OphthalmoplegiaOphthalmoplegia, Chronic Progressive ExternalKearns-Sayre SyndromeBlepharoptosisGenes, DominantMultiple SclerosisDNA, MitochondrialMiller Fisher SyndromePolycystic Kidney, Autosomal DominantOxymetholoneCarcinogenicity TestsPedigreeMitochondria, MuscleKidney TubulesOcular Motility DisordersChronic DiseaseRats, Inbred F344Disease ProgressionAnisocoriaPoint MutationMagnetic Resonance ImagingKidney DiseasesCavernous SinusHerpes Zoster OphthalmicusExophthalmosMutationOculomotor MusclesKidney NeoplasmsKidneyTolosa-Hunt SyndromeDisease Models, AnimalDiplopiaSyndromeOculomotor Nerve DiseasesMitochondrial MyopathiesProteinuriaGenetic LinkageBrainAdenomaDNA Mutational AnalysisMutation, MissenseMitochondrial DiseasesAtaxiaMitochondrial EncephalomyopathiesTRPP Cation ChannelsLod ScoreWernicke EncephalopathyAdenine Nucleotide Translocator 1Abducens NerveCerebellar AtaxiaMuscular DiseasesPhenotypeRetinitis PigmentosaAbducens Nerve DiseasesMultiple Sclerosis, Chronic ProgressiveCranial Nerve DiseasesNystagmus, PathologicOculomotor NerveNeuromuscular DiseasesElectrooculographyAge of OnsetOptic Atrophy, Autosomal DominantMolecular Sequence DataDiffuse Cerebral Sclerosis of SchilderOrbital NeoplasmsOrbital PseudotumorIntestinal Pseudo-ObstructionFacial ParalysisChromosome MappingEye MovementsOrbitGangliosidesPonsBase SequenceTrochlear Nerve DiseasesFatal OutcomePolycystic Kidney DiseasesMyelitis, TransverseDNA-Directed DNA PolymeraseOrbital DiseasesCataractCADASILGuillain-Barre SyndromeParanasal Sinus DiseasesHaplotypesHeterozygotePrednisoloneSpinocerebellar DegenerationsGenes, RecessiveMuscular Atrophy