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G N Thompson

Showing results (41-50 of 63) with videos related to

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Human Genetics|January 1, 1995
A topoisomerase II cleavage site is associated with a novel mitochondrial DNA deletionR B Blok, D R Thorburn, G N Thompson, et al.
Archives of Disease in Childhood|September 1, 1987
Type V hyperlipoproteinaemia in neonatesG N Thompson, A J Knight, I H Craig, et al.
Lancet (London, England)|June 10, 1989
Contribution of aminoacid catabolism to propionate production in methylmalonic acidaemiaJ H Walter, G N Thompson, J V Leonard, et al.
European Journal of Clinical Investigation|December 1, 1988
Relationships between plasma isotope enrichments of leucine and alpha-ketoisocaproic acid during continuous infusion of labelled leucineG N Thompson, P J Pacy, G C Ford, et al.
The New England Journal of Medicine|October 23, 1997
Fasting hypoketotic coma in a child with deficiency of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthaseG N Thompson, B Y Hsu, J J Pitt, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 30, 1989
Measurement of propionate turnover in vivo using sodium [2H5]propionate and sodium [13C]propionateJ H Walter, G N Thompson, J V Leonard, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
In vivo disposal of phenylalanine in phenylketonuria: a study of two siblingsE Treacy, J J Pitt, K Seller, et al.
Clinical and Experimental Neurology|January 1, 1987
Acute encephalopathy following petrol sniffing in two aboriginal patientsR H Rischbieth, G N Thompson, A Hamilton-Bruce, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Production and disposal of medium-chain fatty acids in children with medium-chain acyl-CoA dehydrogenase deficiencyS J Heales, G N Thompson, A F Massoud, et al.
The Medical Journal of Australia|July 7, 1986
Management and outcome of children with congenital hypothyroidism detected on neonatal screening in South AustraliaG N Thompson, R B McCrossin, J L Penfold, et al.
Pageof 7

Showing results (41-50 of 63) with videos related to

Sort By:
Pageof 7
Human Genetics|January 1, 1995
A topoisomerase II cleavage site is associated with a novel mitochondrial DNA deletionR B Blok, D R Thorburn, G N Thompson, et al.
Archives of Disease in Childhood|September 1, 1987
Type V hyperlipoproteinaemia in neonatesG N Thompson, A J Knight, I H Craig, et al.
Lancet (London, England)|June 10, 1989
Contribution of aminoacid catabolism to propionate production in methylmalonic acidaemiaJ H Walter, G N Thompson, J V Leonard, et al.
European Journal of Clinical Investigation|December 1, 1988
Relationships between plasma isotope enrichments of leucine and alpha-ketoisocaproic acid during continuous infusion of labelled leucineG N Thompson, P J Pacy, G C Ford, et al.
The New England Journal of Medicine|October 23, 1997
Fasting hypoketotic coma in a child with deficiency of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthaseG N Thompson, B Y Hsu, J J Pitt, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 30, 1989
Measurement of propionate turnover in vivo using sodium [2H5]propionate and sodium [13C]propionateJ H Walter, G N Thompson, J V Leonard, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
In vivo disposal of phenylalanine in phenylketonuria: a study of two siblingsE Treacy, J J Pitt, K Seller, et al.
Clinical and Experimental Neurology|January 1, 1987
Acute encephalopathy following petrol sniffing in two aboriginal patientsR H Rischbieth, G N Thompson, A Hamilton-Bruce, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Production and disposal of medium-chain fatty acids in children with medium-chain acyl-CoA dehydrogenase deficiencyS J Heales, G N Thompson, A F Massoud, et al.
The Medical Journal of Australia|July 7, 1986
Management and outcome of children with congenital hypothyroidism detected on neonatal screening in South AustraliaG N Thompson, R B McCrossin, J L Penfold, et al.
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