An 18-year-old man with dominant optic atrophy (DOA). The fundus
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A multiple sclerosis‐like disorder in patients with OPA1 mutations
Colour fundus and OCT findings in DOA. The images were obtained
2020–2021 BCSC Basic and Clinical Science Course™
CIMB, Free Full-Text
Autosomal Dominant Optic Atrophy - ScienceDirect
Dominant Optic Atrophy: A Teenager with Progressive Painless
Inherited dominant optic neuropathy: from clinical studies to gene
Therapeutic Options in Hereditary Optic Neuropathies
Young patient with long-standing reduced vision
2020–2021 BCSC Basic and Clinical Science Course™
That's Egg on Your Face
Hereditary Optic Neuropathies
Frontiers Medical Management of Hereditary Optic Neuropathies
Comparison of the clinical and genetic features of autosomal
Fundus manifestations of patients with DOA and LHON. (A-F) LHON-A
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