Results 71 to 80 of about 1,451,836 (324)

Measuring fibrinolysis: from research to routine diagnostic assays

open access: yesJournal of Thrombosis and Haemostasis, 2018
Development and standardization of fibrinolysis methods have progressed more slowly than coagulation testing and routine high‐throughput screening tests for fibrinolysis are still lacking. In laboratory research, a variety of approaches are available and
C. Longstaff
semanticscholar   +1 more source

Potential Early Risk Biomarkers for Reduced Forced Expiratory Volume in Children Post‐Hematopoietic Cell Transplantation

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT We sought to identify potential early risk biomarkers for lung disease in children post‐allogeneic HCT. Patients with pulmonary function tests 3 months post‐transplant and plasma samples between days 7 and 14 post‐HCT were included. Six of 27 subjects enrolled had reduced forced expiratory volume 1 (FEV1) z scores.
Isabella S. Small   +3 more
wiley   +1 more source

Investigating rapid diagnostic testing in Kenya’s health system, 2018–2020: validating non-reporting in routine data using a health facility service assessment survey

open access: yesBMC Health Services Research, 2023
Background Understanding the availability of rapid diagnostic tests (RDTs) is essential for attaining universal health care and reducing health inequalities.
Angela K Moturi   +4 more
doaj   +1 more source

Decision Support Systems For Disease Control in Winter Wheat. [PDF]

open access: yes, 2001
End of Project ReportA leaf diagnostic test and a computer-based decision support system were evaluated for the control of diseases of winter wheat caused by Septoria spp.
Burke, J.J.   +2 more
core  

Psychosocial Outcomes in Patients With Endocrine Tumor Syndromes: A Systematic Review

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Introduction The combination of disease manifestations, the familial burden, and varying penetrance of endocrine tumor syndromes (ETSs) is unique. This review aimed to portray and summarize available data on psychosocial outcomes in patients with ETSs and explore gaps and opportunities for future research and care.
Daniël Zwerus   +6 more
wiley   +1 more source

Effectiveness of professional and patient-oriented strategies in reducing vitamin D and B12 test ordering in primary care: a cluster randomised intervention study

open access: yesBJGP Open, 2021
Background: Vitamin tests are increasingly ordered by GPs, but a clinical and evidence-based indication is often lacking. Harnessing technology (that is, decision support tools and redesigning request forms) have been shown to reduce vitamin requests ...
Saskia van Vugt   +5 more
doaj   +1 more source

Evaluation of the Performance of Five Diagnostic Tests for Fasciola hepatica Infection in Naturally Infected Cattle Using a Bayesian No Gold Standard Approach

open access: yesPLoS ONE, 2016
The clinical and economic importance of fasciolosis has been recognised for centuries, yet diagnostic tests available for cattle are far from perfect.
S. Mazeri   +4 more
semanticscholar   +1 more source

Nutritional and Behavioral Intervention for Long‐Term Childhood Acute Leukemia Survivors With Metabolic Syndrome

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Purpose Metabolic syndrome (MetS) is a common complication in survivors of childhood acute lymphoblastic and myeloid leukemia (AL), and a major risk factor for premature cardiovascular disease, type‐2‐diabetes, and metabolic dysfunction‐associated steatotic liver disease (MASLD).
Visentin Sandrine   +10 more
wiley   +1 more source

Novel electrodiagnostic provocative techniques for the diagnosis of suspected tarsal tunnel syndrome

open access: yesEgyptian Rheumatology and Rehabilitation, 2022
Background Electrodiagnostic tests  (EDXTs) have been considered the gold standard method for the diagnosis of tarsal tunnel syndrome (TTS); however, definitive tests has not yet been discovered.
Mona M. Hasab ElNaby   +2 more
doaj   +1 more source

Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies [PDF]

open access: yesGenome Medicine, 2019
Diagnosis of primary immunodeficiencies (PIDs) is complex and cumbersome yet important for the clinical management of the disease. Exome sequencing may provide a genetic diagnosis in a significant number of patients in a single genetic test.In May 2013, we implemented exome sequencing in routine diagnostics for patients suffering from PIDs.
Arts P   +51 more
openaire   +9 more sources

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