Keywords: سندرم Kearns-Sayre; 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
مقالات ISI سندرم Kearns-Sayre (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.
Keywords: سندرم Kearns-Sayre; CNS; central nervous system; NARP; Neuropathy Ataxia Retinitis Pigmentosa; KSS; Kearns-Sayre Syndrome; MILS; Maternally Inherited Leigh Syndrome; AMD; Age-related Macular Degeneration; MIDD; Mitochondrial Syndrome of Maternally Inherited Diabetes and Deaf
Keywords: سندرم Kearns-Sayre; AHS; Alpers-Huttenlocher Syndrome; EPC; epilepsia-partialis-continua; KSS; Kearns-Sayre Syndrome; MELAS; Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-like episodes; MIDD; Maternally Inherited Diabetes and Deafness; mtDNA; Mitochondrial DNA;
Keywords: سندرم Kearns-Sayre; Mitochondrial diseases; MtDNA; Nuclear genome; Progressive external ophthalmoplegia; Exercise intolerance; Cerebellar ataxia; Refractory epilepsy; Movement disorders; Maladies mitochondriales; ADNmt; Génome nucléaire; Ophtalmoplégie progressive externe
Mitochonic Acid 5 (MA-5) Facilitates ATP Synthase Oligomerization and Cell Survival in Various Mitochondrial Diseases
Keywords: سندرم Kearns-Sayre; 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
The Neuro-ophthalmology of Mitochondrial Disease
Keywords: سندرم Kearns-Sayre; chronic progressive external ophthalmoplegia; dominant optic atrophy; Kearns-Sayre syndrome; Leber hereditary optic neuropathy; MELAS; mitochondria; NARP; neuro-ophthalmology; pigmentary retinopathy
Kearns-Sayre syndrome: electro-vectorcardiographic evolution for left septal fascicular block of the his bundle
Keywords: سندرم Kearns-Sayre; Kearns-Sayre syndrome; Prominent anterior forces; Fascicular blocks; Left septal fascicular block; Trifascicular block
Coinheritance of long QT syndrome and Kearns-Sayre syndrome
Keywords: سندرم Kearns-Sayre; Kearns-Sayre syndrome; Mitochondrial disorder; Long QT syndrome mutation; Torsades de pointes; Complete atrioventricular block;
Afección cardÃaca en el sÃndrome de Kearns-Sayre
Keywords: سندرم Kearns-Sayre; SÃndrome de Kearns-Sayre; ElectrocardiografÃa; ElectrofisiologÃa; Estudios de seguimiento; Kearns-Sayre syndrome; Electrocardiography; Electrophysiology; Follow-up studies;
Cardiac Involvement in Kearns-Sayre Syndrome
Keywords: سندرم Kearns-Sayre; Kearns-Sayre syndrome; Electrocardiography; Electrophysiology; Follow-up studies; SÃndrome de Kearns-Sayre; ElectrocardiografÃa; ElectrofisiologÃa; Estudios de seguimiento;
Common and cell type-specific responses of human cells to mitochondrial dysfunction
Keywords: سندرم Kearns-Sayre; Ï0; Mitochondrial DNA; Mitochondrial dysfunction; Kearns-Sayre syndrome; Aging;