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Journal of Inherited Metabolic Disease
|
April 28, 2009
International symposium on pediatric neurotransmitter diseases
K M Gibson, D C De Vivo
Journal of Inherited Metabolic Disease
|
January 1, 1993
Inherited disorders of GABA metabolism
C Jakobs, J Jaeken, K M Gibson
European Journal of Pediatrics
|
December 1, 1988
3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: review of 18 reported patients
K M Gibson, J Breuer, W L Nyhan
Journal of Inherited Metabolic Disease
|
September 19, 2007
Novel insights into L-2-hydroxyglutaric aciduria: mass isotopomer studies reveal 2-oxoglutaric acid as the metabolic precursor of L-2-hydroxyglutaric acid
E A Struys, K M Gibson, C Jakobs
Journal of Virological Methods
|
June 1, 1993
Detection of HIV-1 in serum, using reverse transcription and the polymerase chain reaction (RT-PCR)
K M Gibson, J Mori, J P Clewley
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology
|
January 1, 1986
Inborn errors of GABA metabolism
K M Gibson, W L Nyhan, J Jaeken
Lancet (London, England)
|
November 4, 1989
Vigabatrin therapy in patient with succinic semialdehyde dehydrogenase deficiency
K M Gibson, D C DeVivo, C Jakobs
Prenatal Diagnosis
|
February 1, 1993
Prenatal detection of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria)
C Jakobs, H Ogier, D Rabier, et al.
Pediatric Research
|
October 1, 1988
Oxidation of [U-14C]succinic semialdehyde in cultured human lymphoblasts: measurement of residual succinic semialdehyde dehydrogenase activity in 11 patients with 4-hydroxybutyric aciduria
P P Pattarelli, W L Nyhan, K M Gibson
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 11, 2001
Delayed-onset dystonia associated with 3-oxothiolase deficiency
C Yalçinkaya, H Apaydin, S Ozekmekçi, et al.
Page
of 19
Search research articles
Search
Showing results (11-20 of 187) with videos related to
Sort By:
Page
of 19
Journal of Inherited Metabolic Disease
|
April 28, 2009
International symposium on pediatric neurotransmitter diseases
K M Gibson, D C De Vivo
Journal of Inherited Metabolic Disease
|
January 1, 1993
Inherited disorders of GABA metabolism
C Jakobs, J Jaeken, K M Gibson
European Journal of Pediatrics
|
December 1, 1988
3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: review of 18 reported patients
K M Gibson, J Breuer, W L Nyhan
Journal of Inherited Metabolic Disease
|
September 19, 2007
Novel insights into L-2-hydroxyglutaric aciduria: mass isotopomer studies reveal 2-oxoglutaric acid as the metabolic precursor of L-2-hydroxyglutaric acid
E A Struys, K M Gibson, C Jakobs
Journal of Virological Methods
|
June 1, 1993
Detection of HIV-1 in serum, using reverse transcription and the polymerase chain reaction (RT-PCR)
K M Gibson, J Mori, J P Clewley
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology
|
January 1, 1986
Inborn errors of GABA metabolism
K M Gibson, W L Nyhan, J Jaeken
Lancet (London, England)
|
November 4, 1989
Vigabatrin therapy in patient with succinic semialdehyde dehydrogenase deficiency
K M Gibson, D C DeVivo, C Jakobs
Prenatal Diagnosis
|
February 1, 1993
Prenatal detection of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria)
C Jakobs, H Ogier, D Rabier, et al.
Pediatric Research
|
October 1, 1988
Oxidation of [U-14C]succinic semialdehyde in cultured human lymphoblasts: measurement of residual succinic semialdehyde dehydrogenase activity in 11 patients with 4-hydroxybutyric aciduria
P P Pattarelli, W L Nyhan, K M Gibson
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 11, 2001
Delayed-onset dystonia associated with 3-oxothiolase deficiency
C Yalçinkaya, H Apaydin, S Ozekmekçi, et al.
Page
of 19