Results 51 to 60 of about 90,840 (284)
Frontal fibrosing alopecia and lichen planus pigmentosus: diagnosis and therapeutic challenge [PDF]
Anais Brasileiros de Dermatologia, 2017 Frontal fibrosing alopecia is a variant of lichen planopilaris with marginal progressive hair loss on the scalp, eyebrows and axillae. We report a case of frontal fibrosing alopecia and lichen planus pigmentosus in a postmenopausal woman, that started ...
Fabiane Andrade Mulinari-Brenner +3 more
doaj +2 more sources
Using data visualization to deduce faces expressions [PDF]
, 2018 Conferência Internacional, realizada na Turquia, de 6-8 de setembro de 2018.Collect and examine in real time multi modal sensor data of a human face, is an important problem in computer vision, with applications in medical and monitoring analysis ...
Brito, Paulo, Carvalho, Elizabeth
core
Decoding Emotional Signatures of Ethical Ads: An Analysis of Actor‐Viewer Synchrony
Journal of Consumer Behaviour, EarlyView.ABSTRACT We examine whether ethical advertisements differ from conventional ads in their on‐screen emotional signatures and whether those signatures transfer to actor‐viewer synchrony. Study 1 analyses 138 professionally produced YouTube ads using Automated Facial Expression Recognition (AFER) and Convolutional Neural Networks (CNN) to quantify actor ...
Vik Naidoo, Nicolas Hamelin
wiley +1 more source
Speaker Eyebrow Raises in the Transition Space
Social InteractionIn this article, we examine a distinctive multimodal phenomenon: a participant, gazing at a recipient, raising both eyebrows upon the completion of their own turn at talk – that is, in the transition space between turns at talk (Sacks, Schegloff and ...
Rebecca Clift, Giovanni Rossi
doaj +1 more source
Simbiosis: Journal of Biological Sciences, 2017 This study was conducted to find out the determinant allele frequencies and variations of characteristics of face and earlobe, based on the presence or absence of attached earlobes, connected eyebrows (unibrow), dimples, and tongue-rolling on Subaya ...
Yulia Mirayanti +2 more
doaj +1 more source
Vogt-Koyanagi-Harada Syndrome in a 10 Years Old Child [PDF]
, 2011 The Vogt-Koyanagi-Harada (VKH) syndrome is a rare systemic disorder of uveitis, dysacousia, vitiligo, premature graying of the hair, eyebrows and eyelashes, and meningoencephalitis. Although frequently unrecognised,VKH may affect children.
Singh, T, Sufi, AR, Zargar, S
core +1 more source
Compound Heterozygosity in PGAP3 Causing Mabry Syndrome in a South African Patient
American Journal of Medical Genetics Part A, EarlyView.
Carli Loubser, Shahida Moosa
wiley +1 more source
Developmental Dynamics, EarlyView.Abstract Trichorhinophalangeal syndrome (TRPS) is a rare genetic disease inherited in an autosomal dominant manner. It occurs in 1 in 100,000 people globally and is caused by several types of mutations of the TRPS1 gene. Since the first human patient was reported in 1966, typical and atypical pathologies, disease courses, and treatment case ...
Naoya Saeki +6 more
wiley +1 more source
Attribute-Guided Face Generation Using Conditional CycleGAN
, 2018 We are interested in attribute-guided face generation: given a low-res face input image, an attribute vector that can be extracted from a high-res image (attribute image), our new method generates a high-res face image for the low-res input that ...
Lu, Yongyi +2 more
core +2 more sources
Developmental Dynamics, EarlyView.Abstract Background Integrin is an αβ heterodimeric receptor to the extracellular matrix; its binding to the matrix recruits focal adhesions to two NPxY motifs, the tyrosine phosphorylation sites in the cytoplasmic domain. Studies found that replacing tyrosines (Y) with phenylalanines (F) in the motif of β1 integrin displayed little developmental or ...
Josh Haram Bumm +7 more
wiley +1 more source