Understanding Capsular Contraction and IOL Decentration in Toric and EDOF Lenses: Clinical and Biomechanical Insights. [PDF]
Gurnani B, Kaur K.
europepmc +1 more source
Musculoskeletal humanoids exhibit rich biomechanical properties that remain insufficiently unified in prior discussions. This article systematically categorizes muscle characteristics into five properties: redundancy, independency, anisotropy, variable moment arm, and nonlinear elasticity, and analyzes their combined effects on control.
Kento Kawaharazuka +2 more
wiley +1 more source
Uveitis-Glaucoma-Hyphema Syndrome Secondary to Asymmetric Intraocular Lens (IOL) Haptic Fixation: A Clinical Lesson in Mechanism-Based Diagnosis and Treatment. [PDF]
Bonifazi T, Tanito M.
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ABSTRACT Background Outdoor agricultural workers experience significant heat exposure, yet few studies have evaluated whether wearable sensors can reliably measure continuous physiological responses in real field conditions. This pilot study examined the feasibility and predictive utility of core temperature, hydration, heart rate, and movement data ...
Sinan Sousan +10 more
wiley +1 more source
Modified 3-piece intraocular lens of iris fixation technique in the management of cases without capsular support: Sutureless iris fixation (Dağ technique). [PDF]
Dağ U +4 more
europepmc +1 more source
Melatonin Levels in 89 Individuals With Smith Magenis Syndrome
ABSTRACT In patients with Smith–Magenis syndrome (SMS), an inverted circadian rhythm of melatonin (MT) contributes to the sleep disturbance. Standard treatment of sleep disturbance with MT often leads to extremely high daytime MT levels, resulting in even more sleep disorders. We therefore retrospectively evaluated the MT data of 89 SMS patients.
Wiebe Braam, Ann C. M. Smith
wiley +1 more source
Characterization of the Fiber Protein C-Terminal Domain from <i>Klebsiella pneumoniae</i> Phage KlebP_144 and Evaluation of Its Anti-Capsular Activity. [PDF]
Kravchuk BI +8 more
europepmc +1 more source
ABSTRACT Autosomal recessive HARS1‐related disorder (originally described as Usher syndrome type 3B) caused by a homozygous Y454S variant in the histidyl‐tRNA synthetase gene (HARS1) is characterized by progressive sensorineural hearing and vision loss and respiratory deterioration with risk for sudden death following febrile illnesses.
Victoria Mok Siu +23 more
wiley +1 more source
DPSCs, hepatocytes, and exosomes were tested for liver fibrosis therapy. Exosome‐based treatment exhibited superior antioxidative and regenerative effects. Liver enzymes, oxidative stress, and profibrotic markers were significantly reduced. α‐SMA, desmin, and related gene expression were downregulated.
Sahar Rahimi +3 more
wiley +1 more source
Reply : Anchor-assisted capsular bag IOL implantation to correct subluxated lenses in children with Marfan syndrome: long-term follow-up. [PDF]
Yehezkeli V +5 more
europepmc +1 more source

