Results 181 to 190 of about 152,478 (263)
Retrospective Study of 2-year Clinical Outcomes of Combination Ab-Interno Canaloplasty and a Microstent Compared to Ab-Interno Canaloplasty in Cataract Surgery Patients. [PDF]
Trubnik V, Huang L, Hall B.
europepmc +1 more source
Minimally Invasive Glaucoma Surgery: Is It Here to Stay?
ABSTRACT The advent of minimally invasive glaucoma surgery (MIGS) has expanded the treatment options available for glaucoma by providing options for reducing intraocular pressure without the serious complication profile associated with incisional glaucoma surgery.
Neeranjali Jain, Jennifer C. Fan Gaskin
wiley +1 more source
Pharmacological Strategies for Cataract Management: From Molecular Targets to Clinical Translation. [PDF]
de Diego-García L+3 more
europepmc +1 more source
Cerebrotendinous xanthomatosis is due to biallelic pathogenic variants in CYP27A1. We report a new patient and his good neurocognitive outcome on the chenodeoxycholic acid treatment despite therapy starting at the age of 34 years. This highlights the importance of recognizing treatable inherited metabolic diseases at any age.
Randa Sultan+6 more
wiley +1 more source
Childhood amblyopia in a tertiary eye care center in western India. [PDF]
Kelkar JA, Jain HH, Kelkar AS, Kelkar S.
europepmc +1 more source
Identification of Genetic Variants Causing Paediatric Cataract in Myanmar
Up to 60% of children with cataract in Myanmar have a causative variant in a known cataract gene. This is a similar rate to other populations screened to date, but highlights that there are more cataract genes left to identify. ABSTRACT Genetic testing for paediatric cataract detects a cause in 50%–70% of affected children but is as low as 20% in some ...
Johanna L. Jones+16 more
wiley +1 more source
Optimization of the Ocular Surface Prior to Cataract Surgery Using Cryopreserved Amniotic Membrane. [PDF]
Wongskhaluang J.
europepmc +1 more source
A SERIES OF CASES OF "GLASSBLOWERS' CATARACT" OCCURRING IN CHAINMAKERS
B. H. St. C. Roberts
openalex +1 more source
We report a 2‐year‐old male with clinical features of Takenouchi‐Kosaki syndrome, bilateral colobomas, and a de novo, likely pathogenic missense variant in CDC42. Supportive evidence includes a Cdc42 conditional knock‐out mouse model with colobomas.
Diana Brightman+11 more
wiley +1 more source