Results 171 to 180 of about 83,768 (248)
ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli +18 more
wiley +1 more source
Innovation, evidence and uncertainty: rethinking the evaluation of neurovascular devices. [PDF]
Taschner CA +4 more
europepmc +1 more source
Abstract INTRODUCTION Fluorodeoxyglucose (FDG) positron emission tomography (PET) is widely used for detecting metabolic changes associated with neurodegeneration in Alzheimer's disease (AD) and other dementias but is costly and involves ionizing radiation. Here we developed SynthPET, a multimodal deep learning framework that synthesizes FDG PET images
Xavier Beltran‐Urbano +15 more
wiley +1 more source
MRI Mapping in Meningioma: A Clinical Perspective on Presentation and Management. [PDF]
Todea RA.
europepmc +1 more source
Objective The objective of this study was to investigate the ability of patient‐reported/administered outcomes to capture disability worsening and progression independent of relapse activity (PIRA) in multiple sclerosis (MS). Methods We included patients from the longitudinal multicenter MS PATHS cohort with ≥3 assessments and >6 months follow‐up. PIRA
Evy M. Reinders +40 more
wiley +1 more source
Fluoroscopy-Guided Lumbar Puncture Training: Needs Assessment for Alternative Teaching Methods Including Simulation. [PDF]
Yang CW +3 more
europepmc +1 more source
Workflow for comparing three LLMs in radiographic anatomical identification using 30 radiographs and 196 anatomy questions across Normal and Thinking modes, with expert scoring and temporal consistency analysis. Abstract This study compared the performance of three large language models, ChatGPT‐5 Plus, Gemini 2.5 Pro, and SuperGrok 4, in identifying ...
Ismail Sivri +4 more
wiley +1 more source
ABSTRACT Sickle cell disease (SCD) with hemoglobin‐ (Hb‐) SC genotype is often considered a milder SCD variant, yet life‐threatening complications can occur. A 26‐year‐old man with HbSC disease presented with an infection triggered vaso‐occlusive crisis (VOC), acute chest syndrome (ACS), severe thrombocytopenia, Coombs‐negative hemolysis with ...
Benjamin Vieten +9 more
wiley +1 more source
Neuro Optical Coherence Tomography Guided Mechanical Thrombectomy. [PDF]
Forestier G +4 more
europepmc +1 more source
This study identified two metabolically distinct thrombus molecular subtypes in AIS: a lipid metabolism‐enriched subtype (C1) associated with cardioembolic stroke and poor functional outcomes, and a folate metabolism‐enriched subtype (C2) linked to atherothrombotic stroke and better prognosis. A six‐metabolite signature further demonstrated exploratory
Taoyuan Lu +7 more
wiley +1 more source

