Search research articles
Contact Us
Filters
Showing results (121-130 of 183) with videos related to
Page
of 19
Sort By:
Progress in Retinal and Eye Research
|
December 19, 2020
Dominant optic atrophy: Culprit mitochondria in the optic nerve
Guy Lenaers, Albert Neutzner, Yannick Le Dantec, et al.
Investigative Ophthalmology & Visual Science
|
February 19, 2010
Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO
Laura C Greaves, Patrick Yu-Wai-Man, Emma L Blakely, et al.
Frontiers in Neuroscience
|
November 2, 2020
Optical Coherence Tomography Angiography Reveals Distinct Retinal Structural and Microvascular Abnormalities in Cerebrovascular Disease
Xiayin Zhang, Hui Xiao, Chunxin Liu, et al.
Annals of Neurology
|
February 6, 2015
Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease
Gráinne S Gorman, Andrew M Schaefer, Yi Ng, et al.
Survey of Ophthalmology
|
April 30, 2026
Omics in hereditary optic neuropathies:A systematic review of clinical studies with an integrated point of view
Raoul K Khanna, Xuehao Cui, David Chuen Soong Wong, et al.
Neurology. Genetics
|
April 29, 2016
Homozygous deletion in MICU1 presenting with fatigue and lethargy in childhood
David Lewis-Smith, Kimberli J Kamer, Helen Griffin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 1, 2023
Optic Disc and Retinal Architecture Changes in Patients with Spinocerebellar Ataxia Type 2
Flávio Moura Rezende Filho, Neringa Jurkute, João Brainer Clares de Andrade, et al.
Plos One
|
October 3, 2013
Extraocular muscle atrophy and central nervous system involvement in chronic progressive external ophthalmoplegia
Cynthia Yu-Wai-Man, Fiona E Smith, Michael J Firbank, et al.
The British Journal of Ophthalmology
|
May 21, 2020
Comparison of macular structural and vascular changes in neuromyelitis optica spectrum disorder and primary open angle glaucoma: a cross-sectional study
Xiayin Zhang, Hui Xiao, Chunxin Liu, et al.
Journal of Medical Genetics
|
November 13, 2015
Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation
Ronen Spiegel, Ann Saada, Padraig J Flannery, et al.
Page
of 19
Search research articles
Search
Showing results (121-130 of 183) with videos related to
Sort By:
Page
of 19
Progress in Retinal and Eye Research
|
December 19, 2020
Dominant optic atrophy: Culprit mitochondria in the optic nerve
Guy Lenaers, Albert Neutzner, Yannick Le Dantec, et al.
Investigative Ophthalmology & Visual Science
|
February 19, 2010
Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO
Laura C Greaves, Patrick Yu-Wai-Man, Emma L Blakely, et al.
Frontiers in Neuroscience
|
November 2, 2020
Optical Coherence Tomography Angiography Reveals Distinct Retinal Structural and Microvascular Abnormalities in Cerebrovascular Disease
Xiayin Zhang, Hui Xiao, Chunxin Liu, et al.
Annals of Neurology
|
February 6, 2015
Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease
Gráinne S Gorman, Andrew M Schaefer, Yi Ng, et al.
Survey of Ophthalmology
|
April 30, 2026
Omics in hereditary optic neuropathies:A systematic review of clinical studies with an integrated point of view
Raoul K Khanna, Xuehao Cui, David Chuen Soong Wong, et al.
Neurology. Genetics
|
April 29, 2016
Homozygous deletion in MICU1 presenting with fatigue and lethargy in childhood
David Lewis-Smith, Kimberli J Kamer, Helen Griffin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 1, 2023
Optic Disc and Retinal Architecture Changes in Patients with Spinocerebellar Ataxia Type 2
Flávio Moura Rezende Filho, Neringa Jurkute, João Brainer Clares de Andrade, et al.
Plos One
|
October 3, 2013
Extraocular muscle atrophy and central nervous system involvement in chronic progressive external ophthalmoplegia
Cynthia Yu-Wai-Man, Fiona E Smith, Michael J Firbank, et al.
The British Journal of Ophthalmology
|
May 21, 2020
Comparison of macular structural and vascular changes in neuromyelitis optica spectrum disorder and primary open angle glaucoma: a cross-sectional study
Xiayin Zhang, Hui Xiao, Chunxin Liu, et al.
Journal of Medical Genetics
|
November 13, 2015
Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation
Ronen Spiegel, Ann Saada, Padraig J Flannery, et al.
Page
of 19