A Proposal for Classification of Retinal Degeneration in Spinocerebellar Ataxia Type 7

Ophthalmological and Neurologic Manifestations in Pre-clinical and Clinical Phases of Spinocerebellar Ataxia Type 7

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Ophthalmological changes in hereditary spastic paraplegia and other genetic diseases with spastic paraplegia

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Optical coherence tomography in multiple sclerosis

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Clinical, ophthalmological, imaging and genetic features in Brazilian patients with ARSACS Characterization of ARSACS phenotype in Brazil

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Antisense oligonucleotides targeting mutant Ataxin-7 restore visual function in a mouse model of spinocerebellar ataxia type 7

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Ophthalmic features of spinocerebellar ataxia type 7

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Optical Coherence Tomography in Alzheimer’s Disease and Other Neurodegenerative Diseases

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Ataxia Severity Correlates with White Matter Degeneration in Spinocerebellar Ataxia Type 7

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Phenotype variability and early onset ataxia symptoms in spinocerebellar ataxia type 7: comparison and correlation with other spinocerebellar ataxias

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Specific cerebellar and cortical degeneration correlates with ataxia severity in spinocerebellar ataxia type 7

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Spinocerebellar Ataxia Type 7: A Neurodegenerative Disorder with Peripheral Neuropathy

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Ophthalmic manifestations of inherited neurodegenerative disorders

(2014) Hannah M. Kersten et al.   Nature Reviews Neurology

A comprehensive clinical and genetic study of a large Mexican population with spinocerebellar ataxia type 7

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Proposed Lexicon for Anatomic Landmarks in Normal Posterior Segment Spectral-Domain Optical Coherence Tomography

(2014) Giovanni Staurenghi et al.   OPHTHALMOLOGY

RNA Interference-Based Therapy for Spinocerebellar Ataxia Type 7 Retinal Degeneration

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Causes and consequences of inherited cone disorders

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Optical coherence tomography findings in spinocerebellar ataxia-3

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Spinocerebellar Ataxia Type 7: Clinical Course, Phenotype–Genotype Correlations, and Neuropathology

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Clinical Course, Genetic Etiology, and Visual Outcome in Cone and Cone–Rod Dystrophy

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Neuro-Ophthalmologic Features of Spinocerebellar Ataxia Type 7

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Two Patients With Spinocerebellar Ataxia Type 7 Presenting With Profound Binocular Visual Loss Yet Minimal Ophthalmoscopic Findings

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Ophthalmic Features of Spinocerebellar Ataxia Type 7

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Macular Dysfunction and Morphology in Spinocerebellar Ataxia Type 7 (SCA 7)

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Visual system involvement in patients with Friedreich's ataxia

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