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Neuronal intranuclear inclusion disease with mental abnormality: a case report
BackgroundNeuronal intranuclear inclusion disease (NIID) is a chronic progressive neurodegenerative disease that is characterized by the discovery of...
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Novel Mutations in CDC20 Are Associated with Female Infertility Due to Oocyte Maturation Abnormality and Early Embryonic Arrest
The cell division cycle 20 (CDC20) protein is a co-activator of anaphase-promoting complex/cyclosome (APC/C), required for mitotic exit and also...
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Automated identification of chest radiographs with referable abnormality with deep learning: need for recalibration
ObjectivesTo evaluate the calibration of a deep learning (DL) model in a diagnostic cohort and to improve model’s calibration through recalibration...
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Artificial intelligence system for identification of false-negative interpretations in chest radiographs
ObjectivesTo investigate the efficacy of an artificial intelligence (AI) system for the identification of false negatives in chest radiographs that...
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Persistent or recurrent Barrett’s neoplasia after an endoscopic therapy session is associated with DNA content abnormality and can be detected by DNA flow cytometric analysis of paraffin-embedded tissue
Endoscopic therapy is currently the standard of care for the treatment of high-grade dysplasia (HGD) or intramucosal adenocarcinoma (IMC) in patients...
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A transformer-based multi-task deep learning model for simultaneous infiltrated brain area identification and segmentation of gliomas
BackgroundThe anatomical infiltrated brain area and the boundaries of gliomas have a significant impact on clinical decision making and available...
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Automated identification of uncertain cases in deep learning-based classification of dopamine transporter SPECT to improve clinical utility and acceptance
PurposeDeep convolutional neural networks (CNN) are promising for automatic classification of dopamine transporter (DAT)-SPECT images. Reporting the...
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Identification of sudden cardiac death from human blood using ATR-FTIR spectroscopy and machine learning
ObjectiveThe aim of this study is to identify a rapid, sensitive, and non-destructive auxiliary approach for postmortem diagnosis of SCD, addressing...
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Timeliness of Early Identification and Referral of Infants with Social and Environmental Risks
The Early Intervention Parenting Partnerships (EIPP) program is a home visiting program that provides home visits, group services, assessments and...
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Improved identification of tumors in 18F-FDG-PET examination by normalizing the standard uptake in the liver based on blood test data
PurposeStandardized uptake values (SUVs) derived from 18 F-fluoro-2-deoxy-D-glucose positron emission tomography/computed tomography are a crucial...
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Enhancing Ophthalmic Triage: identification of new clinical features to support healthcare professionals in triage
ObjectiveTo investigate which features from a patient’s history are either high or low risk that could support healthcare professionals in ophthalmic...
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Identification and validation of senescence-related genes in polycystic ovary syndrome
BackgroundPolycystic ovary syndrome (PCOS) is an exceedingly intractable issue affecting female endocrine and reproductive health. However, the...
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Identification and Analysis of Atrial-Bronchial-Abdominal Disharmony in Patients with Isomeric Atrial Appendages
Ideally, the morphology of atrial appendages should solely be used to identify and differentiate patients with isomeric right and left atrial...
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Long-range and real-time PCR identification of a large SERPINC1 deletion in a patient with antithrombin deficiency
Congenital antithrombin (AT) or serpin C1 deficiency, caused by a SERPINC1 abnormality, is a high-risk factor for venous thrombosis. SERPINC1 is...
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Deconstructing emotion regulation in schizophrenia: the nature and consequences of abnormalities at the identification stage
Existing evidence suggests that emotion regulation is abnormal in schizophrenia and associated with undesirable clinical outcomes. However, this...
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Identification of neurological complications in childhood influenza: a random forest model
BackgroundAmong the neurological complications of influenza in children, the most severe is acute necrotizing encephalopathy (ANE), with a high...
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Multispectral Imaging Method for Rapid Identification and Analysis of Paraffin-Embedded Pathological Tissues
The study of the interaction between light and biological tissue is of great help in the identification of diseases as well as structural alterations...
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Identification and functional characterization of compound heterozygous CYP11B1 gene mutations
Purpose11β-Hydroxylase deficiency (11β-OHD) is the second leading cause of congenital adrenal hyperplasia (CAH), a rare autosomal recessive disease...
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Identification of a novel pyroptosis-related gene signature in human spermatogenic dysfunction
PurposeTo reveal the underlying roles that pyroptosis-related genes (PRGs) played in human spermatogenic dysfunction.
MethodsOne discovery set and...
