Results 231 to 240 of about 1,120,551 (376)

A saliency-based search mechanism for overt and covert shifts of visual attention

, 2000
L. Itti, Christof Koch
openalex   +1 more source

Edges: saliency measures and automatic thresholding [PDF]

, 2002
Paul L. Rosin
openalex   +1 more source

JACMP 2025–2029 and beyond

Journal of Applied Clinical Medical Physics, EarlyView.
Michael Mills
wiley   +1 more source

Sensorless Salient-Pole PM Synchronous Motor Drives in All Speed Ranges

, 2000
Takaharu Takeshita, Akira Usui, Nobuyuki Matsui   +2 more
openalex   +2 more sources

Relationship of cognitive decline with glucocerebrosidase activity and amyloid‐beta 42 in DLB and PD

Annals of Clinical and Translational Neurology, EarlyView.
Abstract Objective Dementia with Lewy bodies (DLB) and Parkinson's disease (PD) share clinical, pathological, and genetic risk factors, including GBA1 and APOEε4 mutations. Biomarkers associated with the pathways of these mutations, such as glucocerebrosidase enzyme (GCase) activity and amyloid‐beta 42 (Aβ42) levels, may hold potential as predictive ...
Maria Camila Gonzalez, Linn Oftedal, Johannes Lange, Diego Alejandro Tovar‐Rios, Ole‐Bjørn Tysnes, Claire Paquet, Marta Marquié, Mercè Boada, Daniel Alcolea, Konrad Rejdak, Ewa Papuc, Jakub Hort, Cristian Falup‐Pecurariu, Dag Aarsland, Guido Alves, Jodi Maple‐Grødem   +15 more
wiley   +1 more source

Ready or Not, Here We Come: A Qualitative Study of the Transition From Graduate Medical Education to Independent Practice. [PDF]

J Grad Med Educ
Diemer G, Kuchera T, Zavodnick J, Frasso R, Jaffe R.   +4 more
europepmc   +1 more source

Progressive Myoclonus Epilepsy: Distinctive MRI Changes in Cerebellar and Motor Networks

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Progressive myoclonus epilepsy (PME) is a rare generalized epilepsy syndrome with a well‐characterized genetic basis. The brain networks that are affected to give rise to the distinctive symptoms of PME are less well understood. Methods Eleven individuals with PME with a confirmed genetic diagnosis and 22 controls were studied.
Jillian M. Cameron, Remika Mito, Samuel F. Berkovic, Graeme D. Jackson   +3 more
wiley   +1 more source

Retina-Inspired Models Enhance Visual Saliency Prediction. [PDF]

Entropy (Basel)
Shen G, Ma W, Zhai W, Lv X, Chen G, Tian Y.   +5 more
europepmc   +1 more source

Saliency-based multifoveated MPEG compression [PDF]

, 2003
Nitin Dhavale, Laurent Itti
openalex   +1 more source

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

Annals 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, Rhiana Schafer, Ashlin R. K. Roy, Andrzej Sokolowski, Noah G. Cryns, Dana Leichter, Argentina Lario Lago, Eliana Marisa Ramos, Yann Cobigo, Salvatore Spina, Lea T. Grinberg, Daniel H. Geschwind, Maria L. Gorno‐Tempini, Joel H. Kramer, Howard J. Rosen, Bruce L. Miller, William W. Seeley, David C. Perry   +17 more
wiley   +1 more source