Ophthalmic manifestations of inherited neurodegenerative disorders. - Wikidata - awgldk - TriplyDB

Ophthalmic manifestations of inherited neurodegenerative disorders.

Ophthalmic manifestations of inherited neurodegenerative disorders.

http://www.wikidata.org/entity/Q38212813

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Neurodegeneration severity can be predicted from early microglia alterations monitored in vivo in a mouse model of chronic glaucoma.In vivo dynamics of retinal microglial activation during neurodegeneration: confocal ophthalmoscopic imaging and cell morphometry in mouse glaucoma Rescue of Glaucomatous Neurodegeneration by Differentially Modulating Neuronal Endoplasmic Reticulum Stress Molecules.The New Zealand Neuromuscular Disease Patient Registry; Five Years and a Thousand Patients.Ocular and neurodevelopmental features of Duchenne muscular dystrophy: a signature of dystrophin function in the central nervous system.Optical coherence tomography findings in Huntington's disease: a potential biomarker of disease progression.Spectropathology-corroborated multimodal quantitative imaging biomarkers for neuroretinal degeneration in diabetic retinopathy.Vision Loss in a Teenage Girl With Postconcussion Syndrome.An Assessment of Retinal Nerve Fiber Layer Thickness in Non-Diabetic Obese Children and Adolescents.Acute vitreoretinal trauma and inflammation after traumatic brain injury in mice.Reduced retinal nerve fibre layer thickness in children with severe obesity

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Ophthalmic manifestations of inherited neurodegenerative disorders.

http://www.wikidata.org/entity/Q38212813

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Ophthalmic manifestations of inherited neurodegenerative disorders.

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Ophthalmic manifestations of inherited neurodegenerative disorders.

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Ophthalmic manifestations of inherited neurodegenerative disorders.

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NRNEUROL.2014.79

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Nature Reviews Neurology

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Ophthalmic manifestations of inherited neurodegenerative disorders.

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Helen V Danesh-Meyer

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Richard H Roxburgh

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Neurodegeneration with brain iron accumulation

Diagnosis, natural history, and management of Charcot–Marie–Tooth disease

A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9

Mitochondrial dysfunction as a cause of optic neuropathies

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nrneurol.2014.79

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349-362

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scholarly article

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10.1038/NRNEUROL.2014.79

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Hannah M Kersten

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2014-05-20T00:00:00Z

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262538804

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neurodegeneration