Results 151 to 160 of about 390,338 (298)

Strategies to reduce diagnostic errors: A systematic review

open access: yes, 2019
Strategies to reduce diagnostic errors: A systematic ...
M Firipis (14466411)   +5 more
core  

Toward Safer Diagnoses: A SEIPS-Based Narrative Review of Diagnostic Errors. [PDF]

open access: yesDiagnostics (Basel)
Yen C   +3 more
europepmc   +1 more source

Effectiveness of rTMS on Working Memory and Inhibitory Impairments in Patients With Post‐Stroke Executive Deficits

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Considerable efforts have been dedicated to developing effective treatments for post‐stroke executive impairment (PSEI), among which repetitive transcranial magnetic stimulation (rTMS) has shown great potential. This study aimed to investigate the therapeutic effects of high‐frequency rTMS on working memory (WM) and response ...
Mengting Lao   +6 more
wiley   +1 more source

Diagnostic errors in clinical laboratory testing process: incidence and impacts on patient safety-a 3-year voluntary incident report analysis. [PDF]

open access: yesInt J Qual Health Care
Saengpattrachai M   +7 more
europepmc   +1 more source

GAD65 Antibody ELISA With Extended Reportable Range: Validation and Guidance for Neurological Practice

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To (1) validate GAD65‐ELISA detection and quantification for type 1 diabetes mellitus and autoimmune neurological diagnoses, (2) correlate ELISA results (reference range < 5 IU/mL) with established radioimmunoprecipitation assay (RIA; ≤ 0.02 nmol/L), and (3) define ELISA clinical utility and pitfalls.
Andrew McKeon   +11 more
wiley   +1 more source

Systemic analysis and modelling of diagnostic errors in medicine

open access: yes
Diagnostic accuracy is an important index of the quality of health care service. Missed, wrong or delayed diagnosis has a direct effect on patient safety.
Guo, Shijing
core  

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu   +21 more
wiley   +1 more source

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