标题
Coenzyme Q deficiency in muscle
作者
关键词
-
出版物
CURRENT OPINION IN NEUROLOGY
Volume 24, Issue 5, Pages 449-456
出版商
Ovid Technologies (Wolters Kluwer Health)
发表日期
2011-10-05
DOI
10.1097/wco.0b013e32834ab528
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Expression of the human atypical kinase ADCK3 rescues coenzyme Q biosynthesis and phosphorylation of Coq polypeptides in yeast coq8 mutants
- (2011) Letian X. Xie et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
- COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
- (2011) Saskia F. Heeringa et al. JOURNAL OF CLINICAL INVESTIGATION
- Subacute myopathy in a mature patient due to multiple acyl-coenzyme a dehydrogenase deficiency
- (2011) Pierre Kaminsky et al. MUSCLE & NERVE
- Mitochondrial dysfunction in skin biopsies and blood mononuclear cells from two cases of fibromyalgia patients
- (2010) Mario D. Cordero et al. CLINICAL BIOCHEMISTRY
- Evidence-Based Management of Statin Myopathy
- (2010) Charles R. Harper et al. Current Atherosclerosis Reports
- Reactive oxygen species, oxidative stress, and cell death correlate with level of CoQ10 deficiency
- (2010) Catarina M. Quinzii et al. FASEB JOURNAL
- Rosuvastatin Lowers Coenzyme Q10 Levels, but not Mitochondrial Adenosine Triphosphate Synthesis, in Children with Familial Hypercholesterolemia
- (2010) Hans J. Avis et al. JOURNAL OF PEDIATRICS
- Treatment of CoQ10 Deficient Fibroblasts with Ubiquinone, CoQ Analogs, and Vitamin C: Time- and Compound-Dependent Effects
- (2010) Luis C. López et al. PLoS One
- A Nonsense Mutation in COQ9 Causes Autosomal-Recessive Neonatal-Onset Primary Coenzyme Q10 Deficiency: A Potentially Treatable Form of Mitochondrial Disease
- (2009) Andrew J. Duncan et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Coenzyme Q deficiency triggers mitochondria degradation by mitophagy
- (2009) Ángeles Rodríguez-Hernández et al. Autophagy
- Human CoQ10deficiencies
- (2009) C. M. Quinzii et al. BIOFACTORS
- Coenzyme Q10 is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduria
- (2009) D. Haas et al. JOURNAL OF INHERITED METABOLIC DISEASE
- ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency
- (2009) Wen-Chen Liang et al. NEUROMUSCULAR DISORDERS
- Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy
- (2009) Sabrina Sacconi et al. NEUROMUSCULAR DISORDERS
- ADCK3, an Ancestral Kinase, Is Mutated in a Form of Recessive Ataxia Associated with Coenzyme Q10 Deficiency
- (2008) Clotilde Lagier-Tourenne et al. AMERICAN JOURNAL OF HUMAN GENETICS
- CABC1 Gene Mutations Cause Ubiquinone Deficiency with Cerebellar Ataxia and Seizures
- (2008) Julie Mollet et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Functional characterization of human COQ4, a gene required for Coenzyme Q10 biosynthesis
- (2008) Alberto Casarin et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Analysis of Coenzyme Q10 in muscle and fibroblasts for the diagnosis of CoQ10 deficiency syndromes
- (2008) Raquel Montero et al. CLINICAL BIOCHEMISTRY
- Coenzyme Q10 deficiency associated with a mitochondrial DNA depletion syndrome: A case report
- (2008) Raquel Montero et al. CLINICAL BIOCHEMISTRY
- Coenzyme Q10 distribution in blood is altered in patients with Fibromyalgia
- (2008) M.D. Cordero et al. CLINICAL BIOCHEMISTRY
- Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiency
- (2008) Catarina M. Quinzii et al. FASEB JOURNAL
- Systematic evaluation of muscle coenzyme Q10 content in children with mitochondrial respiratory chain enzyme deficiencies
- (2008) Michael V. Miles et al. MITOCHONDRION
- Early Coenzyme Q10 Supplementation in Primary Coenzyme Q10 Deficiency
- (2008) Giovanni Montini et al. NEW ENGLAND JOURNAL OF MEDICINE
- Primary Coenzyme Q Deficiency in Pdss2 Mutant Mice Causes Isolated Renal Disease
- (2008) Min Peng et al. PLoS Genetics
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