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L A Bindoff

Showing results (51-60 of 58) with videos related to

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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.
The Journal of Clinical Investigation|January 1, 1990
Impaired mitochondrial beta-oxidation in a patient with an abnormality of the respiratory chain. Studies in skeletal muscle mitochondriaN J Watmough, L A Bindoff, M A Birch-Machin, et al.
Diabetes Care|November 1, 1995
Insulin and proinsulin secretion in subjects with abnormal glucose tolerance and a mitochondrial tRNA(Leu(UUR)) mutationM Walker, R W Taylor, M W Stewart, et al.
European Journal of Neurology|May 1, 2013
EFNS review on the role of muscle biopsy in the investigation of myalgiaT Kyriakides, C Angelini, J Schaefer, et al.
Annals of Neurology|February 1, 1996
Deficiency of complex II of the mitochondrial respiratory chain in late-onset optic atrophy and ataxiaR W Taylor, M A Birch-Machin, J Schaefer, 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.
Nature Genetics|July 5, 2001
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia diseaseA R Curtis, C Fey, C M Morris, et al.
Brain : a Journal of Neurology|February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutationsP Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
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.
The Journal of Clinical Investigation|January 1, 1990
Impaired mitochondrial beta-oxidation in a patient with an abnormality of the respiratory chain. Studies in skeletal muscle mitochondriaN J Watmough, L A Bindoff, M A Birch-Machin, et al.
Diabetes Care|November 1, 1995
Insulin and proinsulin secretion in subjects with abnormal glucose tolerance and a mitochondrial tRNA(Leu(UUR)) mutationM Walker, R W Taylor, M W Stewart, et al.
European Journal of Neurology|May 1, 2013
EFNS review on the role of muscle biopsy in the investigation of myalgiaT Kyriakides, C Angelini, J Schaefer, et al.
Annals of Neurology|February 1, 1996
Deficiency of complex II of the mitochondrial respiratory chain in late-onset optic atrophy and ataxiaR W Taylor, M A Birch-Machin, J Schaefer, 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.
Nature Genetics|July 5, 2001
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia diseaseA R Curtis, C Fey, C M Morris, et al.
Brain : a Journal of Neurology|February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutationsP Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
Pageof 6