Keywords: انسفالومیوپاتی; Mitochondrial diseases; Encephalomyopathy; Lactic acidosis; Nitric oxide deficiency; Arginine; Citrulline; Angiopathy; Endothelial dysfunction;
مقالات ISI انسفالومیوپاتی (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Identification of homocysteine-suppressive mitochondrial ETC complex genes and tissue expression profile - Novel hypothesis establishment
Keywords: انسفالومیوپاتی; Bet; betaine; BM; bone marrow; C. elegans; caenorhabditis elegans; CBS; cystathionine-β-synthase; CELMP; cardioencephalomyopathy; Cho; choline; CSE; cystathionineγ-lyase; CT; connective tissue; Cysta; cystathionine; D; days; DCC; dog cardiac cells; DD;
Novel recessive mutations in COQ4 cause severe infantile cardiomyopathy and encephalopathy associated with CoQ10 deficiency
Keywords: انسفالومیوپاتی; CoQ10 deficiency; CoQ4; Infantile cardiomyopathy; Encephalomyopathy; Whole exome sequencing;
Five novel SUCLG1 mutations in three Chinese patients with succinate-CoA ligase deficiency noticed by mild methylmalonic aciduria
Keywords: انسفالومیوپاتی; Methylmalonic aciduria; Succinate-CoA ligase deficiency; Encephalomyopathy; Mitochondrial DNA depletion; SUCLG1
Obstetric complications in carriers of the m.3243AÂ >Â G mutation, a retrospective cohort study on maternal and fetal outcome
Keywords: انسفالومیوپاتی; m.3243AÂ >Â G mutation; Mitochondrial myopathy; Encephalomyopathy; Lactic acidosis and stroke-like episodes (MELAS syndrome); Maternally inherited diabetes deafness (MIDD); Mitochondrial medicine; Preeclampsia; Diabetes gravidarum; Prematurity; Dysmaturit
Mitochondrial encephalomyopathy with cytochrome c oxidase deficiency caused by a novel mutation in the MTCO1 gene
Keywords: انسفالومیوپاتی; Encephalomyopathy; Mitochondrial DNA; Cytochrome c oxidase; MTCO1;
A novel homozygous mutation in SUCLA2 gene identified by exome sequencing
Keywords: انسفالومیوپاتی; MDS; mtDNA depletion syndrome; MMA; methylmalonic acid; MRC; mitochondrial respiratory chain; mtDNA; mitochondrial DNA; NGS; next-generation sequencing; OXPHOS; oxidative phosphorylation; Mitochondrial disorder; Encephalomyopathy; Mitochondrial DNA deplet
Modeling mitochondrial encephalomyopathy in Drosophila
Keywords: انسفالومیوپاتی; Drosophila; mtATP6; Mitochondria; mtCoI; mtND2; Encephalomyopathy;
Treatment of mitochondrial disorders
Keywords: انسفالومیوپاتی; Respiratory chain; Oxidative phosphorylation; Encephalomyopathy; Mitochondriopathy; Mitochondrial cytopathy; Cerebrum; Brain; Spinal cord; Multi-system diseaseAHS, Alpers Huttenlocher syndrome; ATP, adenosine-tri-phosphate; CCT, cerebral computed tomograp
Laminar cortical necrosis in mitochondrial disorders
Keywords: انسفالومیوپاتی; Respiratory chain; Oxidative phosphorylation; Encephalomyopathy; Mitochondriopathy; Mitochondrial cytopathy; Cerebrum; Brain; Imaging; Cerebral magnetic resonance imaging; Autopsy; Cortex
Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patient
Keywords: انسفالومیوپاتی; Mitochondria; OXPHOS disorders; Encephalomyopathy; BCS1L; Assembly;
A novel mutation of the RRM2B gene in an infant with early fatal encephalomyopathy, central hypomyelination, and tubulopathy
Keywords: انسفالومیوپاتی; RRM2B-mutation; Infant; Encephalomyopathy; Central hypomyelination; Tubulopathy
Complex I deficiency in Persian multiple sclerosis patients
Keywords: انسفالومیوپاتی; Multiple sclerosis; Mitochondrial complex I; Encephalomyopathy; Mitochondrial DNA; Spectrophotometry;
Mitochondrial neuropathy
Keywords: انسفالومیوپاتی; Respiratory chain; Neuromuscular disorder; Encephalomyopathy; Metabolic disorder; Lactacidosis;