Neuro-ophthalmology of mitochondrial diseases

Current Opinion in Ophthalmology

Volumn 11, Issue 6, 2000, Pages 408-412

  Riordan Eva, Paul ^a  

^a KING S COLLEGE HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

AGING; ARTICLE; DIAGNOSTIC IMAGING; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DNA POLYMORPHISM; ENCEPHALOMYOPATHY; GENE MUTATION; HEARING IMPAIRMENT; HUMAN; LEBER CONGENITAL AMAUROSIS; MATERNAL DIABETES MELLITUS; NEUROOPHTHALMOLOGY; PATHOGENESIS; PRIORITY JOURNAL; RETINA INJURY; RETINA MACULA DEGENERATION;

AGING; DIAGNOSIS, DIFFERENTIAL; DIAGNOSTIC IMAGING; DNA, MITOCHONDRIAL; HUMANS; MITOCHONDRIAL MYOPATHIES; MUTATION; OPTIC ATROPHIES, HEREDITARY; POLYMORPHISM, GENETIC; RETINAL DISEASES;

EID: 0033674402     PISSN: 10408738     EISSN: None     Source Type: Journal    
DOI: 10.1097/00055735-200012000-00005     Document Type: Article

References (20)

1. Mitochondrial DNA analysis: Polymorphisms and pathogenicity
2. Leber hereditary optic neuropathy (LHON): A mitochondrial disease with unresolved complexities
3. Predominance of the T14484C mutation in French-Canadian families with Leber hereditary optic neuropathy is due to a founder effect
4. Leber's hereditary optic neuropathy: Clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene
5. A new mitochondrial DNA mutation in the tRNA leucine 1 gene (C3275A) in a patient with Leber's hereditary optic neuropathy
6. Late onset of Leber's hereditary optic neuropathy in HIV infection
7. A pedigree of Leber's hereditary optic neuropathy with visual loss in childhood, primarily in girls
8. Comparing pupil function with visual function in patients with Leber's hereditary optic neuropathy
9. Comparison of threshold visual perimetry and objective pupil perimetry in clinical patients
10. Optic nerve enhancement on orbital magnetic resonance imaging in Leber's hereditary optic neuropathy
11. Retinopathy of NARP syndrome
12. Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation
13. Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness
14. Mitochondrial maculopathy: Geographic atrophy of the macula in the MELAS associated A to G 3243 mitochondrial DNA point mutation
15. Mitochondrial diseases in children: Neuroradiological and clinical features in 17 patients
16. MRI of the brain in the Kearns-Sayre syndrome: Report of four cases and a review
17. Mapping of autosomal dominant progressive external ophthalmoplegia to 1 7-cM critical region on 10q24
18. Autosomal dominant progressive external ophthalmoplegia: Distribution of multiple mitochondrial DNA deletions
19. The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS
20. Evaluation of bupivicaine-induced muscle regeneration in the treatment of ptosis in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome