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