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K M Gibson

Showing results (11-20 of 187) with videos related to

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Journal of Inherited Metabolic Disease|April 28, 2009
International symposium on pediatric neurotransmitter diseasesK M Gibson, D C De Vivo
Journal of Inherited Metabolic Disease|January 1, 1993
Inherited disorders of GABA metabolismC 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 patientsK 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 acidE 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 metabolismK M Gibson, W L Nyhan, J Jaeken
Lancet (London, England)|November 4, 1989
Vigabatrin therapy in patient with succinic semialdehyde dehydrogenase deficiencyK 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 aciduriaP 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 deficiencyC Yalçinkaya, H Apaydin, S Ozekmekçi, et al.
Pageof 19

Showing results (11-20 of 187) with videos related to

Sort By:
Pageof 19
Journal of Inherited Metabolic Disease|April 28, 2009
International symposium on pediatric neurotransmitter diseasesK M Gibson, D C De Vivo
Journal of Inherited Metabolic Disease|January 1, 1993
Inherited disorders of GABA metabolismC 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 patientsK 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 acidE 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 metabolismK M Gibson, W L Nyhan, J Jaeken
Lancet (London, England)|November 4, 1989
Vigabatrin therapy in patient with succinic semialdehyde dehydrogenase deficiencyK 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 aciduriaP 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 deficiencyC Yalçinkaya, H Apaydin, S Ozekmekçi, et al.
Pageof 19