Related references
Note: Only part of the references are listed.Idebenone: When an antioxidant is not an antioxidant
Nuri Gueven et al.
REDOX BIOLOGY (2021)
Characteristics of Japanese patients with Leber's hereditary optic neuropathy and idebenone trial: a prospective, interventional, non-comparative study
Hiroto Ishikawa et al.
JAPANESE JOURNAL OF OPHTHALMOLOGY (2021)
Clinical Features of Chinese Sporadic Leber Hereditary Optic Neuropathy Caused by Rare Primary mtDNA Mutations
Shilei Cui et al.
JOURNAL OF NEURO-OPHTHALMOLOGY (2020)
Demographics of a Large International Population of Patients Affected by Leber's Hereditary Optic Neuropathy
Lissa Poincenot et al.
OPHTHALMOLOGY (2020)
Imaging Methods for Differentiating Pediatric Papilledema from Pseudopapilledema A Report by the American Academy of Ophthalmology
Melinda Y. Chang et al.
OPHTHALMOLOGY (2020)
Genotypic and phenotypic characteristics of Korean children with childhood-onset Leber's hereditary optic neuropathy
Ye Jin Ahn et al.
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY (2020)
Mitochondrial genome variation in male LHON patients with the m.11778G > A mutation
Agnieszka Piotrowska-Nowak et al.
METABOLIC BRAIN DISEASE (2020)
Real-World Clinical Experience With Idebenone in the Treatment of Leber Hereditary Optic Neuropathy
Claudia B. Catarino et al.
JOURNAL OF NEURO-OPHTHALMOLOGY (2020)
Leber Hereditary Optic Neuropathy: Case Report and Literature Review
Asia Filatov et al.
CUREUS JOURNAL OF MEDICAL SCIENCE (2020)
Raxone in the Leber optical neuropathy: Parisian experience
C. Orssaud et al.
JOURNAL FRANCAIS D OPHTALMOLOGIE (2019)
Charles Bonnet syndrome in Leber's hereditary optic neuropathy
Hana Kolarova et al.
JOURNAL OF NEUROLOGY (2019)
Analysis of Inherited Optic Neuropathies
Simona Lazdinyte et al.
KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE (2019)
What are the characteristics and progression of visual field defects in patients with Leber hereditary optic neuropathy: a prospective single-centre study in China
Hong-Li Liu et al.
BMJ OPEN (2019)
Immune Response and Intraocular Inflammation in Patients With Leber Hereditary Optic Neuropathy Treated With Intravitreal Injection of Recombinant Adeno-Associated Virus 2 Carrying the ND4 Gene A Secondary Analysis of a Phase 1/2 Clinical Trial
Celine Bouquet et al.
JAMA OPHTHALMOLOGY (2019)
Prognostic factors for visual acuity in patients with Leber's hereditary optic neuropathy after rAAV2-ND4 gene therapy
Yong Zhang et al.
CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY (2019)
Unilateral cone-rod dysfunction and retinal thinning in a child carrying the 14484 mutation of Leber hereditary optic neuropathy
Ahmed Kassem et al.
JOURNAL OF AAPOS (2019)
Mitochondrial m.13513G>A Point Mutation in ND5 in a 16-Year-Old Man with Leber Hereditary Optic Neuropathy Detected by Next-Generation Sequencing
Daniel Vazquez-Justes et al.
JOURNAL OF PEDIATRIC GENETICS (2019)
Leber's hereditary optic neuropathy caused by a mutation in mitochondrial tRNAThr in eight Chinese pedigrees
Juanjuan Zhang et al.
MITOCHONDRION (2018)
Hereditary optic neuropathies in pediatric ophthalmology
C. Orssaud et al.
JOURNAL FRANCAIS D OPHTALMOLOGIE (2018)
Cardiac Disorders in Patients With Leber Hereditary Optic Neuropathy
Christophe Orssaud
JOURNAL OF NEURO-OPHTHALMOLOGY (2018)
MRI of the Optic Nerves and Chiasm in Patients With Leber Hereditary Optic Neuropathy
Christelle Blanc et al.
JOURNAL OF NEURO-OPHTHALMOLOGY (2018)
MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load
Yi Shiau Ng et al.
EBIOMEDICINE (2018)
Visual Field Variability after Gene Therapy for Leber's Hereditary Optic Neuropathy
Jia-jia Yuan et al.
OPHTHALMIC RESEARCH (2018)
Mitochondrial genetics and therapeutic overview of Leber's hereditary optic neuropathy
Agaath Hedina Manickam et al.
INDIAN JOURNAL OF OPHTHALMOLOGY (2017)
Characterization of a Leber's hereditary optic neuropathy (LHON) family harboring two primary LHON mutations m.11778G > A and m.14484T > C of the mitochondrial DNA
Claudia B. Catarino et al.
MITOCHONDRION (2017)
Pediatric Optic Neuritis
Melinda Y. Chang et al.
SEMINARS IN PEDIATRIC NEUROLOGY (2017)
Genetic and Clinical Analyses of DOA and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic Neuropathy
Yadi Li et al.
PLOS ONE (2017)
Childhood-onset Leber hereditary optic neuropathy
Anna Majander et al.
BRITISH JOURNAL OF OPHTHALMOLOGY (2017)
Profound vision loss impairs psychological well-being in young and middle-aged individuals
Giancarlo A. Garcia et al.
CLINICAL OPHTHALMOLOGY (2017)
A neurodegenerative perspective on mitochondrial optic neuropathies
Patrick Yu-Wai-Man et al.
ACTA NEUROPATHOLOGICA (2016)
Idebenone: A Review in Leber's Hereditary Optic Neuropathy
Katherine A. Lyseng-Williamson
DRUGS (2016)
Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation
Pingping Jiang et al.
HUMAN MOLECULAR GENETICS (2016)
Optic disc drusen in children: Advantages of various imaging modalities
S. Naoum et al.
JOURNAL FRANCAIS D OPHTALMOLOGIE (2016)
Evaluation of Leber's hereditary optic neuropathy patients prior to a gene therapy clinical trial
Shuo Yang et al.
MEDICINE (2016)
Long-term outcomes of gene therapy for the treatment of Leber's hereditary optic neuropathy
Shuo Yang et al.
EBIOMEDICINE (2016)
Changes in Choroidal Thickness follow the RNFL Changes in Leber's Hereditary Optic Neuropathy
Enrico Borrelli et al.
SCIENTIFIC REPORTS (2016)
Mitochondrial ND1 Variants in 1281 Chinese Subjects With Leber's Hereditary Optic Neuropathy
Yanchun Ji et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2016)
Leber hereditary optic neuropathy: current perspectives
Cherise Meyerson et al.
CLINICAL OPHTHALMOLOGY (2015)
Leber hereditary optic neuropathy mutations and toxic-genetic optic neuropathy - Authors' response
Marko Kervinen et al.
ACTA OPHTHALMOLOGICA (2014)
Pathogenic Mitochondrial DNA Mutations and Associated Clinical Features in Korean Patients With Leber's Hereditary Optic Neuropathy
Hae Ri Yum et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2014)
Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese families
Yanchun Ji et al.
JOURNAL OF HUMAN GENETICS (2014)
Leber's hereditary optic neuropathy caused by the homoplasmic ND1 m.3635G > A mutation in nine Han Chinese families
Juanjuan Zhang et al.
MITOCHONDRION (2014)
Medical management of hereditary optic neuropathies
Chiara La Morgia et al.
FRONTIERS IN NEUROLOGY (2014)
Prevalence of the primary LHON mutations in Northern Finland associated with bilateral optic atrophy and tobacco-alcohol amblyopia
Paula Korkiamaki et al.
ACTA OPHTHALMOLOGICA (2013)
Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutations
Gerald Pfeffer et al.
NEUROLOGY (2013)
Vision improvement in a Taiwanese (Han Chinese) family with Leber's hereditary optic neuropathy
Hong-Zin Lin et al.
KAOHSIUNG JOURNAL OF MEDICAL SCIENCES (2012)
Leber's Hereditary Optic Neuropathy Is Associated with the T3866C Mutation in Mitochondrial ND1 Gene in Three Han Chinese Families
Xiangtian Zhou et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2012)
Central retinal vein occlusion as the initial manifestation of LHON/MELAS overlap syndrome with mitochondrial DNA G13513A mutation-Case report and literature review
Yi-Ting Hsieh et al.
OPHTHALMIC GENETICS (2011)
Leber's Hereditary Optic Neuropathy Is Associated with the T12338C Mutation in Mitochondrial ND5 Gene in Six Han Chinese Families
Xiao-Ling Liu et al.
OPHTHALMOLOGY (2011)
Leber's Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited
Khaled K. Abu-Amero
MIDDLE EAST AFRICAN JOURNAL OF OPHTHALMOLOGY (2011)
mtDNA m.3635G>A may be classified as a common primary mutation for Leber hereditary optic neuropathy in the Chinese population
Xiaoyun Jia et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2010)
Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families
Juanjuan Zhang et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2010)
Ophthalmological findings in children and young adults with genetically verified mitochondrial disease
M. A. Gronlund et al.
BRITISH JOURNAL OF OPHTHALMOLOGY (2010)
Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation
Xiangtian Zhou et al.
MOLECULAR GENETICS AND METABOLISM (2010)
Leber's Hereditary Optic Neuropathy Affects Only Female Matrilineal Relatives in Two Chinese Families
Jia Qu et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2010)
Leber's hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation
Min Liang et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2009)
Geneenvironment interactions in Leber hereditary optic neuropathy
Matthew Anthony Kirkman et al.
BRAIN (2009)
The novel G10680A mutation is associated with complete penetrance of the LHON/T14484C family
Juhua Yang et al.
MITOCHONDRION (2009)
Extremely Low Penetrance of Leber's Hereditary Optic Neuropathy in 8 Han Chinese Families Carrying the ND4 G11778A Mutation
Jia Qu et al.
OPHTHALMOLOGY (2009)
Investigation of auditory dysfunction in Leber hereditary optic neuropathy
Patrick Yu-Wai-Man et al.
ACTA OPHTHALMOLOGICA (2008)
A family with 3460G>A and 11778G>A mutations and haplogroup analysis of Polish Leber hereditary optic neuropathy patients
Katarzyna Tonska et al.
MITOCHONDRION (2008)
Sporadic Bilateral Optic Neuropathy in Children: The Role of Mitochondrial Abnormalities
Thomas M. Bosley et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2008)
Epidemiology and penetrance of Leber hereditary optic neuropathy in Finland
Anu Puomila et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2007)
The coexistence of mitochondrial ND6 T14484C and 12S rRNA A1555G mutations in a Chinese family with Leber's hereditary optic neuropathy and hearing loss
Qi-Ping Wei et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2007)
Male prevalence of acquired color vision defects in asymptomatic carriers of Leber's hereditary optic neuropathy
Dora Fix Ventura et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2007)
Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation -: A case report
Manuela M. Grazina et al.
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY (2007)
Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family
Jia Qu et al.
MITOCHONDRION (2007)
Leber's hereditary optic neuropathy with childhood onset
Piero Barboni et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2006)
Leber's hereditary optic neuropathy with dystonia in a Japanese family
M Watanabe et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2006)
Leber's hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families
XT Zhou et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)
The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation
J Qu et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2006)
Long-term follow-up of two sisters with Leber's hereditary optic neuropathy
T Yokoyama et al.
JAPANESE JOURNAL OF OPHTHALMOLOGY (2006)
Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder
G Hudson et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
A new sequence variant in mitochondrial DNA associated with high penetrance of Russian Leber hereditary optic neuropathy
N Povalko et al.
MITOCHONDRION (2005)
Ladies with Leber's hereditary optic neuropathy: an atypical disease
SS Dandekar et al.
EUROPEAN JOURNAL OF OPHTHALMOLOGY (2002)
Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population
CF Dogulu et al.
EYE (2001)
The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy
PF Chinnery et al.
BRAIN (2001)