John M. Land
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 13 publications
Blood Mononuclear Cell Mitochondrial Respiratory Chain Complex IV Activity Is Decreased in Multiple Sclerosis Patients: Effects of β-Interferon Treatment.
Journal: Journal of clinical medicine
Published: February 01, 2018
Biochemical diagnosis of coenzyme q10 deficiency.
Journal: Molecular syndromology
Published: August 16, 2014
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2.
Journal: Brain : a journal of neurology
Published: November 21, 2013
Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophy.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: November 08, 2013
Levels of 5-methyltetrahydrofolate and ascorbic acid in cerebrospinal fluid are correlated: implications for the accelerated degradation of folate by reactive oxygen species.
Journal: Neurochemistry international
Published: July 10, 2013
Secondary coenzyme Q10 deficiency and oxidative stress in cultured fibroblasts from patients with riboflavin responsive multiple Acyl-CoA dehydrogenation deficiency.
Journal: Human molecular genetics
Published: June 04, 2013
Assessment of mitochondrial electron transport chain function in a primary astrocyte cell model of hyperhomocystinaemia.
Journal: Toxicology mechanisms and methods
Published: March 08, 2013
Coenzyme Q10 quantification in muscle, fibroblasts and cerebrospinal fluid by liquid chromatography/tandem mass spectrometry using a novel deuterated internal standard.
Journal: Rapid communications in mass spectrometry : RCM
Published: October 17, 2012
Coenzyme Q₁₀ deficiency in mitochondrial DNA depletion syndromes.
Journal: Mitochondrion
Published: October 15, 2012
Genetic dysfunction of MT-ATP6 causes axonal Charcot-Marie-Tooth disease.
Journal: Neurology
Published: August 31, 2012
Last Updated: 09/26/2026