Results 81 to 90 of about 212,640 (241)

Artificial Intelligence in Ophthalmology: From Methodological Advances to Clinical Translation and Future Directions

open access: yesEye &ENT Research, EarlyView.
ABSTRACT Artificial intelligence (AI) is reshaping ophthalmology from task‐specific image analysis toward multimodal, longitudinal, and clinically integrated decision support. This narrative review summarizes the methodological evolution of ophthalmic AI, including traditional machine learning, task‐specific deep learning, self‐supervised learning ...
Yuxin Liu, Hanruo Liu
wiley   +1 more source

The Positive Career Goal Discrepancy Scale: Development and Initial Validation

open access: yes, 2020
The 15-item Positive Career Goal Discrepancy Scale was developed to assess emerging adults’ appraisals of the extent to which their current career progress exceeds their set career goals.
Akmal, Sari Z   +3 more
core   +1 more source

Establishing consensus diagnostic criteria for ring chromosome 20 syndrome: A modified electronic Delphi consensus study

open access: yesEpilepsia, EarlyView.
Abstract Objective This study was undertaken to establish expert consensus clinical and diagnostic criteria for ring chromosome 20 syndrome using a modified electronic Delphi process. Methods In this modified two‐round electronic Delphi consensus study, international experts rated candidate statements using a 9‐point Likert scale.
Abizairie Sánchez‐Feliciano   +15 more
wiley   +1 more source

A discrepancy principle for Poisson data: uniqueness of the solution for 2D and 3D data [PDF]

open access: yes, 2010
This paper is concerned with the uniqueness of the solution of a nonlinear equation, named discrepancy equation. For the restoration problem of data corrupted by Poisson noise, we have to minimize an objective function that combines a data-fidelity ...
Ruggiero, Valeria, Bonettini, Silvia
core  

Translocation (8;21) in acute nonlymphocytic leukemia delineated by chromosomal in situ suppression hybridization [PDF]

open access: yes, 1991
In situ suppression hybridization with recombinant bacteriophage DNA libraries for chromosomes 8 and 21 was performed in two cases of acute nonlymphocytic leukemia, type FAB M2.
Cremer, Thomas   +5 more
core   +1 more source

Discrepancy Minimization via Regularization

open access: yes, 2023
appears in SODA 2023International audienceWe introduce a new algorithmic framework for discrepancy minimization based on regularization. We demonstrate how varying the regularizer allows us to re-interpret several breakthrough works in algorithmic ...
Vladu, Adrian, Pesenti, Lucas
core   +1 more source

Comparative assessment of artificial intelligence chatbots' performance in responding to healthcare professionals' and caregivers' questions about Dravet syndrome

open access: yesEpilepsia Open, EarlyView.
Abstract Objective Artificial intelligence chatbots have been a game changer in healthcare, providing immediate, round‐the‐clock assistance. However, their accuracy across specific medical domains remains under‐evaluated. Dravet syndrome remains one of the most challenging epileptic encephalopathies, with new data continuously emerging in the ...
Joana Jesus‐Ribeiro   +4 more
wiley   +1 more source

Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2015
Objective: To present prenatal diagnosis of mosaic trisomy 15 at amniocentesis. Materials and methods: A 37-year-old woman underwent amniocentesis at 17 weeks of gestation because of advanced maternal age.
Chih-Ping Chen   +6 more
doaj   +1 more source

An Examination of the Statistical Discrepancy and Private Investment Expenditure [PDF]

open access: yes
The statistical discrepancy is often used to gauge the reliability of national accounts data. Particularly since the mid-1980’s the statistical discrepancy in Australia has grown significantly in size and variance.
Christopher Bajada
core  

Genetic epilepsies with myoclonic seizures: Mechanisms and syndromes

open access: yesEpilepsia Open, EarlyView.
Abstract Genetic epilepsy with myoclonic seizures encompasses a heterogeneous spectrum of conditions, ranging from benign and self‐limiting forms to severe, progressive disorders. While their causes are diverse, a significant proportion stems from genetic abnormalities.
Antonietta Coppola   +3 more
wiley   +1 more source

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