C F Lee, G F Hoffmann
Journal of Virological Methods
|
May 1, 1991
A simple and rapid method for detecting human immunodeficiency virus by PCR
K M Gibson, K A McLean, J P Clewley
Journal of Inherited Metabolic Disease
|
January 1, 1996
beta-Ketothiolase (2-methylacetoacetyl-coenzyme A thiolase) deficiency: identification of two patients in Israel
K M Gibson, O N Elpeleg, M J Bennett
Comparative Biochemistry and Physiology. Part A, Physiology
|
October 1, 1995
gamma-Aminobutyric acid (GABA) metabolism in mammalian neural and nonneural tissues
N J Tillakaratne, L Medina-Kauwe, K M Gibson
Journal of Inherited Metabolic Disease
|
January 1, 1996
Seizures in a boy with succinic semialdehyde dehydrogenase deficiency treated with vigabatrin (gamma-vinyl-GABA)
D Matern, W Lehnert, K M Gibson, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 31, 1992
A coupled assay detecting defects in fibroblast isoleucine degradation distal to enoyl-CoA hydratase: application to 3-oxothiolase deficiency
K M Gibson, C F Lee, V Kamali, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1985
Clinical correlation of dysequilibrium syndrome and 4-hydroxybutyric aciduria
K M Gibson, L Sweetman, W L Nyhan, et al.
Journal of Neurogenetics
|
September 1, 1984
Succinic semialdehyde dehydrogenase deficiency
K M Gibson, L Sweetman, W L Nyhan, et al.
Klinische Padiatrie
|
March 1, 1990
[3-hydroxy-3-methylglutaraturia. Clinical aspects, follow-up and therapy in a young child]
E Plöchl, C Bachmann, J P Colombo, et al.
Page
of 19