Deep learning automatic segmentation and radiomics model for diagnosing pancreatic solid neoplasms in MRI. [PDF]
Shi YJ +7 more
europepmc +1 more source
Automated image detection and segmentation in blood smears [PDF]
Steven S.S. Poon +2 more
openalex +1 more source
ABSTRACT Background Mitofusin 2 (MFN2) is a major causative gene for axonal Charcot – Marie – Tooth disease type 2A (CMT2A), with a wide phenotypic spectrum. Comprehensive large ‐ scale genotype – phenotype association studies are essential for understanding disease pathogenesis and improved clinical management.
Masahiro Ando +13 more
wiley +1 more source
Convolutional neural network based system for fully automatic FLAIR MRI segmentation in multiple sclerosis diagnosis. [PDF]
Darestani AA +6 more
europepmc +1 more source
ABSTRACT Background Neurodegeneration with brain iron accumulation (NBIA) comprises a genetically and clinically heterogeneous group of rare neurological disorders characterized particularly by iron accumulation in the basal ganglia. To date, 15 genes have been associated with NBIA.
Seda Susgun +95 more
wiley +1 more source
Deep learning based retinal hard exudates quantification of optical coherence tomography. [PDF]
Yoon CK, Lee HW, Kim HW, Kim JL.
europepmc +1 more source
A Methodological Comment on "Economic Segmentation, Worker Power, and Income Inequality"
Donald Tomaskovic‐Devey +3 more
openalex +2 more sources
Decreased Serum 5‐HT: Clinical Correlates and Regulatory Role in NMJ of MG
ABSTRACT Objective Although 5‐Hydroxytryptamine (5‐HT) indirectly stimulates muscle contraction and participates in regulating Acetylcholine receptor (AChR) cluster homeostasis in cellular, animal, and clinical studies, evidence regarding its potential to modulate muscle contraction in myasthenia gravis (MG) remains limited.
Xinru Shen +18 more
wiley +1 more source
Research on Instance Segmentation Algorithm for Caged Chickens in Infrared Images Based on Improved Mask R-CNN. [PDF]
Chen Y +8 more
europepmc +1 more source
RAB39B Related Parkinsonism in an Italian Family: A Unique Use of Advanced Therapies
ABSTRACT Parkinson's disease (PD) is a neurodegenerative disorder that may sometimes be caused by deleterious genetic variants. Among them, RAB39B polymorphisms are known as rare causes of early‐onset PD associated with intellectual disability (Waisman's syndrome).
Caterina Del Regno +13 more
wiley +1 more source

