Results 161 to 170 of about 238,742 (294)

Explainable AI‐Driven Optimization of Electrode Activation Reduces Power Consumption While Preserving Object Recognition in Retinal Prostheses

Advanced Intelligent Systems, EarlyView.
Explainable artificial intelligence (XAI) guides selective electrode activation in retinal prostheses by emphasizing visually informative regions. XAI‐assisted phosphene generation maintains object recognition performance while significantly reducing stimulation power.
Sein Kim, Hamin Shim, Maesoon Im
wiley   +1 more source

An improved neighbourhood-based contrast limited adaptive histogram equalization method for contrast enhancement on retinal images. [PDF]

Int J Ophthalmol
Arulraj A, Mariadhason JS, Ronjalis RR.
europepmc   +1 more source

Dilated residual FPN-based segmentation for mouse retinal images. [PDF]

Heliyon, 2023
Che Z, Bi F, Sun Y, Xing W, Huang H, Zhang X.   +5 more
europepmc   +1 more source

AI‐Assisted IoT‐Enabled ECG Monitoring: Integrating Foundational and Generative AI Tools for Sustainable Smart Healthcare—Recent Trends

AI &Innovation, EarlyView.
ABSTRACT The rapid evolution of the Internet of Things (IoT) has significantly advanced the field of electrocardiogram (ECG) monitoring, enabling real‐time, remote, and patient‐centric cardiac care. This paper presents a comprehensive survey of AI assisted IoT‐based ECG monitoring systems, focusing on the integration of emerging technologies such as ...
Amrita Choudhury, Kandarpa Kumar Sarma, Lachit Dutta   +2 more
wiley   +1 more source

Optimizing retinal images based carotid atherosclerosis prediction with explainable foundation models. [PDF]

NPJ Digit Med
Lee H, Kim J, Kwak S, Rehman A, Park SM, Chang J.   +5 more
europepmc   +1 more source

Swallowing and Communication in Cockayne Syndrome: Clinical Characteristics and Management

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cockayne syndrome (CS) is an ultrarare genetic disorder associated with genes encoding proteins involved in DNA repair. The clinical course of CS involves neurodevelopmental and neurodegenerative features, including swallowing and communication impairments.
Abigail M. Spoden, Katlyn E. McGrattan, Peter B. Kang   +2 more
wiley   +1 more source

A novel approach for the segmentation of retinal images by integration K-means clustering algorithm with graph cut for image segmentation. [PDF]

Sci Rep
Bhoopalan R, Priyadharshini S.
europepmc   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12‐Related Developmental Disorders

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

A deep learning system for detecting systemic lupus erythematosus from retinal images. [PDF]

Cell Rep Med
Li T, Lin S, Guan Z, Zhou Y, Zeng D, Wang Z, Zhou Y, Fang P, Yu S, Liu R, Chen X, Wang YJ, Lu Y, Shu J, Qin Y, Wu Y, Wu Y, Wu C, Zhang S, Shen J, Li H, Chen T, Li J, Tham YC, Sabanayagam C, Zheng YF, Wagner SK, Keane PA, Wong TY, Dai R, Sheng B.   +30 more
europepmc   +1 more source

Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet, Sylvie A. Adams, Zoe S. Katz, Christal G. Delagrammatikas, Kosuke Izumi, Winifred Sigal, Kim Ventarola, Elaine H. Zackai, Julia E. Reid, Grant T. Liu, Jennifer M. Kalish   +10 more
wiley   +1 more source