V. Neergheen

发表

Coenzyme Q10 prevents hepatic fibrosis, inflammation, and oxidative stress in a male rat model of poor maternal nutrition and accelerated postnatal growth1

C. Aiken, S. Ozanne, I. Hargreaves, 2015, The American journal of clinical nutrition.

Coenzyme Q 10 prevents hepatic fibrosis , inflammation , and oxidative stress in a male rat model of poor maternal nutrition and accelerated postnatal growth 1

C. Aiken, S. Ozanne, I. Hargreaves, 2016 .

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

J. Holton, H. Houlden, I. Hargreaves, 2016, PloS one.

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

C. Aiken, S. Ozanne, I. Hargreaves, 2016, Disease Models & Mechanisms.

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

P. Navas, R. Artuch, I. Hargreaves, 2015, BioFactors.

Missense dopamine transporter mutations associate with adult parkinsonism and ADHD.

Thorvald F. Andreassen, H. Weinstein, H. Sitte, 2014, The Journal of clinical investigation.

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

M. Singer, M. Bauer, J. Backman, 2017, Clinical science.

Measurement of plasma B6 vitamer profiles in children with inborn errors of vitamin B6 metabolism using an LC-MS/MS method

K. Mills, P. Clayton, S. Heales, 2013, Journal of Inherited Metabolic Disease.

Pyridoxal 5′‐phosphate deficiency causes a loss of aromatic l‐amino acid decarboxylase in patients and human neuroblastoma cells, implications for aromatic l‐amino acid decarboxylase and vitamin B6 deficiency states

P. Clayton, P. Clayton, J. Fitzgerald, 2010, Journal of neurochemistry.

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

P. Navas, E. Ruiz-Pesini, E. Trevisson, 2016, Mitochondrion.

Spectrum of movement disorders and neurotransmitter abnormalities in paediatric POLG disease

M. King, M. Kurian, E. Meyer, 2018, Journal of Inherited Metabolic Disease.

Levels of 5-methyltetrahydrofolate and ascorbic acid in cerebrospinal fluid are correlated: Implications for the accelerated degradation of folate by reactive oxygen species

S. Rahman, S. Heales, S. Eaton, 2013, Neurochemistry International.

Statin and Fibrate‐Induced Dichotomy of Mitochondrial Function

A. Dyson, I. Hargreaves, V. Neergheen, 2018 .

Plasma coenzyme Q10 status is impaired in selected genetic conditions

Eduardo Ruiz-Pesini, Julio Montoya, Rafael Artuch, 2019, Scientific Reports.

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

Z. Tümer, I. Hargreaves, T. Nielsen, 2017, Mitochondrion.

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

P. Navas, P. Clayton, R. Artuch, 2015, JIMD reports.

Coenzyme Q10 in the Treatment of Mitochondrial Disease

R. Artuch, I. Hargreaves, V. Neergheen, 2017 .

Plasma coenzyme Q10 status is impaired in selected genetic conditions

P. Navas, E. Ruiz-Pesini, R. Artuch, 2019, Scientific Reports.

SPECIAL COLLECTION : TRANSLATIONAL IMPACT OF RAT Poor maternal nutrition and accelerated postnatal growth induces an accelerated aging phenotype and oxidative stress in skeletal muscle of male rats

C. Aiken, S. Ozanne, I. Hargreaves, 2016 .