MYSTERY CASE: RETINAL PIGMENT EPITHELIAL DYSTROPHY IN A PATIENT WITH POLYNEUROPATHY-Reference-Cited by-同舟云学术

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MYSTERY CASE: RETINAL PIGMENT EPITHELIAL DYSTROPHY IN A PATIENT WITH POLYNEUROPATHY

Published:2021-09 Issue:1 Volume:15 Page:S25-S31
ISSN:1935-1089
Container-title:RETINAL Cases & Brief Reports
language:en
Short-container-title:

Author:

Pimentel Sergio L. G.,Misawa Mariana A. M.,Conci Lívia S.,Takahashi Beatriz S.,Lima Luiz H.,Balaratnasingam Chandrakumar,Agarwal Anita,Cunha de Souza Eduardo

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Ophthalmology,General Medicine

Reference14 articles.

1. ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease;Montecchiani;Brain,2016

2. Charcot-Marie-Tooth disease and other genetic polyneuropathies;Ramchandren;CONTINUUM: Lifelong Learn Neurol,2017

3. Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2;Züchner;Ann Neurol,2006

4. Characterization of Charcot-Marie-Tooth optic neuropathy;Botsford;J Neurol,2017

5. Pupil abnormalities in 131 cases of genetically defined inherited peripheral neuropathy;Houlden;Eye,2008

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