A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiency.
about
Isolation and functional expression of human COQ3, a gene encoding a methyltransferase required for ubiquinone biosynthesisA mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiencyStatin adverse effects : a review of the literature and evidence for a mitochondrial mechanismA nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial diseasePrenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disordersCoenzyme Q and Its Role in the Dietary Therapy against AgingA novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13.Age-related alterations in oxidatively damaged proteins of mouse skeletal muscle mitochondrial electron transport chain complexes.The in-depth evaluation of suspected mitochondrial diseaseClinical presentations of coenzyme q10 deficiency syndromeBiochemical diagnosis of coenzyme q10 deficiency.Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutationsConceptual foundations of the UCSD Statin Study: a randomized controlled trial assessing the impact of statins on cognition, behavior, and biochemistry.Mutations in coenzyme Q10 biosynthetic genes.CoQ10 deficiency diseases in adults.Age-related increases in oxidatively damaged proteins of mouse kidney mitochondrial electron transport chain complexesEffects of acute and 14-day coenzyme Q10 supplementation on exercise performance in both trained and untrained individualsHuman coenzyme Q10 deficiencyHeterogeneity of coenzyme Q10 deficiency: patient study and literature review.Coenzyme Q10: is there a clinical role and a case for measurement?Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiency.Coenzyme Q10 prevents accelerated cardiac aging in a rat model of poor maternal nutrition and accelerated postnatal growth.Coenzyme Q10 deficiencies in neuromuscular diseases.Therapeutic use of coenzyme Q10 and coenzyme Q10-related compounds and formulations.Coenzyme Q and mitochondrial diseasePrimary and secondary CoQ(10) deficiencies in humans.Primary coenzyme Q10 (CoQ 10) deficiencies and related nephropathies.Human CoQ10 deficienciesApolipoprotein A1 regulates coenzyme Q10 absorption, mitochondrial function, and infarct size in a mouse model of myocardial infarction.A randomized trial of coenzyme Q10 in mitochondrial disorders.A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C-methyltransferase deficiency.Statin-associated adverse cognitive effects: survey results from 171 patients.Pediatric reference intervals for muscle coenzyme Q(10).Mitochondrial Diseases as Model of Neurodegeneration.
P2860
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P2860
A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiency.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
A case of mitochondrial enceph ...... uscle coenzyme Q10 deficiency.
@en
type
label
A case of mitochondrial enceph ...... uscle coenzyme Q10 deficiency.
@en
prefLabel
A case of mitochondrial enceph ...... uscle coenzyme Q10 deficiency.
@en
P2093
P1476
A case of mitochondrial enceph ...... muscle coenzyme Q10 deficiency
@en
P2093
C Charpentier
D François
I Desguerre
P356
10.1016/S0022-510X(98)00006-9
P50
P577
1998-01-01T00:00:00Z