Cargando…

High-Resolution En Face Images of Microcystic Macular Edema in Patients with Autosomal Dominant Optic Atrophy

The purpose of this study was to investigate the characteristics of microcystic macular edema (MME) determined from the en face images obtained by an adaptive optics (AO) fundus camera in patients with autosomal dominant optic atrophy (ADOA) and to try to determine the mechanisms underlying the dege...

Descripción completa

Detalles Bibliográficos
Autores principales:	Gocho, Kiyoko, Kikuchi, Sachiko, Kabuto, Takenori, Kameya, Shuhei, Shinoda, Kei, Mizota, Atsushi, Yamaki, Kunihiko, Takahashi, Hiroshi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi Publishing Corporation 2013
Materias:	Clinical Study
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3863472/ https://www.ncbi.nlm.nih.gov/pubmed/24369534 http://dx.doi.org/10.1155/2013/676803

Ejemplares similares

Detailed analysis of family with autosomal recessive bestrophinopathy associated with new BEST1 mutation
por: Kubota, Daiki, et al.
Publicado: (2016)

High-Resolution Imaging of Patients with Bietti Crystalline Dystrophy with CYP4V2 Mutation
por: Gocho, Kiyoko, et al.
Publicado: (2014)

A new mutation in the RP1L1 gene in a patient with occult macular dystrophy associated with a depolarizing pattern of focal macular electroretinograms
por: Kabuto, Takenori, et al.
Publicado: (2012)

Detailed Morphological Changes of Foveoschisis in Patient with X-Linked Retinoschisis Detected by SD-OCT and Adaptive Optics Fundus Camera
por: Akeo, Keiichiro, et al.
Publicado: (2015)

Multimodal imaging of a case of peripheral cone dystrophy
por: Ito, Naoko, et al.
Publicado: (2015)

Cone Dystrophy in Patient with Homozygous RP1L1 Mutation
por: Kikuchi, Sachiko, et al.
Publicado: (2015)

MACULAR ATROPHY AND PHENOTYPIC VARIABILITY IN AUTOSOMAL DOMINANT STARGARDT-LIKE MACULAR DYSTROPHY DUE TO PROM1 MUTATION
por: Ricca, Aaron M., et al.
Publicado: (2023)

Optic Neuritis Is Associated with Inner Nuclear Layer Thickening and Microcystic Macular Edema Independently of Multiple Sclerosis
por: Kaufhold, Falko, et al.
Publicado: (2013)

Inhibition of Hedgehog signaling suppresses proliferation and microcyst formation of human Autosomal Dominant Polycystic Kidney Disease cells
por: Silva, Luciane M., et al.
Publicado: (2018)

Visual function and disability are associated with microcystic macular edema, macular and peripapillary vessel density in patients with neuromyelitis optica spectrum disorder
por: Li, Jin, et al.
Publicado: (2022)

Autosomal dominant optic atrophy with OPA1 gene mutations accompanied by auditory neuropathy and other systemic complications in a Japanese cohort
por: Maeda-Katahira, Akiko, et al.
Publicado: (2019)

Correction: Optic Neuritis Is Associated with Inner Nuclear Layer Thickening and Microcystic Macular Edema Independently of Multiple Sclerosis
por: Kaufhold, Falko, et al.
Publicado: (2013)

New observation of microcystic macular edema as a mild form of cystoid macular lesions after standard phacoemulsification: Prevalence and risk factors
por: Yoon, Dong H., et al.
Publicado: (2018)

Genetic defects of CHM and visual acuity outcome in 24 choroideremia patients from 16 Japanese families
por: Hayashi, Takaaki, et al.
Publicado: (2020)

Mitochondrial oxidative phosphorylation in autosomal dominant optic atrophy
por: Mayorov, Vladimir I, et al.
Publicado: (2008)

Assessment of Macular Function during Vitrectomy: New Approach Using Intraoperative Focal Macular Electroretinograms
por: Matsumoto, Celso Soiti, et al.
Publicado: (2015)

Transient Increase and Delay of Multifocal Electroretinograms Following Laser Photocoagulations for Diabetic Macular Edema
por: Shimada, Yoshiaki, et al.
Publicado: (2021)

Cystoid Macular Edema: Possible Complication of Infliximab Therapy in Behçet's Disease
por: Ikewaki, Junko, et al.
Publicado: (2010)

Visual and psychological morbidity among patients with autosomal dominant optic atrophy
por: Bailie, Maura, et al.
Publicado: (2013)

Atrophy of the central neuroretina in patients treated for diabetic macular edema
por: Karst, Sonja G., et al.
Publicado: (2019)

Macular Microcysts in Mitochondrial Optic Neuropathies: Prevalence and Retinal Layer Thickness Measurements
por: Carbonelli, Michele, et al.
Publicado: (2015)

Genomic deletions in OPA1 in Danish patients with autosomal dominant optic atrophy
por: Almind, Gitte J, et al.
Publicado: (2011)

Autosomal dominant optic atrophy and cataract “plus” phenotype including axonal neuropathy
por: Horga, Alejandro, et al.
Publicado: (2019)

Microcystic adenoma of the pancreas.
por: Heatley, M. K., et al.
Publicado: (1991)

Cyst infection in autosomal dominant polycystic kidney disease: penetration of meropenem into infected cysts
por: Hamanoue, Satoshi, et al.
Publicado: (2018)

Comparison of Lamina Cribrosa Morphology in Normal Tension Glaucoma and Autosomal-Dominant Optic Atrophy
por: Kim, Gyu-Nam, et al.
Publicado: (2020)

Inhibition of autophagy curtails visual loss in a model of autosomal dominant optic atrophy
por: Zaninello, Marta, et al.
Publicado: (2020)

Comparing cortical signatures of atrophy between late-onset and autosomal dominant Alzheimer disease
por: Dincer, Aylin, et al.
Publicado: (2020)

Vision‐related quality of life and visual ability in patients with autosomal dominant optic atrophy
por: Eckmann‐Hansen, Christina, et al.
Publicado: (2022)

Microcystic Changes in the Retinal Internal Nuclear Layer Associated with Optic Atrophy: A Prospective Study
por: Wolff, Benjamin, et al.
Publicado: (2014)

Arginine-Restricted Therapy Resistant Bilateral Macular Edema Associated with Gyrate Atrophy
por: Doguizi, Sibel, et al.
Publicado: (2015)

A Korean Family with an Early-Onset Autosomal Dominant Macular Dystrophy Resembling North Carolina Macular Dystrophy
por: Kim, Sang Jin, et al.
Publicado: (2006)

Electroretinographic Assessments of Macular Function after Brilliant Blue G Staining for Inner Limiting Membrane Peeling
por: Terauchi, Gaku, et al.
Publicado: (2022)

Pars Plana Vitrectomy Combined with Focal Endolaser Photocoagulation for Idiopathic Macular Telangiectasia
por: Terauchi, Gaku, et al.
Publicado: (2014)

Identification of two novel OPA1 mutations in Chinese families with autosomal dominant optic atrophy
por: Li, Yang, et al.
Publicado: (2008)

Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophy
por: Gallus, Gian Nicola, et al.
Publicado: (2010)

Sustained intracellular calcium rise mediates neuronal mitophagy in models of autosomal dominant optic atrophy
por: Zaninello, Marta, et al.
Publicado: (2021)

Visual Function and Inner Retinal Structure in Relation to Birth Factors in Autosomal Dominant Optic Atrophy
por: Eckmann-Hansen, Christina, et al.
Publicado: (2023)

Microcystic Variant of Urothelial Carcinoma
por: Venyo, Anthony Kodzo-Grey
Publicado: (2013)

Lithium-Associated Kidney Microcysts
por: Tuazon, Jennifer, et al.
Publicado: (2008)

Cannot write session to /tmp/vufind_sessions/sess_09tdhq5pnq624fuqctf0n7cpo6