Lisa Latchney
Overview
Explore the profile of Lisa Latchney including associated specialties, affiliations and a list of published articles.
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Articles
4
Citations
99
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0
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Recent Articles
1.
Tang C, Han J, Dalvi S, Manian K, Winschel L, Volland S, et al.
Commun Biol
. 2021 Feb;
4(1):161.
PMID: 33547385
Mutations in CLN3 lead to photoreceptor cell loss in CLN3 disease, a lysosomal storage disorder characterized by childhood-onset vision loss, neurological impairment, and premature death. However, how CLN3 mutations cause...
2.
Song H, Rossi E, Stone E, Latchney L, Williams D, Dubra A, et al.
Br J Ophthalmol
. 2017 Oct;
102(1):136-141.
PMID: 29074494
Purpose: Several genes causing autosomal-dominant cone-rod dystrophy (AD-CRD) have been identified. However, the mechanisms by which genetic mutations lead to cellular loss in human disease remain poorly understood. Here we...
3.
Song H, Rossi E, Latchney L, Bessette A, Stone E, Hunter J, et al.
JAMA Ophthalmol
. 2015 Aug;
133(10):1198-203.
PMID: 26247787
Importance: Stargardt disease (STGD1) is characterized by macular atrophy and flecks in the retinal pigment epithelium. The causative ABCA4 gene encodes a protein localizing to photoreceptor outer segments. The pathologic...
4.
Song H, Latchney L, Williams D, Chung M
JAMA Ophthalmol
. 2014 Jun;
132(9):1099-104.
PMID: 24922193
Importance: Fundus albipunctatus (FA) is a form of congenital stationary night blindness characterized by yellow-white spots, which were classically described as subretinal. Although night blindness and delayed dark adaptation are...