Results 221 to 230 of about 1,771,429 (303)

On the impact of mass screening for SARS-CoV-2 through self-testing in Greece. [PDF]

open access: yesFront Public Health
Gilmour S   +5 more
europepmc   +1 more source

Interleukin‐6 as a Key Biomarker in Facioscapulohumeral Dystrophy: Evidence From Longitudinal Analyses

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a progressive neuromuscular disorder with no approved treatments. Identifying reliable biomarkers is critical to monitor disease severity, activity, and progression. Interleukin‐6 (IL‐6) has been proposed as a candidate biomarker, but longitudinal validation is limited ...
Jonathan Pini   +13 more
wiley   +1 more source

Cystic renal mass screening: machine-learning-based radiomics on unenhanced computed tomography [PDF]

open access: yesDiagn Interv Radiol
Huang L   +8 more
europepmc   +1 more source

Yield, Efficiency, and Costs of Mass Screening Algorithms for Tuberculosis in Brazilian Prisons. [PDF]

open access: yesClin Infect Dis, 2021
Santos ADS   +10 more
europepmc   +1 more source

Retrospective study of sputum cytology in primary adenocarcinoma of the lung detected by chest X-ray film in population-based mass screening.

open access: diamond, 1998
Maya SASAKI   +9 more
openalex   +2 more sources

A High-Throughput Mass Spectrometry Assay Coupled with Redox Activity Testing Reduces Artifacts and False Positives in Lysine Demethylase Screening [PDF]

open access: hybrid, 2015
Tim J. Wigle   +11 more
openalex   +1 more source

Additional file 5 of The NORMAN Suspect List Exchange (NORMAN-SLE): facilitating European and worldwide collaboration on suspect screening in high resolution mass spectrometry

open access: gold, 2022
Hiba Mohammed Taha   +96 more
openalex   +1 more source

SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas   +18 more
wiley   +1 more source

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