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A A Morris

Showing results (41-50 of 52) with videos related to

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Archives of Disease in Childhood|January 31, 2006
Glucose and leucine kinetics in idiopathic ketotic hypoglycaemiaO A Bodamer, K Hussein, A A Morris, et al.
Annals of Neurology|September 1, 1996
MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNAR W Taylor, P F Chinnery, F Haldane, et al.
Human Molecular Genetics|June 1, 1997
Molecular mechanisms in mitochondrial DNA depletion syndromeJ W Taanman, A G Bodnar, J M Cooper, et al.
Archives of Disease in Childhood|October 23, 2001
ARC syndrome: an expanding range of phenotypesK M Eastham, P J McKiernan, D V Milford, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Impaired ketogenesis in fructose-1,6-bisphosphatase deficiency: a pitfall in the investigation of hypoglycaemiaA A Morris, S Deshphande, M P Ward-Platt, et al.
Journal of Child Neurology|September 1, 1996
Respiratory chain dysfunction in progressive neuronal degeneration of childhood with liver diseaseA A Morris, R Singh-Kler, R H Perry, et al.
Pediatric Nephrology (Berlin, Germany)|August 1, 1995
Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chainA A Morris, R W Taylor, M A Birch-Machin, et al.
Journal of Hepatology|May 5, 1998
Liver failure associated with mitochondrial DNA depletionA A Morris, J W Taanman, J Blake, et al.
The Journal of Pharmacology and Experimental Therapeutics|March 1, 1981
Effect of N-[(S)-1-carboxy-3-phenylpropyl]-L-Ala-L-Pro and its ethyl ester (MK-421) on angiotensin converting enzyme in vitro and angiotensin I pressor responses in vivoD M Gross, C S Sweet, E H Ulm, et al.
Annals of Neurology|July 1, 1996
Deficiency of respiratory chain complex I is a common cause of Leigh diseaseA A Morris, J V Leonard, G K Brown, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Archives of Disease in Childhood|January 31, 2006
Glucose and leucine kinetics in idiopathic ketotic hypoglycaemiaO A Bodamer, K Hussein, A A Morris, et al.
Annals of Neurology|September 1, 1996
MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNAR W Taylor, P F Chinnery, F Haldane, et al.
Human Molecular Genetics|June 1, 1997
Molecular mechanisms in mitochondrial DNA depletion syndromeJ W Taanman, A G Bodnar, J M Cooper, et al.
Archives of Disease in Childhood|October 23, 2001
ARC syndrome: an expanding range of phenotypesK M Eastham, P J McKiernan, D V Milford, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Impaired ketogenesis in fructose-1,6-bisphosphatase deficiency: a pitfall in the investigation of hypoglycaemiaA A Morris, S Deshphande, M P Ward-Platt, et al.
Journal of Child Neurology|September 1, 1996
Respiratory chain dysfunction in progressive neuronal degeneration of childhood with liver diseaseA A Morris, R Singh-Kler, R H Perry, et al.
Pediatric Nephrology (Berlin, Germany)|August 1, 1995
Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chainA A Morris, R W Taylor, M A Birch-Machin, et al.
Journal of Hepatology|May 5, 1998
Liver failure associated with mitochondrial DNA depletionA A Morris, J W Taanman, J Blake, et al.
The Journal of Pharmacology and Experimental Therapeutics|March 1, 1981
Effect of N-[(S)-1-carboxy-3-phenylpropyl]-L-Ala-L-Pro and its ethyl ester (MK-421) on angiotensin converting enzyme in vitro and angiotensin I pressor responses in vivoD M Gross, C S Sweet, E H Ulm, et al.
Annals of Neurology|July 1, 1996
Deficiency of respiratory chain complex I is a common cause of Leigh diseaseA A Morris, J V Leonard, G K Brown, et al.
Pageof 6