Results 121 to 130 of about 55,222 (253)
Analysis of Pediatric Secondary Glaucoma Patients Treated with Micropulse Transscleral Cyclophotocoagulation (MP-TSCPC). [PDF]
Wójcik-Niklewska B +7 more
europepmc +1 more source
Astrocytes are key sensors and transducers of biomechanical stimuli within the central nervous system. Astrocyte development is highly dependent on mechanical stimuli such as surrounding tissue stiffness and biomechanical strain. Mechanosensory pathways including integrins, connexins and pannexins, and mechanosensitive channels regulate astrocyte ...
Ana N. Strat +3 more
wiley +1 more source
Iris Metastasis of Pancreatic Cancer Presenting with Hyphema and Secondary Glaucoma: A Case Report. [PDF]
Jeon H, Hwang JY, Jo YJ, Choe S.
europepmc +1 more source
A comparative study of ultrasound cycloplasty and endoscopic cyclophotocoagulation in the treatment of secondary glaucoma. [PDF]
Ruixue W +6 more
europepmc +1 more source
Abstract Introduction Pre‐eclampsia (PE) involves systemic endothelial dysfunction and microvascular injury, yet routine obstetric care lacks noninvasive readouts of maternal microvascular health. We evaluated whether hypertensive retinopathy (HR) detected during pregnancy is associated with maternal disease severity and adverse neonatal outcomes ...
Gabriele Saccone +6 more
wiley +1 more source
Etiology and clinical analysis of secondary glaucoma: a single-center study from northwest China. [PDF]
Liu Y +8 more
europepmc +1 more source
ABSTRACT Propionic acidemia (PA) is a rare inherited metabolic disorder associated with recurrent metabolic decompensations and chronic multisystemic complications. Liver transplantation (LT) may improve metabolic stability, but its long‐term impact on organ involvement remains debated.
Tristan Mekdade +25 more
wiley +1 more source
Secondary Glaucoma Resulting From Choroidal Melanoma in a Patient With Congenital Nevus of Ota. [PDF]
Petchyim S +3 more
europepmc +1 more source
We have identified 4 pathogenic/likely pathogenic changes and 2 variants of uncertain significance, 3 of which were novel. The identification of disease‐causing variants in the CRYAA, MYH9, RP2, and CLNC1 genes allowed us to establish an accurate genetic diagnosis of inherited cataract and to describe overlapping clinical phenotypes.
Kristiyana Vitanova +10 more
wiley +1 more source
Purpureocillium lilacinum Keratitis and Endophthalmitis in an Aphakic Eye With Secondary Glaucoma: A Case Report. [PDF]
Tsirogianni N +4 more
europepmc +1 more source

