Leber’s optic neuropathy associated with disseminated white matter disease: A case report and review
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,General Medicine,Surgery
Reference16 articles.
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2. Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation;Harding;Am J Hum Genet,1995
3. Occurrence of a multiple sclerosis-like illness in women who have a Leber’s hereditary optic neuropathy mitochondrial DNA mutation;Harding;Brain,1992
4. Visual recovery in a man with the rare combination of mtDNA 11778 LHON mutation and a MS-like disease after mitoxantrone therapy;Buhmann;Acta Neurol Scand,2002
5. Clinical and brain bioenergetics improvement with idebenone in a patient with Leber’s hereditary optic neuropathy: a clinical and 31P-MRS study;Cortelli;J Neurol Sci,1997
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1. A Comprehensive Review of Leber Hereditary Optic Neuropathy and Its Association with Multiple Sclerosis-Like Phenotypes Known as Harding’s Disease;Eye and Brain;2024-07
2. Presence of palinopsia as a sign of selective CNS tractopathy: A case report;Revista Científica de la Sociedad Española de Enfermería Neurológica;2023-12
3. Leber’s Hereditary Optic Neuropathy Plus Causing Recurrent Myelopathy due to an MT-DN1 Mutation at G3635A;Case Reports in Neurological Medicine;2022-01-11
4. Mitochondrial Mutations in Multiple Sclerosis Patients with Atypical Optic Neuropathy;Multiple Sclerosis and Related Disorders;2021-10
5. Occult primary white matter impairment in Leber hereditary optic neuropathy;European Journal of Neurology;2021-07-09
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