Results 251 to 260 of about 310,806 (291)

Utilization of an automated machine learning approach for the detection of granular corneal dystrophy via slit lamp photographs. [PDF]

BMC Ophthalmol
Yavari N, Mohammadi SS, Sokol JT, Feky DE, Rajabi M, Hung JH, Or C, Elaraby O, Anover FA, Saengsirinavin AO, Akhavanrezayat A, Mobasserian A, Than NTT, Guo J, Bai Y, Yasar C, Afshari NA, Lin CC, Nguyen QD.   +18 more
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Tips of family history taking in diagnosing Alport syndrome: a report of six cases. [PDF]

CEN Case Rep
Mori T.
europepmc   +1 more source

Advanced therapies for inherited optic neuropathies. [PDF]

Eye (Lond)
Wong DCS, Makam R, Yu-Wai-Man P.
europepmc   +1 more source

Immediate sequential bilateral retinal detachment repair in a patient with suspected COL2A1 and APC mutations. [PDF]

J Vitreoretin Dis
Arias-González N, Kiryakoza L, Fernandez MP, Negron CI, Lopez-Cañizares A, Malek DA, Berrocal AM.   +6 more
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Identification of co-segregating GJA3 and CRYBA1 missense variants in a Chinese family with congenital cataract: a possible digenic etiology. [PDF]

Front Med (Lausanne)
Zhou C, Li K, Zhou Z, Jian S, Jin L, Wang C, Zhang X.   +6 more
europepmc   +1 more source

Application of Machine Learning to Discriminate Photoreceptor Cell Species in Xenotransplanted Chimeric Retinas. [PDF]

Clin Transl Sci
Li KV, Pan A, Liu YV, Antonio-Aguirre B, Wang J, Adams M, McNerney C, Tun SBB, Jimenez K, Lu Y, Li Z, McNally M, Barathi VA, Johnston RJ, Singh MS.   +14 more
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A multicenter retrospective evaluation of the prevalence of known and presumed hereditary eye diseases in Lagotto Romagnolo dog breed within a referral population in Italy (2012-2020).

Veterinary Ophthalmology, 2022
OBJECTIVE To describe the ophthalmological findings of Lagotto Romagnolo dog breed and to report the prevalence of Known and Presumed Hereditary Eye Diseases (KP-HED).
M. Crasta, K. Arteaga, L. Barachetti, A. Guandalini   +3 more
semanticscholar   +1 more source

Risk of eye diseases in osteogenesis imperfecta - A nationwide, register-based cohort study.

Bone, 2021
BACKGROUND Osteogenesis imperfecta (OI) is a hereditary disease caused by affected collagen type 1. Collagen type 1 is an important structural component of the eye.
M. Lyster, J. Hald, M. Rasmussen, J. Grauslund, L. Folkestad   +4 more
semanticscholar   +1 more source

Non-infectious and non-hereditary diseases of the corneal epithelium.

Experimental Eye Research, 2020
The corneal epithelium serves as a physical barrier and a refractive element. Therefore, diseases of the corneal epithelium can increase the risk for infection and causes vision loss.
K. Voss, Annie Nguyen, M. Heur
semanticscholar   +1 more source