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Simon Heales

Showing results (11-20 of 82) with videos related to

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International Journal of Molecular Sciences|October 12, 2019
Assessment of Mitochondrial Dysfunction in Experimental Autoimmune Encephalomyelitis (EAE) Models of Multiple SclerosisXiulin Ng, Mona Sadeghian, Simon Heales, et al.
Journal of Clinical Medicine|October 28, 2017
Oxidative Stress: Mechanistic Insights into Inherited Mitochondrial Disorders and Parkinson's DiseaseMesfer Al Shahrani, Simon Heales, Iain Hargreaves, et al.
Journal of Neurochemistry|July 17, 2024
SH-SY5Y cells undergo changes in peroxisomal metabolism when exposed to decanoic acidTomas Baldwin, Peter Clayton, Tricia Rutherford, et al.
Pediatric Research|June 27, 2002
Selective decrease in central nervous system serotonin turnover in children with dopa-nonresponsive dystoniaBirgit Assmann, Martin Köhler, Georg F Hoffmann, et al.
Journal of the Neurological Sciences|May 8, 2020
Cerebrospinal fluid folate, ascorbate, and tetrahydrobiopterin deficiency in superficial siderosis: A new potential mechanism of neurological dysfunction?Jack Belsten, David J Werring, Howell Jones, et al.
Journal of Clinical Medicine|June 25, 2020
The Effect of Cellular Coenzyme Q<sub>10</sub> Deficiency on Lysosomal AcidificationRobert A Heaton, Simon Heales, Khalid Rahman, et al.
The Lancet. Neurology|July 23, 2011
The monoamine neurotransmitter disorders: an expanding range of neurological syndromesManju A Kurian, Paul Gissen, Martin Smith, et al.
Neurochemistry International|November 18, 2005
Depletion of reduced glutathione precedes inactivation of mitochondrial enzymes following limbic status epilepticus in the rat hippocampusHannah Sleven, Julie E Gibbs, Simon Heales, et al.
Molecular Genetics and Metabolism|June 24, 2018
Impact of sphingolipids on osteoblast and osteoclast activity in Gaucher diseaseMatthew C Reed, Capucine Schiffer, Simon Heales, et al.
Orphanet Journal of Rare Diseases|July 1, 2026
Mitochondrial stress markers associate with phenotypic variability in Fabry diseaseLucia Lavalle, Hibba Kurdi, David Moreno Martinez, et al.
Pageof 9

Showing results (11-20 of 82) with videos related to

Sort By:
Pageof 9
International Journal of Molecular Sciences|October 12, 2019
Assessment of Mitochondrial Dysfunction in Experimental Autoimmune Encephalomyelitis (EAE) Models of Multiple SclerosisXiulin Ng, Mona Sadeghian, Simon Heales, et al.
Journal of Clinical Medicine|October 28, 2017
Oxidative Stress: Mechanistic Insights into Inherited Mitochondrial Disorders and Parkinson's DiseaseMesfer Al Shahrani, Simon Heales, Iain Hargreaves, et al.
Journal of Neurochemistry|July 17, 2024
SH-SY5Y cells undergo changes in peroxisomal metabolism when exposed to decanoic acidTomas Baldwin, Peter Clayton, Tricia Rutherford, et al.
Pediatric Research|June 27, 2002
Selective decrease in central nervous system serotonin turnover in children with dopa-nonresponsive dystoniaBirgit Assmann, Martin Köhler, Georg F Hoffmann, et al.
Journal of the Neurological Sciences|May 8, 2020
Cerebrospinal fluid folate, ascorbate, and tetrahydrobiopterin deficiency in superficial siderosis: A new potential mechanism of neurological dysfunction?Jack Belsten, David J Werring, Howell Jones, et al.
Journal of Clinical Medicine|June 25, 2020
The Effect of Cellular Coenzyme Q<sub>10</sub> Deficiency on Lysosomal AcidificationRobert A Heaton, Simon Heales, Khalid Rahman, et al.
The Lancet. Neurology|July 23, 2011
The monoamine neurotransmitter disorders: an expanding range of neurological syndromesManju A Kurian, Paul Gissen, Martin Smith, et al.
Neurochemistry International|November 18, 2005
Depletion of reduced glutathione precedes inactivation of mitochondrial enzymes following limbic status epilepticus in the rat hippocampusHannah Sleven, Julie E Gibbs, Simon Heales, et al.
Molecular Genetics and Metabolism|June 24, 2018
Impact of sphingolipids on osteoblast and osteoclast activity in Gaucher diseaseMatthew C Reed, Capucine Schiffer, Simon Heales, et al.
Orphanet Journal of Rare Diseases|July 1, 2026
Mitochondrial stress markers associate with phenotypic variability in Fabry diseaseLucia Lavalle, Hibba Kurdi, David Moreno Martinez, et al.
Pageof 9