Keywords: سندرم تخلیه DNA میتوکندریایی; WES; whole exome sequencing; PALF; paediatric acute liver failure; US; United States; MDS; mitochondrial DNA depletion syndrome; WD; Wilson disease; EASL; European Association for the Study of the Liver; CT; computerized tomography; MRI; magnetic resonanc
مقالات ISI سندرم تخلیه DNA میتوکندریایی (ترجمه نشده)
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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.
Keywords: سندرم تخلیه DNA میتوکندریایی; AED; antiepileptic drug; AHS; Alpers-Huttenlocher-syndrome; CNS; central nervous system; COX; Cytochrome-c-oxidase; CPEO; mitochondrial or nuclear chronic progressive external ophthalmoplegia; CSF; cerebro-spinal fluid; EMP; enecephalomyopathy; EP; ence
Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations
Keywords: سندرم تخلیه DNA میتوکندریایی; Mitochondrial DNA depletion syndrome; Myopathy; Thymidine kinase 2; TK2; Mitochondrial myopathy
Clinical and Molecular Characteristics of Mitochondrial DNA Depletion Syndrome Associated with Neonatal Cholestasis and Liver Failure
Keywords: سندرم تخلیه DNA میتوکندریایی; ATP; Adenosine triphosphate; DGUOK; Deoxyguanosine kinase; MDS; Mitochondrial DNA depletion syndrome; MRI; Magnetic resonance imaging; mtDNA; Mitochondrial DNA;
Coenzyme Q10 deficiency in mitochondrial DNA depletion syndromes
Keywords: سندرم تخلیه DNA میتوکندریایی; CoQ; Coenzyme Q10; MDS; mitochondrial DNA depletion syndromes; HPLC; high pressure liquid chromatography; mtDNA; mitochondrial DNA; MRC; mitochondrial respiratory chain; CS; citrate synthase; Mitochondrial DNA depletion syndrome; Coenzyme Q10 deficiency;
Pyruvate therapy for mitochondrial DNA depletion syndrome
Keywords: سندرم تخلیه DNA میتوکندریایی; MDS, mitochondrial DNA depletion syndrome; L/P, lactate-to-pyruvatePyruvate therapy; Mitochondrial DNA depletion syndrome; Mitochondrial diseases; Treatment; Lactate-to-pyruvate ratio; NAD+
Mitochondrial DNA depletion syndromes – Many genes, common mechanisms
Keywords: سندرم تخلیه DNA میتوکندریایی; Mitochondrial DNA; Mitochondrial DNA depletion syndrome; Encephalopathy; Hepatoencephalopathy; Leigh syndrome; Alpers syndrome
The clinical diagnosis of POLG disease and other mitochondrial DNA depletion disorders
Keywords: سندرم تخلیه DNA میتوکندریایی; Mitochondrial disease diagnosis; Mitochondrial DNA depletion syndrome; Alpers–Huttenlocher syndrome; Ataxia-neuropathy spectrum disorders; Progressive external ophthalmoplegia; Childhood myocerebrohepatopathy spectrum; Myoclonic epilepsy myopathy sensory
Progressive myofiber loss with extensive fibro-fatty replacement in a child with mitochondrial DNA depletion syndrome and novel thymidine kinase 2 gene mutations
Keywords: سندرم تخلیه DNA میتوکندریایی; Mitochondrial DNA depletion syndrome; Thymidine kinase 2; Myopathy; Respiratory chain
Fluctuating liver functions in siblings with MPV17 mutations and possible improvement associated with dietary and pharmaceutical treatments targeting respiratory chain complex II
Keywords: سندرم تخلیه DNA میتوکندریایی; MPV17 mutations; Mitochondrial DNA depletion syndrome; Liver dysfunction; Viral infection; Mitochondrial respiratory chain complex; Succinate; Ubiquinone; Ketone milk; Lipid-rich diet; Treatment
The first founder DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome
Keywords: سندرم تخلیه DNA میتوکندریایی; Mitochondrial DNA depletion syndrome; DGUOK gene; Hepatoencephalopathy; Founder mutation; In silico structure analysis;
Case reportGlucose metabolism and diet-based prevention of liver dysfunction in MPV17 mutant patients
Keywords: سندرم تخلیه DNA میتوکندریایی; MDS; mitochondrial DNA depletion syndrome; NNH; Navajo neurohepatopathy; Gamma-GT; gamma-glutamil-transpeptidase; CSF; cerebrospinal fluid; DQ; developmental quotient; IQ; intelligence quotient; MRI; magnetic resonance imaging; EEG; electroencephalogram;
Lack of founder effect for an identical mtDNA depletion syndrome (MDS)-associated MPV17 mutation shared by Navajos and Italians
Keywords: سندرم تخلیه DNA میتوکندریایی; Mitochondrial DNA depletion syndrome; MPV17; Navajo neuro-hepatopathy
Disorders of nuclear-mitochondrial intergenomic signaling
Keywords: سندرم تخلیه DNA میتوکندریایی; mtDNA; mitochondrial DNA; PEO; progressive external ophthalmoplegia; ad; autosomal dominant; ar; autosomal recessive; SANDO; sensory-atactic neuropathy, dysarthria and ophthalmoplegia; SCAE; spino-cerebellar ataxia-epilepsy; TP; thymidine phosphorylase;
Molecular insight into mitochondrial DNA depletion syndrome in two patients with novel mutations in the deoxyguanosine kinase and thymidine kinase 2 genes
Keywords: سندرم تخلیه DNA میتوکندریایی; Deoxyguanosine kinase; Thymidine kinase 2; Mitochondrial DNA depletion; Mitochondrial DNA depletion syndrome; Mutation; Mutagenesis; Enzyme kinetic;