Results 71 to 80 of about 8,751 (287)
Oman Journal of Ophthalmology, 2021 BACKGROUND: Treating congenital blepharoptosis is often mandatory to clear the visual access and avoid amblyopia; however, when the levator function is poor, achieving a satisfactory long-term outcome is challenging.
A. Dawood +2 more
semanticscholar +1 more source
PDK4 and nutrient responses explain muscle specific manifestation in mitochondrial disease
Clinical and Translational Medicine, Volume 15, Issue 7, July 2025.Mitochondrial disease triggers opposite responses in different muscles. Mitochondrial integrated stress response (ISRmt) and aerobic glycolysis characterize large muscles. Eye muscles show no ISRmt but activate PDK4—inhibitor of glucose oxidation—thereby upregulating beta‐oxidation, which is non‐optimal in mitochondrial disease and can explain eye ...
Swagat Pradhan +6 more
wiley +1 more source
PLoS ONE, 2021 In this study, we aimed to evaluate the characteristics of astigmatism preoperatively and 1 month postoperatively in patients with age-related ptosis (AP) and contact lens-related ptosis (CLP), and investigate surgery-induced astigmatism (SIA) using the ...
Kazuhiko Dannoue +4 more
semanticscholar +1 more source
中西医结合护理, 2022 This paper summarized the whole process of nursing intervention for a patient with oculomotor paralysis caused by systemic lupus erythematosus. Responsible nurses were involved throughout the process, in which overall evaluation of disease condition ...
LI Yuncui (李运翠) +4 more
doaj +1 more source
Quantitative analysis of the eyelid curvature in patients with blepharoptosis. [PDF]
BMC Med ImagingKhalili Pour E +4 more
europepmc +3 more sources
Targeted next-generation sequencing of dedifferentiated chondrosarcoma in the skull base reveals combined TP53 and PTEN mutations with increased proliferation index, an implication for pathogenesis [PDF]
, 2016 Dedifferentiated chondrosarcoma (DDCS) is a rare disease with a dismal prognosis. DDCS consists of two morphologically distinct components: the cartilaginous and noncartilaginous components.
Cao, Dengfeng +13 more
core +2 more sources
Clinical and Translational Medicine, Volume 15, Issue 6, June 2025.OXA1L gene bi‐allelic variants cause mitochondrial myopathy. OXA1L deficiency results in combined mitochondrial respiratory chain defects and OXPHOS impairments. OXA1L deficiency leads to elevated ROS production, which may activate the NF‐κB signalling pathway, disturbing myogenic gene expression and triggering cell apoptosis. Abstract Background OXA1L
Yongkun Zhan +11 more
wiley +1 more source
Lemierre Syndrome with Blepharoptosis
Internal Medicine, 2010 A 51-year-old woman was hospitalized with a high fever, occipital pain, blepharoptosis, and trismus. Enhanced CT showed thrombophlebitis of her left cavernous sinus, maxillary vein, and multiple pulmonary nodular lesions. (18)F-FDG PET/CT showed significant uptakes in the same lesions. Streptococcus constellatus was detected in her blood.
Misa Nakano +9 more
openaire +4 more sources
The role of apoptosis in blepharoptosis [PDF]
Eye, 2013 The purpose of this study is to evaluate the role of apoptosis in the pathogenesis of blepharoptosis.Forty-five eyelids of 43 consecutive patients (16 female, 27 males) that underwent levator resection surgery for ptosis correction were included in the study.
Güler Zilelioğlu +4 more
openaire +3 more sources
Ophthalmic Plastic and Reconstructive Surgery, 2021 Purpose: To review and evaluate the efficacy and complication rates of external and internal blepharoptosis repair techniques in pediatric patients. Methods: The systematic review protocol was published on PROSPERO (CRD42020197343).
Hong Kai Lim +3 more
semanticscholar +1 more source