Results 231 to 240 of about 10,615,218 (316)
Adams-Oliver Syndrome: A Clinical Diagnosis in the Genomic Era. [PDF]
Gl S +4 more
europepmc +1 more source
In patients with malignant ureteral obstruction undergoing percutaneous nephrostomy, sarcopenia defined by a low psoas muscle index was independently associated with poor overall survival on multivariate Cox regression analysis, suggesting that preoperative assessment of psoas muscle index may aid prognostic stratification in this population.
Kota Shimokihara +3 more
wiley +1 more source
Clinical Diagnosis and Treatment of 31 Children with <i>Mycoplasma pneumoniae</i> Necrotizing Pneumonia. [PDF]
Wang Z, Zhao Y, Liu H.
europepmc +1 more source
Cancer treatment is associated with measurable acceleration of biological aging across epigenetic, telomere, senescence, and immune biomarkers. However, biomarker validation and interventional strategies remain limited, especially in hematologic malignancies, underscoring the need for standardized multi‐omic aging assessments and adequately powered ...
Moataz Ellithi +3 more
wiley +1 more source
[Clinical diagnosis and treatment of four cases of Castleman disease in children]. [PDF]
Wu PQ +4 more
europepmc +1 more source
Elevated Connectivity During Language Processing Is Associated With Cognitive Performance in SeLECTS
ABSTRACT Objective Self‐Limited Epilepsy with Centrotemporal Spikes (SeLECTS) is associated with language impairments despite seizures originating in the motor cortex, suggesting aberrant cross‐network interactions. Here we tested whether functional connectivity in SeLECTS during language tasks predicts language performance.
Wendy Qi +8 more
wiley +1 more source
Chinese Guidelines for Clinical Diagnosis, Treatment, and Management of Cirrhosis (2025). [PDF]
Xu X +15 more
europepmc +1 more source
The Autopsy and Clinical Diagnosis
openaire +2 more sources
RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu +21 more
wiley +1 more source
Quantifying the impact of a computer-aided diagnostic score on the clinical diagnosis of functional seizures. [PDF]
Kerr WT +39 more
europepmc +1 more source

