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Page 1
Congenital monocular elevation deficiency associated with a novel TUBB3 gene variant.
Thomas MG, Maconachie GDE, Constantinescu CS, Chan WM, Barry B, Hisaund M, Sheth V, Kuht HJ, Dineen RA, Harieaswar S, Engle EC, Gottlob I. Thomas MG, et al. Among authors: harieaswar s. Br J Ophthalmol. 2020 Apr;104(4):547-550. doi: 10.1136/bjophthalmol-2019-314293. Epub 2019 Jul 13. Br J Ophthalmol. 2020. PMID: 31302631 Free PMC article.
Dorsal midbrain (Parinaud) syndrome.
Prakash E, Kuht HJ, Harieaswar S, Thomas MG. Prakash E, et al. Among authors: harieaswar s. Pract Neurol. 2021 Dec;21(6):550-551. doi: 10.1136/practneurol-2021-003068. Epub 2021 Aug 25. Pract Neurol. 2021. PMID: 34433682 No abstract available.
Lipochoristoma: a rare cause of unilateral hearing loss.
Brahmbhatt K, Harieaswar S, Das S. Brahmbhatt K, et al. Among authors: harieaswar s. BMJ Case Rep. 2024 Oct 1;17(10):e259086. doi: 10.1136/bcr-2023-259086. BMJ Case Rep. 2024. PMID: 39353668