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We proposed a framework to detect the video contents of depressed and non-depressed subjects. First we characterized the expressed emotions in the video stream using Gabor wavelet features extracted at the facial landmarks which were detected using landmark model matching algorithm. Depressed and non-depressed class models were constructed using Gaussian(More)
Research has identified anger as prominent in, and an influence on, treatment outcome for military veterans with posttraumatic stress disorder (PTSD). This study examined factors influencing the relationship between anger and outcome to improve treatment effectiveness. Participants comprised 103 veterans attending PTSD treatment. Measures of PTSD and(More)
STUDY OBJECTIVES The intent of the study was to explore the nature and function of the cardiovascular activation response that occurs at an arousal from sleep. DESIGN Four experiments were conducted. The first compared the pattern of physiologic response to orienting and startle stimuli and arousal from sleep. The second and third measured the amplitude(More)
The predominant work in static program analysis is focused on whole program analysis assuming that the whole program is present at analysis time and the only unknowns are program inputs. However, for library designers it is of paramount importance to perform semantic checks via static program analysis tools without the presence of an application. The(More)
This study sought to examine the impact of personality factors on symptom change following treatment for 141 Vietnam veterans with chronic combat-related posttraumatic stress disorder (PTSD) using the Minnesota Multiphasic Personality Inventory-2 (Butcher, Dahlstrom, Graham, Tellegen, & Kaemmer, 1989). A series of partial correlation and linear multivariate(More)
  • Heon Yung Gee, Carolin E. Sadowski, Pardeep K. Aggarwal, Jonathan D. Porath, Toma A. Yakulov, Markus Schueler +36 others
  • 2016
Steroid-resistant nephrotic syndrome (SRNS) causes 15% of chronic kidney disease (CKD). Here we show that recessive mutations in FAT1 cause a distinct renal disease entity in four families with a combination of SRNS, tubular ectasia, haematuria and facultative neurological involvement. Loss of FAT1 results in decreased cell adhesion and migration in(More)
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