Results 31 to 40 of about 10,038,850 (263)

A computationally efficient non‐iterative four‐parameter sine fitting method

open access: yesIET Signal Processing, 2021
A computationally efficient four‐parameter least squares (LS) sine fitting method in the time domain is presented here. Unlike the most widespread procedure defined in the relevant IEEE standard, the proposed fitting is non‐iterative. This is achieved by
Balázs Renczes, Vilmos Pálfi
doaj   +1 more source

Evaluation of Dried Plasma Spot‐Based Quantification of Glial Fibrillary Acidic Protein as a Disease‐Associated Biomarker in Neuromyelitis Optica Spectrum Disorder

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To evaluate the diagnostic accuracy of glial fibrillary acidic protein (GFAP) measured in dried plasma spots versus conventional plasma‐ and serum‐GFAP testing for assessment of disease severity in aquaporin‐4 immunoglobulin G–positive neuromyelitis optica spectrum disorder (AQP4‐IgG+ NMOSD).
Felix Wohlrab   +19 more
wiley   +1 more source

Social risk factors in patients with cystic fibrosis: impacts on exacerbations, lung function, and BMI

open access: yesTherapeutic Advances in Respiratory Disease
Background: Cystic fibrosis (CF) outcomes are influenced by a myriad of genetic, microbiological, and environmental factors, as well as socioeconomic constraints. Studies have shown that low socioeconomic status is associated with a higher risk of death,
Zhuoyi Galvin Li   +11 more
doaj   +1 more source

Morbidity and treatment costs of cystic fibrosis in a middle-income country

open access: yesSingapore Medical Journal
Introduction: Asian children with cystic fibrosis (CF) managed in Malaysia have significant morbidity with limited access to life-sustaining treatments. We determined the morbidity and treatment cost of CF in a resource-limited country.
Shih Ying Hng, MMed (Paeds)   +14 more
doaj   +1 more source

Optimizing CFTR modulator therapy management for cystic fibrosis through the ReX platform

open access: yesFrontiers in Pediatrics, 2023
BackgroundCystic fibrosis (CF) is a chronic multi-systemic disease that requires a complex daily treatment regimen. Therefore, there is sub-optimal adherence to CF therapies, and it was shown to impact its clinical and economic burden.
Karin Yaacoby-Bianu   +9 more
doaj   +1 more source

Practical guidelines: lung transplantation in patients with cystic fibrosis [PDF]

open access: yes, 2014
There are no European recommendations on issues specifically related to lung transplantation (LTX) in cystic fibrosis (CF). The main goal of this paper is to provide CF care team members with clinically relevant CF-specific information on all aspects of ...
Wagner, T. O F   +46 more
core   +1 more source

xarray-contrib/cf-xarray:

open access: yes, 2021
a lightweight accessor for xarray objects that interprets CF ...
Shubhendra Singh Chauhan   +7 more
core   +1 more source

Molecular Diagnosis in Children With Febrile Seizures: Beyond the Conventional Clinical Classification

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Febrile seizures (FS) are currently classified as simple or complex primarily to describe seizure characteristics, with limited ability to identify the underlying etiology. We evaluated whether molecular diagnosis could complement conventional classification and improve the diagnosis and management of FS.
Jia Wang   +22 more
wiley   +1 more source

The WE-RISE™ multi-domain intervention: a feasibility study for the potential reversal of cognitive frailty in Malaysian older persons of lower socioeconomic status

open access: yesBMC Geriatrics
Background Cognitive frailty (CF) is an emerging concern among older persons, particularly within lower socioeconomic statuses (SES) populations. Currently, there is limited evidence on the potential reversibility of CF through multi-domain interventions
Resshaya Roobini Murukesu   +5 more
doaj   +1 more source

Colistimethate sodium powder and tobramycin powder for inhalation for the treatment of chronic Pseudomonas aeruginosa lung infection in cystic fibrosis: systematic review and economic model

open access: yesHealth Technology Assessment, 2013
Background: Cystic fibrosis (CF) is an inherited condition characterised by the abnormal transport of chloride ions across transporting epithelia.
P Tappenden   +5 more
doaj   +1 more source

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