Ophthalmic Manifestations of Danon Disease
Authors:
- Arlene DrackADArlene Drack
- Matthew TaylorMTMatthew Taylor
- Lisa KuLKLisa Ku
- Jeffrey L. OlsonJOJeffrey L. Olson
- Darren GregoryDGDarren Gregory
- Luisa MestroniLMLuisa Mestroni
- Naresh MandavaNMNaresh Mandava
- 1 June 2006
- journal article
- Published by Elsevier in Ophthalmology
- Vol. 113 (6) , 1010-1013
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- CLINICAL FEATURES OF JAPANESE FAMILIES WITH A 402DELT OR A 555–556DELAG MUTATION IN CHOROIDEREMIA GENERetina, 2004
- Charcot–Marie–Tooth features and maculopathy in a patient with Danon diseaseNeurology, 2004
- Clinical findings in a carrier of a new mutation in the choroideremia geneOphthalmology, 2004
- Danon's disease (X-linked vacuolar cardiomyopathy and myopathy): a case with a novel Lamp-2 gene mutationNeuromuscular Disorders, 2002
- Clinicopathological features of genetically confirmed Danon diseaseNeurology, 2002
- Accumulation of autophagic vacuoles and cardiomyopathy in LAMP-2-deficient miceNature, 2000
- Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)Nature, 2000
- Unusual macular findings in a known choroideremia carrierEye, 1998
- Lysosomal glycogen storage disease with normal acid maltaseNeurology, 1981
- ChoroideremiaArchives of Ophthalmology (1950), 1966