Harvard Catalyst Profiles

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Optic Atrophies, Hereditary

"Optic Atrophies, Hereditary" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, AUTOSOMAL DOMINANT) and Leber hereditary optic atrophy (OPTIC ATROPHY, HEREDITARY, LEBER).


This graph shows the total number of publications written about "Optic Atrophies, Hereditary" by people in Harvard Catalyst Profiles by year, and whether "Optic Atrophies, Hereditary" was a major or minor topic of these publication.
Bar chart showing 17 publications over 14 distinct years, with a maximum of 2 publications in 1990 and 1997 and 2001
To see the data from this visualization as text, click here.
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Funded by the NIH/NCATS Clinical and Translational Science Award (CTSA) program, grant number UL1TR001102, and through institutional support from Harvard University, Harvard Medical School, Harvard T.H. Chan School of Public Health, Beth Israel Deaconess Medical Center, Boston Children's Hospital, Brigham and Women's Hospital, Massachusetts General Hospital and the Dana Farber Cancer Institute.