Problems in learning with hypertext systems have been claimed to be caused by high levels of disorientation and cognitive load. This was recognized by DeStefano and LeFevre [DeStefano, D., & LeFevre, J. -A., (2007). Cognitive load in hypertext reading: A review. Computers in Human Behavior, 23(3), 1616–1641.] who predicted an increase of cognitive load and impairment of learning for hypertexts ...

INCE the discovery by MULLER with Drosophila (1927) and by STADLER with barley (1928) that the frequency of visible and lethal mutations is greatly increased by X-irradiation, a wide variety of organisms has been subjected to X-ray treatment by different investigators to elucidate the nature of the induced genetic changes. Although it is generally accepted that the majority of these mutations a...

A recent paper by Lefevre et al. (2014) in PLoS One reported that individual differences in facial structure predicted assertiveness in brown capuchin monkeys (Sapajus spp). Specifically, variation in the facial width-to-height ratio (fWHR) was positively correlated with alpha status and a composite measure of assertiveness. This novel finding adds to a growing body of evidence indicating that ...

Danny Dvir, MD; John Webb, MD; Stephen Brecker, MD; Sabine Bleiziffer, MD; David Hildick-Smith, MD; Antonio Colombo, MD; Fleur Descoutures, MD; Christian Hengstenberg, MD; Neil E. Moat, FRCS; Raffi Bekeredjian, MD; Massimo Napodano, MD; Luca Testa, MD, PhD; Thierry Lefevre, MD; Victor Guetta, MD; Henrik Nissen, MD, PhD; José-Marı́a Hernández, MD; David Roy, MD; Rui C. Teles, MD; Amit Segev, MD; ...

HAL is a multi-disciplinary open access archive for the deposit and dissemination of scientific research documents, whether they are published or not. The documents may come from teaching and research institutions in France or abroad, or from public or private research centers. L’archive ouverte pluridisciplinaire HAL, est destinée au dépôt et à la diffusion de documents scientifiques de niveau...

The hereditary dentine disorders, dentinogenesis imperfecta (DGI) and dentine dysplasia (DD), comprise a group of autosomal dominant genetic conditions characterised by abnormal dentine structure affecting either the primary or both the primary and secondary dentitions. DGI is reported to have an incidence of 1 in 6,000 to 1 in 8,000, whereas that of DD type 1 is 1 in 100,000. Clinically, the t...

1:30pm 3:00pm APCCM 1 Keynote ACSC 2 Software Engineering and Formal Methods ACE 1 AUIC 1 Augmented Reality ADC 1a Invited Talk AusGRID 1 Logic and Refinement for Charts Greg Reeve, Steve Reeves Up Close and Pedagogical: Computing Academics Talk About Teaching C. Kutay, R. Lister Evaluation of User Satisfaction and Learnability for Outdoor Augmented Reality Gaming Benjamin Avery, Wayne Piekarsk...