Results 171 to 180 of about 1,046,440 (397)

Prevalence of Cystic Fibrosis Carrier Status in Chronic Rhinosinusitis Without Nasal Polyp

International Forum of Allergy &Rhinology, EarlyView.
Do‐Yeon Cho, Adam J. Skelton, Jessica W. Grayson, Justin H. Turner, Bradford A. Woodworth   +4 more
wiley   +1 more source

Liver organoids: From 3D printing to biomedical applications

BMEMat, EarlyView.
A comprehensive review on liver organoids culture techniques from 3D printing to organ‐on‐chip, as well as focusing on challenges and perspectives for advancement liver organoids in various future applications. Abstract The liver is an immune organ, especially an immune tolerance organ.
Ying Shi, Xin Han, Zheng Zhang, Jiangtao Xu, Guozhen Liu   +4 more
wiley   +1 more source

Spring‐infusors: How a simple and small solution can create king‐sized complexity

Nursing Open, Volume 10, Issue 2, Page 1125-1134, February 2023., 2023
Abstract Aim The aims of the study were to investigate family and hospital staff views about the use of spring‐infusor devices for administration of intravenous antibiotic medications, to examine if the device is acceptable and feasible and to map a process for implementation.
Pamela Laird, Charlotte Burr, Fenella J. Gill, André Schultz   +3 more
wiley   +1 more source

Eradication of Burkholderia cepacia Using Inhaled Aztreonam Lysine in Two Patients with Bronchiectasis

Case Reports in Pulmonology, 2014
There are not many articles about the chronic bronchial infection/colonization in patients with underlying lung disease other than cystic fibrosis (CF), especially with non-CF bronchiectasis (NCFBQ). The prevalence of B. cepacia complex is not well known
A. Iglesias, I. Artiles, J. J. Cabanillas, R. Álvarez-Sala, C. Prados   +4 more
doaj   +1 more source

Bayesian Model Averaging for the X-Chromosome Inactivation Dilemma in Genetic Association Study [PDF]

arXiv, 2017
X-chromosome is often excluded from the so called `whole-genome' association studies due to its intrinsic difference between males and females. One particular analytical challenge is the unknown status of X-inactivation, where one of the two X-chromosome variants in females may be randomly selected to be silenced.
arxiv  

Side-effects to antibiotics in cystic fibrosis: dental changes in relation to antibiotic administration. [PDF]

, 1967
J.N. Swallow, Jordan D. Haller, William F. Young   +2 more
openalex   +1 more source

Cystic fibrosis lung environment and Pseudomonas aeruginosa infection

BMC Pulmonary Medicine, 2016
BackgroundThe airways of patients with cystic fibrosis (CF) are highly complex, subject to various environmental conditions as well as a distinct microbiota.
Anjali Y Bhagirath, Yanqi Li, Deepti Somayajula, M. Dadashi, Sara Badr, K. Duan   +5 more
semanticscholar   +1 more source

Detection of cytokines in nasal lavage samples of patients with cystic fibrosis: comparison of two different cytokine detection assays

BMC Pulmonary Medicine
Background Cystic fibrosis (CF) is a genetic multisystem disorder. Inflammatory processes, which presumably begin early in infancy, play a crucial role in the progression of the disease. The detection of inflammatory biomarkers, especially in the airways,
Teresa Fuchs, Manuela Zlamy, Thomas Zöggeler, Dorothea Appelt, Katharina Niedermayr, Anja Siedl, Verena Gasser, Johannes Eder, Helmut Ellemunter   +8 more
doaj   +1 more source

Sparse Meets Dense: A Hybrid Approach to Enhance Scientific Document Retrieval [PDF]

arXiv
Traditional information retrieval is based on sparse bag-of-words vector representations of documents and queries. More recent deep-learning approaches have used dense embeddings learned using a transformer-based large language model. We show that on a classic benchmark on scientific document retrieval in the medical domain of cystic fibrosis, that ...
arxiv  

N.A.C. and Antibiotics in Cystic Fibrosis [PDF]

, 1965
David H. Lawson, B. A. Saggers
openalex   +1 more source