Results 181 to 190 of about 3,655,523 (362)

Evolutionary Optimization Techniques on Computational Grids [PDF]

open access: bronze, 2002
Baker Abdalhaq   +3 more
openalex   +1 more source

Theory and Applications of Evolutionary Computation

open access: yesApplied Computational Intelligence and Soft Computing, 2010
Tzung-Pei Hong   +2 more
doaj   +1 more source

Integrating evolutionary computation with neural networks [PDF]

open access: green, 2002
E. Vonk   +3 more
openalex   +1 more source

System Identification for Structure-Unknown Linear Dynamical System by Evolutionary Computation

open access: bronze, 2000
Toshiro Kumon   +5 more
openalex   +2 more sources

The burden of intracranial atherosclerosis on cerebral small vessel disease: A community cohort study

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
Abstract Objective Exploring the prevalence and association between intracranial atherosclerosis (ICAS) and cerebral small vessel diseases (CSVD), this study delved beyond the current scope, utilising high‐resolution vessel wall MRI (HRVW‐MRI) to investigate how subtle changes in intracranial atherosclerotic features influence the various burdens of ...
Joseph Amihere Ackah   +6 more
wiley   +1 more source

Reducing Time of Evolutionary Computation using Fitness Estimation

open access: bronze, 2000
Yasushi Hankai   +2 more
openalex   +2 more sources

Clinical and Imaging Features of Sporadic and Genetic Frontotemporal Lobar Degeneration TDP‐43 A and B

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Certain frontotemporal lobar degeneration subtypes, including TDP‐A and B, can either occur sporadically or in association with specific genetic mutations. It is uncertain whether syndromic or imaging features previously associated with these patient groups are subtype or genotype specific.
Sean Coulborn   +17 more
wiley   +1 more source

Cerebello‐Prefrontal Connectivity Underlying Cognitive Dysfunction in Spinocerebellar Ataxia Type 2

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Spinocerebellar ataxia type 2 (SCA2) is a hereditary cerebellar degenerative disorder, with motor and cognitive symptoms. The constellation of cognitive symptoms due to cerebellar degeneration is named cerebellar cognitive affective syndrome (CCAS), which has increasingly been recognized to profoundly impact patients' quality of life;
Ami Kumar   +7 more
wiley   +1 more source

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