Results 111 to 120 of about 41,612 (247)
Choroidal neovascularization in an adolescent with RDH12-associated retinal degeneration
, 2019 © 2019, © 2019 Taylor & Francis Group, LLC. Background: Leber congenital amaurosis (LCA) due to RDH12 mutations typically manifests with severe vision loss and panretinal dystrophy.
Tsang, S. H. +5 more
core +1 more source
The Journal of Physiology, EarlyView.Abstract figure legend Mitochondria are highly dynamic organelles that continuously remodel their architecture through coordinated cycles of fusion and fission. This review examines the four key GTPases that orchestrate mitochondrial dynamics in mammals: MFN1, MFN2, OPA1, and DRP1.
Rémi Chaney +4 more
wiley +1 more source
Automatic detection of the retinal neovascularization in diabetic patients.
, 2014 International audiencePurpose: Diabetes is a major pathology of which the prevalence is increasing worldwide. The retinal neovascularization related to diabetes is a major cause of blindness.
Leveziel, Nicolas +5 more
core +2 more sources
Reduced Retinal Neovascularization.
, 2015 The effect of emixustat on retinal neovascularization was studied in the mouse OIR model. Seven day-old mouse pups were subjected to hyperoxia (75% oxygen) for 5 days. On P12, the mice were returned to room air and daily treatments with ruboxistaurin (10
Kyoko Mitts (738271) +14 more
core +1 more source
Mechanisms of retinal and choroidal neovascularization.
Investigative ophthalmology & visual science, 1994 Version of ...
openaire +2 more sources
Airway Involvement in Conradi–Hünermann–Happle Syndrome: A Novel Clinical Manifestation
The Laryngoscope, Volume 136, Issue 7, Page 3240-3245, July 2026.We report the first documented case of airway involvement in Conradi–Hünermann–Happle syndrome (CDPX2), an X‐linked dominant form of chondrodysplasia punctata caused by pathogenic variants in EBP. A 2‐month‐old female with genetically confirmed CDPX2 developed severe subglottic stenosis and persistent respiratory distress requiring CPAP; cross ...
Enrique G. Villarreal +3 more
wiley +1 more source
, 2010 PURPOSE: To determine whether different coagulation-balance genetic polymorphisms explain the variable clinical outcomes of photodynamic therapy with verteporfin (PDT-V) in Caucasian patients with classic or predominantly classic choroidal ...
Romano, Mario
core
A Rare Cause of Type II Neovascularization: Unilateral Retinal Pigment Epithelium Dysgenesis
, 2020 Unilateral retinal pigment epithelium dysgenesis (URPED) is a very rare clinical condition first described in 2002. Fundus examination and imaging findings are almost pathognomonic and can facilitate diagnosis of this uncommon disease.
Berrak Şekeryapan Gediz
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Diabetes, Obesity and Metabolism, Volume 28, Issue 7, Page 5614-5626, July 2026.ABSTRACT Aims Diabetic retinopathy (DR) is linked to elevated risks of cerebrovascular diseases. Whether sodium‐glucose cotransporter‐2 inhibitors (SGLT2i) reduce stroke risk in patients with type 2 diabetes (T2D) and DR remains uncertain. Materials and Methods We conducted a retrospective cohort study using the TriNetX Research Network.
Kuo‐En Chen +3 more
wiley +1 more source
Natriuretic Peptides and the Regulation of Retinal Neovascularization [PDF]
Arteriosclerosis, Thrombosis, and Vascular Biology, 2020 Burtenshaw, Denise, Cahill, Paul A.
openaire +4 more sources