Cargando…

Analysis of Genetic Mutations in a Cohort of Hereditary Optic Neuropathy in Shanghai, China

PURPOSE: To evaluate the clinical classification and characteristics of hereditary optic neuropathy patients in a single center in China. METHOD: Retrospective case study. Patients diagnosed with hereditary optic neuropathy between January 2014 and December 2015 in the neuro-ophthalmology division i...

Descripción completa

Detalles Bibliográficos
Autores principales:	Gan, Dekang, Li, Mengwei, Wu, Jihong, Sun, Xinghuai, Tian, Guohong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2017
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5733633/ https://www.ncbi.nlm.nih.gov/pubmed/29348930 http://dx.doi.org/10.1155/2017/6186052

Ejemplares similares

Mutations for Leber hereditary optic neuropathy in patients with alcohol and tobacco optic neuropathy
por: Amaral-Fernandes, Marcela Scabello, et al.
Publicado: (2011)

Evaluation of Retinal Nerve Fiber Layer and Ganglion Cell Complex in Patients with Optic Neuritis or Neuromyelitis Optica Spectrum Disorders Using Optical Coherence Tomography in a Chinese Cohort
por: Tian, Guohong, et al.
Publicado: (2015)

Genetic Spectrum and Characteristics of Hereditary Optic Neuropathy in Taiwan
por: Lin, Chao-Wen, et al.
Publicado: (2021)

Identification of novel mitochondrial mutations in Leber’s hereditary optic neuropathy
por: Kumar, Manoj, et al.
Publicado: (2010)

Leber's hereditary optic neuropathy with 3460 mitochondrial DNA mutation.
por: Hwang, Jeong-Min, et al.
Publicado: (2002)

The epidemiology and mutation types of Leber’s hereditary optic neuropathy in Thailand
por: Sathianvichitr, Kanchalika, et al.
Publicado: (2022)

Mitochondrial genetics and therapeutic overview of Leber's hereditary optic neuropathy
por: Manickam, Agaath Hedina, et al.
Publicado: (2017)

Medical Management of Hereditary Optic Neuropathies
por: La Morgia, Chiara, et al.
Publicado: (2014)

Therapeutic Options in Hereditary Optic Neuropathies
por: Amore, Giulia, et al.
Publicado: (2020)

Vitamin B12 in Leber hereditary optic neuropathy mutation carriers: a prospective cohort study
por: Zibold, Julia, et al.
Publicado: (2022)

Current and Future Landscape in Genetic Therapies for Leber Hereditary Optic Neuropathy
por: Shamsnajafabadi, Hoda, et al.
Publicado: (2023)

The Progress of Gene Therapy for Leber's Optic Hereditary Neuropathy
por: Zhang, Yong, et al.
Publicado: (2018)

Mutation Screening of mtDNA Combined Targeted Exon Sequencing in a Cohort With Suspected Hereditary Optic Neuropathy
por: Li, Jian-Kang, et al.
Publicado: (2020)

Point mutations associated with Leber hereditary optic neuropathy in a Latvian population
por: Aitullina, Aleksandra, et al.
Publicado: (2013)

A Rare ND5 Mutation Causing Leber’s Hereditary Optic Neuropathy
por: Pandya, Bhadra U., et al.
Publicado: (2023)

Causes and 3-year-incidence of blindness in Jing-An District, Shanghai, China 2001-2009
por: Wu, Liangcheng, et al.
Publicado: (2011)

Familial aggregation of primary open angle glaucoma in Shanghai, China
por: Kong, Xiangmei, et al.
Publicado: (2013)

Genetic spectrum in a cohort of patients with distal hereditary motor neuropathy
por: Wu, Chengsi, et al.
Publicado: (2022)

Leber hereditary optic neuropathy: current perspectives
por: Meyerson, Cherise, et al.
Publicado: (2015)

Leber’s hereditary optic neuropathy - Case report
por: Iorga, Raluca Eugenia, et al.
Publicado: (2018)

Leber’s Hereditary Optic Neuropathy – Case Discussion
por: Culea, Cristina, et al.
Publicado: (2019)

Arterial sheathing in Leber hereditary optic neuropathy
por: Zhou, Henry W., et al.
Publicado: (2022)

Clinical Overview of Leber Hereditary Optic Neuropathy
por: Stramkauskaitė, Almina, et al.
Publicado: (2022)

Leber’s Hereditary Optic Neuropathy and Hypertrophic Cardiomyopathy
por: Hey, Thomas Morris, et al.
Publicado: (2022)

Developments in the Treatment of Leber Hereditary Optic Neuropathy
por: Chen, Benson S., et al.
Publicado: (2022)

Traumatic Cataract in Children in Eastern China: Shanghai Pediatric Cataract Study
por: Du, Yu, et al.
Publicado: (2018)

Mutation survey of the optic atrophy 1 gene in 193 Chinese families with suspected hereditary optic neuropathy
por: Chen, Yabin, et al.
Publicado: (2013)

Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutations
por: Pfeffer, Gerald, et al.
Publicado: (2013)

Frequency of primary mutations of Leber's hereditary optic neuropathy patients in North Indian population
por: Mishra, Anushree, et al.
Publicado: (2017)

Leber’s hereditary optic neuropathy: course of disease in consideration of idebenone treatment and type of mutation
por: Tonagel, Felix, et al.
Publicado: (2020)

Leber’s hereditary optic neuropathy companied with multiple-related diseases
por: Sun, Ming-ming, et al.
Publicado: (2022)

Leber’s Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited
por: Abu-Amero, Khaled K.
Publicado: (2011)

Gene–environment interactions in Leber hereditary optic neuropathy
por: Kirkman, Matthew Anthony, et al.
Publicado: (2009)

Leber’s hereditary optic neuropathy is multiorgan not mono-organ
por: Finsterer, Josef, et al.
Publicado: (2016)

Leber hereditary optic neuropathy: bridging the translational gap
por: Jurkute, Neringa, et al.
Publicado: (2017)

Leber’s Hereditary Optic Neuropathy – Reply Letter to the Editor
por: Manole, Cristina, et al.
Publicado: (2020)

Gene Therapies for the Treatment of Leber Hereditary Optic Neuropathy
por: Sahel, José-Alain, et al.
Publicado: (2021)

Editorial: Hereditary Optic Neuropathies: A New Perspective
por: Carelli, Valerio, et al.
Publicado: (2021)

Leber Hereditary Optic Neuropathy: Review of Treatment and Management
por: Hage, Rabih, et al.
Publicado: (2021)

Mitochondrial Genetic Heterogeneity in Leber’s Hereditary Optic Neuropathy: Original Study with Meta-Analysis
por: Jha, Rajan Kumar, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_jvan9cs27h7tgkm9k2t73tvaja