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Multimodal investigation of melanopsin retinal ganglion cells in Alzheimer's disease
Download from doi.orgChromatic Pupillometry in Isolated Rapid Eye Movement Sleep Behavior Disorder
Download from onlinelibrary.wiley.comImpaired complex I repair causes recessive Leber’s hereditary optic neuropathy
Download from doi.orgMitochondrial diseases in adults
UploadMutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy
Download from doi.orgFunctional MRI study in a case of Charles Bonnet syndrome related to LHON
Download from doi.orgMutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder
Download from www.nature.comSyndromic parkinsonism and dementia associated with OPA1 missense mutations
Download from onlinelibrary.wiley.comDiffusion Tensor Imaging Mapping of Brain White Matter Pathology in Mitochondrial Optic Neuropathies
Download from www.ajnr.orgOPA1-related auditory neuropathy: Site of lesion and outcome of cochlear implantation
Download from doi.orgEarly Macular Retinal Ganglion Cell Loss in Dominant Optic Atrophy: Genotype-Phenotype Correlation
Upload'Behr syndrome' with OPA1 compound heterozygote mutations
Download from doi.orgMedical Management of Hereditary Optic Neuropathies
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