Ophthalmological phenotype associated with homozygous null mutation in the NEUROD1 gene [PDF]
Balogh, István +7 more
core
Utilization of an automated machine learning approach for the detection of granular corneal dystrophy via slit lamp photographs. [PDF]
Yavari N +18 more
europepmc +1 more source
CRISPR Base Editing Correction of TGFBI Mutations in Autosomal Dominant Corneal Dystrophies. [PDF]
Chen J +10 more
europepmc +1 more source
A Rare Case of Fluoxetine-Induced Vortex Keratopathy. [PDF]
Behera S, Sahu S, Pilani S, V A.
europepmc +1 more source
Case Report: Post-LASIK exacerbation of granular corneal dystrophy type 2: a familial case with <i>TGFBI</i> mutation. [PDF]
Kuang L +6 more
europepmc +1 more source
Genetic epidemiology of epithelial-stromal TGFBI dystrophies in a large Korean population. [PDF]
Cho EH, Lee M, Ki CS, Seol CA, Jang MA.
europepmc +1 more source
Anatomically Guided Non-Viral CRISPR/Cas9 Delivery in the Eye: Overcoming Barriers for Precision Gene Therapy. [PDF]
Hua Z, Shen Y, Zhou X.
europepmc +1 more source
Comparison of corneal thickness measured using the new Revo FC optical coherence tomographer and the pentacam Scheimpflug-based imaging system. [PDF]
Tubis J, Zajączkowska Z, Kanclerz P.
europepmc +1 more source
Changing Trends in Childhood Blindness in Schools for the Visually Impaired in India: A Structured Literature Review. [PDF]
Agarwal P, Chauhan L.
europepmc +1 more source
Integrating AI, imaging innovations and omics for precision medicine. [PDF]
Jin K, Shi D, Zhang J.
europepmc +1 more source

