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International Journal of Molecular Sciences
|
October 12, 2019
Assessment of Mitochondrial Dysfunction in Experimental Autoimmune Encephalomyelitis (EAE) Models of Multiple Sclerosis
Xiulin 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 Disease
Mesfer 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 acid
Tomas 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 dystonia
Birgit 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 Acidification
Robert A Heaton, Simon Heales, Khalid Rahman, et al.
The Lancet. Neurology
|
July 23, 2011
The monoamine neurotransmitter disorders: an expanding range of neurological syndromes
Manju 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 hippocampus
Hannah 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 disease
Matthew 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 disease
Lucia Lavalle, Hibba Kurdi, David Moreno Martinez, et al.
Page
of 9
Search research articles
Search
Showing results (11-20 of 82) with videos related to
Sort By:
Page
of 9
International Journal of Molecular Sciences
|
October 12, 2019
Assessment of Mitochondrial Dysfunction in Experimental Autoimmune Encephalomyelitis (EAE) Models of Multiple Sclerosis
Xiulin 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 Disease
Mesfer 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 acid
Tomas 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 dystonia
Birgit 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 Acidification
Robert A Heaton, Simon Heales, Khalid Rahman, et al.
The Lancet. Neurology
|
July 23, 2011
The monoamine neurotransmitter disorders: an expanding range of neurological syndromes
Manju 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 hippocampus
Hannah 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 disease
Matthew 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 disease
Lucia Lavalle, Hibba Kurdi, David Moreno Martinez, et al.
Page
of 9