Neuroanatomical Changes in Leber’s Hereditary Optic Neuropathy: Clinical Application of 7T MRI Submillimeter Morphometry

Leber’s hereditary optic neuropathy (LHON) is one of the mitochondrial diseases that causes loss of central vision, progressive impairment and subsequent degeneration of retinal ganglion cells (RGCs). In recent years, diffusion tensor imaging (DTI) studies have revealed structural abnormalities in v...

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Detalles Bibliográficos
Autores principales: Jonak, Kamil, Krukow, Paweł, Symms, Mark, Maciejewski, Ryszard, Grochowski, Cezary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7348858/
https://www.ncbi.nlm.nih.gov/pubmed/32526981
http://dx.doi.org/10.3390/brainsci10060359

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7348858/
https://www.ncbi.nlm.nih.gov/pubmed/32526981
http://dx.doi.org/10.3390/brainsci10060359

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