Keywords: نورروپاتی اپتیکی ارثی Leber; Respiratory complex I; Xenobiotic; Mitochondrial DNA; Leber hereditary optic neuropathy; Gene-environment interaction;
مقالات ISI نورروپاتی اپتیکی ارثی Leber (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: نورروپاتی اپتیکی ارثی Leber; Optic nerve; Second cranial nerve; Optic neuropathy; mtDNA; Oxidative phosphorylation; Mitochondrial; Respiratory chain; ADOA; Autosomal dominant optic atrophy; AION; Anterior ischemic optic neuropathy; AROA; Autosomal recessive optic atrophy; ATP; Adenos
Keywords: نورروپاتی اپتیکی ارثی Leber; Annual incidence; Gender proportion; Leber hereditary optic neuropathy; Mitochondrial DNA; Penetrance;
Keywords: نورروپاتی اپتیکی ارثی Leber; leber hereditary optic neuropathy; depression; adaptation, psychologic; adjustment disorders; blindness; vision disorders; Kupfer curve.;
Keywords: نورروپاتی اپتیکی ارثی Leber; optic neuropathy; mitochondria; retinal ganglion cells; Leber hereditary optic neuropathy; nutritional deficiencies; neuropatÃa óptica; mitocondria; células ganglionares de la retina; NeuropatÃa Ãptica Hereditaria de Leber; deficiencias nutricionales
Keywords: نورروپاتی اپتیکی ارثی Leber; AD; autosomal dominant; ADNIV; autosomal dominant neovascular inflammatory vitreoretinopathy; AR; autosomal recessive; AR-1; autosomal recessive-1 allele identified; ARMS; amplification refractory mutation system; AZOOR; acute zonal occult outer retinopat
Keywords: نورروپاتی اپتیکی ارثی Leber; optic neuropathy; genetic visual loss; mitochondrial disease; Leber hereditary optic neuropathy; deafness and diabetes
Keywords: نورروپاتی اپتیکی ارثی Leber; Mitochondrial disease; Oxidative stress; Friedreich ataxia; Leber hereditary optic neuropathy; Leigh syndrome; MELAS; MERRF; Inflammation; Neurodegeneration; Neuroinflammation; Free radicals;
Keywords: نورروپاتی اپتیکی ارثی Leber; ADEM; acute demyelinating encephalomyelitis; AION; anterior ischaemic optic neuropathy; AQP4; aquaporin-4; AZOOR; acute zonal occult outer retinopathy; CF; count fingers; CRION; chronic relapsing inflammatory optic neuropathy; CSF; cerebrospinal fluid; CT
Keywords: نورروپاتی اپتیکی ارثی Leber; Mitochondria; Mitochondrial diseases; Neurodegenerative disorders; Pharmacological neuroprotection; Mitochondrie; Maladies mitochondriales; Maladies neurodégénératives; Neuroprotection pharmacologique; AD; Alzheimer's disease; AICAR; 5-aminoimidazole-4
Keywords: نورروپاتی اپتیکی ارثی Leber; Wolfram Syndrome; Leber hereditary optic neuropathy; Optic nerve; Retinal ganglion cell; Axonal degeneration; Myelin basic protein;
Keywords: نورروپاتی اپتیکی ارثی Leber; RGC; retinal ganglion cell; LHON; Leber Hereditary Optic Neuropathy; LGN; lateral geniculate nucleus; V1; primary visual cortex; LPZ; lesion projection zone; CT; cortical thickness; Cortical plasticity; Visual loss; Retinotopic visual areas; Ganglion cell
Optical coherence tomography angiography changes in radial peripapillary capillaries in Leber hereditary optic neuropathy
Keywords: نورروپاتی اپتیکی ارثی Leber; Leber hereditary optic neuropathy; Optical coherence tomography angiography; Optical coherence tomography; Radial peripapillary capillary; Retinal full thickness; Peripapillary retinal nerve fiber layer;
Mitochonic Acid 5 (MA-5) Facilitates ATP Synthase Oligomerization and Cell Survival in Various Mitochondrial Diseases
Keywords: نورروپاتی اپتیکی ارثی Leber; MA-5; 4-(2,4-difluorophenyl)-2-(1H-indole-3-yl)-4-oxobutanoic acid; MELAS; myopathy encephalopathy lactic acidosis and stroke-like episodes; KSS; Kearns-Sayre syndrome; LHON; Leber hereditary optic neuropathy; ETC; electron transfer complex; BSO; l-buthio
Gene Therapy for Leber Hereditary Optic Neuropathy
Keywords: نورروپاتی اپتیکی ارثی Leber; ETDRS; Early Treatment Diabetic Retinopathy Study; GEE; generalized estimating equation; HM; hand movements; LHON; Leber hereditary optic neuropathy; logMAR; logarithm of the minimum angle of resolution; NAb; neutralizing antibody; OCT; optical coherence
Gene Therapy for Leber Hereditary Optic Neuropathy
Keywords: نورروپاتی اپتیکی ارثی Leber; AAV; adeno-associated virus vector; ACF; anterior chamber fluid; DMEM; Dulbecco's modified Eagle's medium; ETDRS; Early Treatment Diabetic Retinopathy Study; IOP; intraocular pressure; LHON; Leber hereditary optic neuropathy; mtDNA; mitochondrial DNA; NAb
Increased expression of ApoE and protection from amyloid-beta toxicity in transmitochondrial cybrids with haplogroup K mtDNA
Keywords: نورروپاتی اپتیکی ارثی Leber; 5-aza-dC; 5-aza-2â²-deoxycytidine; AD; Alzheimer's disease; AMD; Age-related Macular Degeneration; APOE; apolipoprotein E; ARPE-19; retinal pigmented epithelium cell line; ATP; adenosine triphosphate; BSA; bovine serum albumin; DMEM; Dulbecco's modified
A new mutation in MT-ND1 m.3928G>C p.V208L causes Leigh disease with infantile spasms
Keywords: نورروپاتی اپتیکی ارثی Leber; EEG; electroencephalogram; PAGE; polyacrylamide gel electrophoresis; mtDNA; mitochondrial DNA; LHON; Leber hereditary optic neuropathy; MELAS; mitochondrial encephalomyopathy with lactic acidosis and stroke like episodes; HRM; high resolution melt; PCR; p
Mitochondrial disorders: aetiologies, models systems, and candidate therapies
Keywords: نورروپاتی اپتیکی ارثی Leber; mitochondrial disease; gene therapy; Leber hereditary optic neuropathy
LHON/MELAS overlap mutation in ND1 subunit of mitochondrial complex I affects ubiquinone binding as revealed by modeling in Escherichia coli NDH-1
Keywords: نورروپاتی اپتیکی ارثی Leber; d-NADH; deamino-NADH; DB; decylubiquinone; HAR; hexaammineruthenium; LHON; Leber hereditary optic neuropathy; MELAS; mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome; mtDNA; mitochondrial DNA; NDH-1; bacterial prot
Initial experience in the treatment of inherited mitochondrial disease with EPI-743
Keywords: نورروپاتی اپتیکی ارثی Leber; ARE; antioxidant response element; BSO; l-buthionine-(S,R)-sulfoximine; FRDA; Friedreich ataxia; HMPAO; technetium-99m-hexamethylpropyleneamine oxime; KSS; Kearns-Sayre syndrome; LHON; Leber hereditary optic neuropathy; LS; Leigh syndrome; MELAS; Mitoch
Mitochondrial bioenergetics and drug-induced toxicity in a panel of mouse embryonic fibroblasts with mitochondrial DNA single nucleotide polymorphisms
Keywords: نورروپاتی اپتیکی ارثی Leber; ATP; adenosine triphosphate; BSA; bovine serum albumin; 2-DG; 2-deoxy-d-glucose; DMSO; dimethyl sulfoxide; DTNB; 5,5â² dithiobis 2 nitrobenzoic acid; FCCP; Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone; LHON; Leber hereditary optic neuropathy; MEFs;
Leber hereditary optic neuropathy – Therapeutic challenges and early promise
Keywords: نورروپاتی اپتیکی ارثی Leber; gene therapy; idebenone; Leber hereditary optic neuropathy; LHON; mitochondrial DNA; optic atrophy
Atypical presentation of Leigh syndrome associated with a Leber hereditary optic neuropathy primary mitochondrial DNA mutation
Keywords: نورروپاتی اپتیکی ارثی Leber; Atypical Leigh syndrome; Leber hereditary optic neuropathy; Mitochondrial DNA mutation; Phenotypic variation;
Mitochondrial optic neuropathies - Disease mechanisms and therapeutic strategies
Keywords: نورروپاتی اپتیکی ارثی Leber; Dominant optic atrophy; Glaucoma; Hereditary spastic paraplegia; Leber hereditary optic neuropathy; Mitochondrial DNA; Mitofusin; Multiple sclerosis; Neuroprotection; Optic neuritis; Optic neuropathy; Retinal ganglion cell;
Genotype-phenotype correlations in Leber hereditary optic neuropathy
Keywords: نورروپاتی اپتیکی ارثی Leber; Leber hereditary optic neuropathy; Optic nerve; Mitochondrial DNA mutation; Apoptosis; ROS;
Patients with Leber hereditary optic neuropathy fail to compensate impaired oxidative phosphorylation
Keywords: نورروپاتی اپتیکی ارثی Leber; Biochemical phenotype; Leber hereditary optic neuropathy; Mitochondrial density; Oxidative phosphorylation; Peripheral blood mononuclear cell;
Very low penetrance of Leber’s hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation
Keywords: نورروپاتی اپتیکی ارثی Leber; Leber hereditary optic neuropathy; Mitochondrial DNA; Mutation; Visual loss; Penetrance; Haplotype; Modifiers; Chinese; ND1
The Neuro-ophthalmology of Mitochondrial Disease
Keywords: نورروپاتی اپتیکی ارثی Leber; chronic progressive external ophthalmoplegia; dominant optic atrophy; Kearns-Sayre syndrome; Leber hereditary optic neuropathy; MELAS; mitochondria; NARP; neuro-ophthalmology; pigmentary retinopathy
Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis
Keywords: نورروپاتی اپتیکی ارثی Leber; Multiple sclerosis; Leber hereditary optic neuropathy; CSF; Biomarkers; Proteomics
A family with 3460G>A and 11778G>A mutations and haplogroup analysis of Polish Leber hereditary optic neuropathy patients
Keywords: نورروپاتی اپتیکی ارثی Leber; Leber hereditary optic neuropathy; Mitochondrial DNA; Double mutation
You're Too Old for That
Keywords: نورروپاتی اپتیکی ارثی Leber; central scotoma; Leber hereditary optic neuropathy;