Viruna Neergheen

Queen Square
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 14 publications

Correction to: Spectrum of movement disorders and neurotransmitter abnormalities in paediatric POLG disease.

Correction to: Spectrum of movement disorders and neurotransmitter abnormalities in paediatric POLG disease.

Journal: Journal of inherited metabolic disease
Published: November 21, 2018

Plasma coenzyme Q10 status is impaired in selected genetic conditions.

Plasma coenzyme Q10 status is impaired in selected genetic conditions.

Journal: Scientific reports
Published: June 26, 2018

Spectrum of movement disorders and neurotransmitter abnormalities in paediatric POLG disease.

Spectrum of movement disorders and neurotransmitter abnormalities in paediatric POLG disease.

Journal: Journal of inherited metabolic disease
Published: March 29, 2018

Simvastatin pre-treatment improves survival and mitochondrial function in a 3-day fluid-resuscitated rat model of sepsis.

Simvastatin pre-treatment improves survival and mitochondrial function in a 3-day fluid-resuscitated rat model of sepsis.

Journal: Clinical science (London, England : 1979)
Published: November 09, 2016

Evidence of oxidative stress and mitochondrial dysfunction in spinocerebellar ataxia type 2 (SCA2) patient fibroblasts: Effect of coenzyme Q10 supplementation on these parameters.

Evidence of oxidative stress and mitochondrial dysfunction in spinocerebellar ataxia type 2 (SCA2) patient fibroblasts: Effect of coenzyme Q10 supplementation on these parameters.

Journal: Mitochondrion
Published: October 06, 2016

Poor maternal nutrition and accelerated postnatal growth induces an accelerated aging phenotype and oxidative stress in skeletal muscle of male rats.

Poor maternal nutrition and accelerated postnatal growth induces an accelerated aging phenotype and oxidative stress in skeletal muscle of male rats.

Journal: Disease models & mechanisms
Published: June 16, 2016

Secondary coenzyme Q10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders.

Secondary coenzyme Q10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders.

Journal: Mitochondrion
Published: March 10, 2016

Coenzyme Q10 Levels Are Decreased in the Cerebellum of Multiple-System Atrophy Patients.

Coenzyme Q10 Levels Are Decreased in the Cerebellum of Multiple-System Atrophy Patients.

Journal: PloS one
Published: September 21, 2015

Determination of urinary coenzyme Q10 by HPLC with electrochemical detection: Reference values for a paediatric population.

Determination of urinary coenzyme Q10 by HPLC with electrochemical detection: Reference values for a paediatric population.

Journal: BioFactors (Oxford, England)
Published: August 04, 2015

Coenzyme Q10 prevents hepatic fibrosis, inflammation, and oxidative stress in a male rat model of poor maternal nutrition and accelerated postnatal growth.

Coenzyme Q10 prevents hepatic fibrosis, inflammation, and oxidative stress in a male rat model of poor maternal nutrition and accelerated postnatal growth.

Journal: The American journal of clinical nutrition
Published: July 28, 2015

Coenzyme Q10 and Pyridoxal Phosphate Deficiency Is a Common Feature in Mucopolysaccharidosis Type III.

Coenzyme Q10 and Pyridoxal Phosphate Deficiency Is a Common Feature in Mucopolysaccharidosis Type III.

Journal: JIMD reports
Published: December 04, 2014

Missense dopamine transporter mutations associate with adult parkinsonism and ADHD.

Missense dopamine transporter mutations associate with adult parkinsonism and ADHD.

Journal: The Journal of clinical investigation
Published: October 18, 2013
Showing 1-12 of 14

Last Updated: 09/26/2026