A bibliometric analysis of macrophages associated with chronic obstructive pulmonary disease from 2005 to 2025. [PDF]
Wang H +6 more
europepmc +1 more source
This work presents a deep learning model to autonomously recognize and classify the secretion retention into three levels for patients receiving invasive mechanical ventilation, achieving 89.08% accuracy. This model can be implemented to ventilators by edge computing, whose feasibility is approved.
Shuai Wang +6 more
wiley +1 more source
Investing in Primary Care to Reduce the Burden of Chronic Obstructive Pulmonary Disease. [PDF]
Yang T, Wu J, Chi C.
europepmc +1 more source
Mortality Patterns and Phenotypic Clusters in Trisomy 13: A Population‐Based Study From Japan
ABSTRACT Trisomy 13, the third most common autosomal trisomy after trisomy 21 and trisomy 18, is associated with a significantly high infant mortality rate. However, large‐scale studies examining causes of death in trisomy 13 remain scarce. Therefore, we aimed to better understand the mortality patterns.
Narumi Kato +2 more
wiley +1 more source
Correction: The PAR6B-PRKCI-PAR3 complex influences alveolar regeneration in patients with the emphysema subtype of chronic obstructive pulmonary disease. [PDF]
Wang D, Liu H, Bai S, Zheng X, Zhao L.
europepmc +1 more source
ABSTRACT Costello syndrome (CS) is a rare dominant HRAS RASopathy characterized by curly hair, cardiac abnormalities, craniofacial anomalies, and developmental delay. HRAS codon 58, 59, and 60 variants are associated with milder phenotypes. We describe a three‐generation family with a previously unreported heterozygous HRAS variant c.175G>A (p.Ala59Thr)
Nikole Rautiainen +10 more
wiley +1 more source
The Risk of Tuberculosis in Chronic Obstructive Pulmonary Disease Across Different Comorbidities. [PDF]
Liao KM, Kuo LT, Lu HY.
europepmc +1 more source
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim +9 more
wiley +1 more source
Integrating Bioinformatics Analysis with RT-qPCR Experimental Validation to Investigate Immune Cell and Telomere-Related Biomarkers in Chronic Obstructive Pulmonary Disease. [PDF]
Wang S, Tang W, Yang H.
europepmc +1 more source
Noninvasive ventilation for acute exacerbations of chronic obstructive pulmonary disease.
L. Aurent +24 more
semanticscholar +1 more source

