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Vitreoretinal disease was the most common manifestation, of which cytomegalovirus retinitis (CMVR) was the most frequent retinal infection (overall prevalence 8.7%, 95% CI: 4.1-13.3%).
Branch retinal vein occlusion (BRVO) is the second most frequent retinal vascular disease with a prevalence rate of 0.3 1.1 % [ 1].
Our findings may be explained by the nature of the retinal events examined as the most frequent retinal end point was laser photocoagulation.
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The most frequent reported retinal findings in hyperviscosity syndrome are central retinal hemorrhages and vein dilation[ 2, 3].
Macular oedema secondary to retinal vein occlusion (RVO) is the second most frequent major retinal vascular disease after diabetic retinopathy and is also one of the most common causes of sudden visual loss [ 1, 2].
Retinitis pigmentosa (RP; MIM# 268,000) is the most frequent subtype of inherited retinal disease and is clinically and genetically a highly heterogeneous disorder [den Hollander at al., 2010].
Most frequent ocular manifestation was retinal periphlebitis, followed by periphlebitis together with inflammation of arteries (81.6% versus 65.0% at P = 0.03 < 0.05) (Table 5, Figure 1).
The most frequent ocular events were retinal pigment epithelial tear (27 patients, 0.61%) and intraocular pressure related events (12 patients, 0.27%) (table 2).
However, the most frequent type in Japan is retinal vasculitis, while the other types are rare.
In human, mutations in rhodopsin involving its intracellular mislocalization, are the most frequent cause of autosomal dominant Retinitis Pigmentosa, a degenerative retinal pathology characterized by progressive blindness.
Most frequent ocular manifestations in the examined group were retinal periphlebitis 81.6%, periphlebitis and periarteritis 65%, and serofibrinous uveitis 63.2%.
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