27 results on '"Neergheen, Viruna"'
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2. Plasma coenzyme Q10 status is impaired in selected genetic conditions
3. Coenzyme Q10 prevents hepatic fibrosis, inflammation, and oxidative stress in a male rat model of poor maternal nutrition and accelerated postnatal growth
4. Statin and Fibrate-Induced Dichotomy of Mitochondrial Function
5. Levels of 5-methyltetrahydrofolate and ascorbic acid in cerebrospinal fluid are correlated: Implications for the accelerated degradation of folate by reactive oxygen species
6. Abnormalities of CSF Neurotransmitters/Folates
7. Missense dopamine transporter mutations associate with adult parkinsonism and ADHD
8. Coenzyme Q10 and Pyridoxal Phosphate Deficiency Is a Common Feature in Mucopolysaccharidosis Type III
9. Determination of urinary coenzyme Q10 by HPLC with electrochemical detection: Reference values for a paediatric population
10. Measurement of plasma B6 vitamer profiles in children with inborn errors of vitamin B6 metabolism using an LC-MS/MS method
11. 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
12. Poor maternal nutrition and accelerated postnatal growth induces an accelerated aging phenotype and oxidative stress in skeletal muscle of male rats
13. Coenzyme Q10 prevents hepatic fibrosis, inflammation, and oxidative stress in a male rat model of poor maternal nutrition and accelerated postnatal growth1
14. Evidence of oxidative stress and mitochondrial dysfunction in spinocerebellar ataxia type 2 (SCA2) patient fibroblasts: Effect of coenzyme Q10 supplementation on these parameters
15. Simvastatin pre-treatment improves survival and mitochondrial function in a 3-day fluid-resuscitated rat model of sepsis
16. Coenzyme Q10 in the Treatment of Mitochondrial Disease
17. Secondary coenzyme Q 10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders
18. Coenzyme Q10 Levels Are Decreased in the Cerebellum of Multiple-System Atrophy Patients
19. Determination of urinary coenzyme Q10by HPLC with electrochemical detection: Reference values for a paediatric population
20. Coenzyme Q10 levels are reduced in the cerebellum of multiple system atrophy patients (P1.182)
21. Coenzyme Q10 prevents hepatic fibrosis, inflammation, and oxidative stress in a male rat model of poor maternal nutrition and accelerated postnatal growth.
22. Determination of urinary coenzyme Q10 by HPLC with electrochemical detection: Reference values for a paediatric population.
23. Measurement of plasma B 6 vitamer profiles in children with inborn errors of vitamin B 6 metabolism using an LC‐MS/MS method
24. 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.
25. Plasma coenzyme Q10 status is impaired in selected genetic conditions.
26. Coenzyme Q10in the Treatment of Mitochondrial Disease
27. Secondary coenzyme Q10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders.
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