Occult macular dystrophy with bilateral chronic subfoveal serous retinal detachment associated with a novel RP1L1 mutation (p.S1199P)

Diagnostic Fundus Autofluorescence Patterns in Achromatopsia

(2013) Abigail T. Fahim et al.   AMERICAN JOURNAL OF OPHTHALMOLOGY

Elderly case of pseudo-unilateral occult macular dystrophy with Arg45Trp mutation in RP1L1 gene

(2013) Takashi Okuno et al.   DOCUMENTA OPHTHALMOLOGICA

Autosomal Dominant Occult Macular Dystrophy with an RP1L1 Mutation (R45W)

(2012) Takaaki Hayashi et al.   OPTOMETRY AND VISION SCIENCE

CLINICAL CHARACTERISTICS OF OCCULT MACULAR DYSTROPHY IN FAMILY WITH MUTATION OF RP1L1 GENE

(2012) Kazushige Tsunoda et al.   RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES

FOVEAL CAVITATION AS AN OPTICAL COHERENCE TOMOGRAPHY FINDING IN CENTRAL CONE DYSFUNCTION

(2012) Theodore Leng et al.   RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES

Fundus Autofluorescence in Autosomal Dominant Occult Macular Dystrophy

(2011) Kaoru Fujinami   ARCHIVES OF OPHTHALMOLOGY

ISCEV standard for clinical electro-oculography (2010 update)

(2011) Michael F. Marmor et al.   DOCUMENTA OPHTHALMOLOGICA

ISCEV standard for clinical multifocal electroretinography (mfERG) (2011 edition)

(2011) Donald C. Hood et al.   DOCUMENTA OPHTHALMOLOGICA

Analysis of spectral domain optical coherence tomography findings in occult macular dystrophy

(2010) Young-Gyun Kim et al.   ACTA OPHTHALMOLOGICA

Dominant Mutations in RP1L1 Are Responsible for Occult Macular Dystrophy

(2010) Masakazu Akahori et al.   AMERICAN JOURNAL OF HUMAN GENETICS

ISCEV Standard for full-field clinical electroretinography (2008 update)

(2008) M. F. Marmor et al.   DOCUMENTA OPHTHALMOLOGICA