Spinal cord involvement in LHON requires pathophysiological clarification
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology,General Medicine
Reference10 articles.
1. Late-onset Leber’s hereditary optic neuropathy presenting with longitudinally extensive myelitis harbouring the m.14484T>C mutation: extending the genotype-phenotype spectrum;Cleaver;Mult. Scler. Relat. Disord.,2020
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3. Leber’s hereditary optic neuropathy associated with multiple sclerosis: harding’s syndrome;Parry-Jones;Pract. Neurol.,2008
4. Affection of immune cells by a C10orf2 mutation manifesting as mitochondrial myopathy and transient sensory transverse syndrome;Finsterer;Acta Neurol. Belg.,2017
5. Leber hereditary optic neuropathy plus dystonia, and transverse myelitis due to double mutations in MT-ND4 and MT-ND6;Berardo;J. Neurol.,2020
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