Results 231 to 240 of about 148,827 (308)
Kramers-Kronig Diagnostic of Humidity-Induced Non-Idealities in Nanostructured Silica Capacitors. [PDF]
Véliz B +4 more
europepmc +1 more source
MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children
ABSTRACT Objectives The study aimed to characterize the clinical features, etiologies, and outcomes of isolated, first‐time pediatric ON in the post‐MOG‐IgG era. Methods This was a single‐center retrospective cohort study at Texas Children's Hospital of patients diagnosed with first‐time ON between 2018–2024, with follow‐up data collected through 2025.
Chaitanya Aduru +13 more
wiley +1 more source
Diabetic Peripheral Neuropathy: Mechanisms and Emerging Therapies. [PDF]
Albariqi MMH +6 more
europepmc +1 more source
Clinical Impact of NOTCH3 Variant Location After First Stroke in CADASIL
ABSTRACT Objective Despite its monogenic origin, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy exhibits marked variability in clinical expression and severity. Variants in the NOTCH3 gene, within epidermal growth factor‐like repeat domains 1–6 or 7–34, are known to influence disease onset, but their impact ...
Léa Aguilhon +5 more
wiley +1 more source
Clinical and electrophysiological features for differentiating MMN from hand-onset ALS. [PDF]
Fang SY +7 more
europepmc +1 more source
ABSTRACT Objective Digital technologies hold promise for transforming healthcare by enhancing personalized treatments and offer valuable opportunities to improve patient care. Here, we evaluated several novel, self‐administered, home‐based, digital endpoints for their association with corresponding conventional standard clinical measures (primary) in ...
Arne Mueller +14 more
wiley +1 more source
Multilayer Carbon-Structured BaTiO<sub>3</sub>@C Nanocomposites with Wide Microwave Absorption Bandwidth and Excellent Corrosion Resistance. [PDF]
Guo S, Sun Y, Li S, Jiang X, Sun D.
europepmc +1 more source
ABSTRACT Objective Variants in SLC6A1, encoding the GABA transporter 1 (GAT‐1), cause epilepsy, autism spectrum disorder, and developmental delay via loss of GABA uptake, impaired trafficking, and ER retention. We previously found that 4‐Phenylbutyrate (PBA), an FDA‐approved drug, restores GABA uptake and reduces seizures in SLC6A1‐related disorders ...
Melissa B. DeLeeuw +5 more
wiley +1 more source
Recurrent Syncope and Ventricular Standstill Due to Phase 4 His-Purkinje Block. [PDF]
Ahmad F, Lo CCW, Youssef G, Ilsar R.
europepmc +1 more source

