Results 161 to 170 of about 309,795 (229)

Prenatal Ultrasound Diagnosis and Prognosis Analysis of Fetal Congenital Cataract. [PDF]

Int J Womens Health
Wang H, Jin X, Wang M, Li H, Wu J, Liu L, Zhu Z, Qiao M, Wang Y, Li L.   +9 more
europepmc   +1 more source

Erratum in: A Novel CRYBB2 Splicing Mutation Is Associated With Lens Extracellular Matrix Remodeling and Vascular Alterations in Congenital Cataract. [PDF]

Invest Ophthalmol Vis Sci
europepmc   +1 more source

Perception of Congenital Cataract among Saudi Parents in Saudi Arabia. [PDF]

Ann Afr Med
Aljaafari AM, Al-Mulla AT, Alsowaigh SS, Al-Medires MA, Alotaibi HA, Alarfaj AA, Aljaafari AM, Al Taisan AA, Ali SI.   +8 more
europepmc   +1 more source

Comparison of outcomes after early congenital cataract surgery in eyes with/without microcornea. [PDF]

Int J Ophthalmol
Zhang F, Li ZL, Wu JY, Zhao YE.
europepmc   +1 more source

Dynamics of Anterior Chamber Angle Parameters in Primary and Secondary Pseudophakic Eyes Following Congenital Cataract Surgery. [PDF]

Transl Vis Sci Technol
Li S, Wu J, Wang D, Zhang R, Zhao Y, Zhang H, Ding X, Chang P, Zhao YE.   +8 more
europepmc   +1 more source

Risk factors for capsular phimosis following congenital cataract extraction. [PDF]

J AAPOS
Al-Lozi AM, McFadyen J, Shue A, Lambert SR.   +3 more
europepmc   +1 more source

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

Identification and functional characterization of a novel CRYBB1 deletion mutation causing autosomal dominant congenital cataract in a Chinese family. [PDF]

BMC Ophthalmol
Li L, Yue J, Song J, Qin M, Zhou S, Liu J, Zheng G.   +6 more
europepmc   +1 more source

Benchmarking large language models for congenital cataract parent counseling: safety, readability, and knowledge translation of developmental and genetic information. [PDF]

Front Cell Dev Biol
Jiang L, Zhu Y, Song C, Hu X, Fan X, Yang W, Zhao Y.   +6 more
europepmc   +1 more source

Abnormal Splicing in the Final Intron of PRX Results in Dominant Congenital Cataract Without Neurological Phenotype. [PDF]

Invest Ophthalmol Vis Sci
Reis LM, Bellingham J, Motta FL, Jurkute N, Raskin S, Ramos F, Mahroo OA, Moosajee M, Arno G, Semina EV.   +9 more
europepmc   +1 more source