Results 81 to 90 of about 181,498 (377)

The Effect of Immersion Technology on the Quality of Life in Older Adults: A Systematic Review

AGING MEDICINE, EarlyView.
Immersive technologies, especially virtual reality (VR), significantly improve the quality of life for older adults by enhancing physical health, cognitive function, and psychological well‐being. These technologies can be adapted to meet individual needs, making them an effective tool for addressing the challenges of aging.
Solmaz Sohrabei, Vahideh Zolfaghari, Seyed Jafar Ehsanzadeh   +2 more
wiley   +1 more source

Population Health Solutions for Assessing Cognitive Impairment in Geriatric Patients. [PDF]

, 2018
In December 2017, the National Academy of Neuropsychology convened an interorganizational Summit on Population Health Solutions for Assessing Cognitive Impairment in Geriatric Patients in Denver, Colorado. The Summit brought together representatives of a
Adler, Deb, Alban, Christopher, Bondi, Mark, Braun, Michelle, Cagigas, Xavier, Daven, Morgan, Denney, Robert L, Drozdick, Lisa, Foster, Norman L, Golden, Tamara, Hwang, Ula, Iverson, Grant, Ivey, Laurie, Kramer, Joel, Lacritz, Laura, Lantz, Melinda, Latts, Lisa, Ling, Shari M, Malone, Michael, Maria Lopez, Ana, Martin-Plank, Lori, Maslow, Katie, McConnel, Charles E, Melady, Don, Messer, Melissa, Meyers, John, Most, Randi, Norris, Margaret P, Perry, William, Pliskin, Neil, Roebuck-Spencer, Tresa, Shafer, David, Silver, Cheryl, Silverberg, Nina, Thomas, Colin M, Thornhill, Laura, Tsai, Jean, Vakharia, Nirav, Waters, Martin   +38 more
core   +2 more sources

The Behavioral Phenotype and Importance of Multidisciplinary Care in Patients With Sotos Syndrome: A Single‐Center Experience

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Sotos syndrome is an autosomal dominant condition caused by pathogenic variants in the NSD1 gene on chromosome 5q35. It is characterized by macrosomia, distinctive facial features, and developmental delays. Patients are also reported to have a behavioral phenotype including autism spectrum disorder, attention deficit/hyperactivity disorder ...
Aravind Viswanathan, Andrew M. George, Evan R. Hathaway, Carlyn Glatts, Jennifer M. Kalish   +4 more
wiley   +1 more source

The neuropsychology of disgust [PDF]

Social Cognitive and Affective Neuroscience, 2013
Beginning with the landmark case of Phineas Gage (Harlow, 1868), studies of neurological patients with ventromedial prefrontal cortex (vmPFC) damage have time and again demonstrated a critical role for this brain area in various aspects of emotion, social cognition and decision-making.
openaire   +3 more sources

Which executive functioning deficits are associated with AD/HD, ODD/CD and comorbid AD/HD+ODD/CD? [PDF]

, 2005
Item does not contain fulltextThis study investigated (1) whether attention deficit/hyperactivity disorder (AD/HD) is associated with executive functioning (EF) deficits while controlling for oppositional defiant disorder/conduct disorder (ODD/CD), (2 ...
A. Angold, A. Ardila, A. B. Morgan, A. Baddeley, A. C. Kalff, A. Dagher, A. Kempton, A. L. Benton, A. M. Owen, A. Scheres, B. A. Shaywitz, B. Aronowitz, B. F. Pennington, C. A. Riccio, C. A. Riccio, C. Clark, C. D. Frith, C. J. Aman, D. Carlin, D. MacLeod, D. R. Lynam, D. R. Offord, E. A. Phelps, E. L. Hart, E. M. Mahone, E. M. Perugini, E. Miller, F. M. Crinella, F. X. Castellanos, F. X. Castellanos, G. Groth-Marnat, G. M. Grodzinsky, H. S. Levin, J. A. Sergeant, J. A. Sergeant, J. B. Rowe, J. Biederman, J. C. Haggerty, J. Cohen, J. Duncan, J. Oosterlaan, J. Oosterlaan, J. Oosterlaan, J. Oosterlaan, J. Oosterlaan, J. Pujol, J. R. Stroop, J. R. Séguin, J. R. Séguin, J. T. Nigg, J. T. Nigg, J. T. Nigg, J. Toupin, K. A. Lockwood, K. L. Shue, K. Rezai, L. J. Schuerholz, M. A. Lau, M. B. Denckla, M. C. Welsh, M. C. Welsh, M. D. Lezak, M. Déry, M. J. Cohen, M. J. Reader, M. L. Speltz, M. Petrides, M. Petrides, N. Chhabildas, P. J. Eslinger, P. M. J. Pollux, P. R. Giancola, P. R. Giancola, R. A. Barkley, R. A. Barkley, R. A. Barkley, R. A. Barkley, R. A. Barkley, R. Elliott, R. G. Morris, R. Klorman, R. Kooijmans, R. Krikorian, R. Loeber, R. Loeber, R. Loeber, R. Milich, R. Schachar, R. Schlosser, R. W. Parks, R. W. Wiers, S. C. Baker, S. Daigneault, S. Houghton, S. J. Archibald, S. V. Faraone, T. E. Moffitt, T. E. Moffitt, T. E. Moffitt, T. E. Moffitt, T. J. Power, T. M. Achenbach, T. M. Achenbach, T. Shallice, T. Shallice, T. Shallice, W. C. Culbertson, W. D. Gaillard, W. E. Pelham, W. E. Pelham   +109 more
core   +1 more source

The Multifaceted Etiology of Mental Disorders With a Focus on Trace Elements, a Review of Recent Literature

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Mental disorders are a significant global public health concern, affecting nearly one in eight individuals worldwide. This review investigates the multifaceted etiology of mental disorders—specifically major depressive disorder (MDD), schizophrenia (SCZ), and bipolar disorder (BD)—through genetic, neurobiological, and environmental ...
Maria Francesca Astorino, Marco Calabrò, Carmenrita Infortuna, Maria Rosaria Anna Muscatello, Silvana Briuglia, Nicola Cicero, Chiara Fabbri, Alessandro Serretti, Concetta Crisafulli   +8 more
wiley   +1 more source

The Impact of Failing to Identify Suspect Effort in Patients Undergoing Adult Attention-Deficit/Hyperactivity Disorder (ADHD) Assessment [PDF]

, 2016
This retrospective study examines how many adult patients would plausibly receive a diagnosis of attention-deficit/hyperactivity disorder (ADHD) if performance and symptom validity measures were not administered during neuropsychological evaluations ...
Heyerdahl, Danielle, Hoelzle, James B, Marshall, Paul S., Nelson, Matthew W.   +3 more
core   +2 more sources

Non‐Invasive Prenatal Testing by Cell‐Free DNA (cfNIPT) for Detecting Turner Syndrome With Mosaicism and Structural Variants—Prenatal Findings and Postnatal Outcomes

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Turner Syndrome (TS) is a sex chromosomal disorder associated with karyotype heterogeneity. Although TS can be associated with severe prenatal findings, most often linked to the 45, X karyotype, the majority of TS fetuses have no overt phenotype, resulting in delayed diagnosis and management.
Ivonne Bedei, Johanna Bruder, Ida C. B. Lund, Simon H. Thomsen, Ida Vogel, Andrea T. Maciel‐Guerra, Francisco Alvarez‐Nava, Melissa L. Crenshaw, Roland Axt‐Fliedner, Claus H. Gravholt, Anne Skakkebæk   +10 more
wiley   +1 more source

Visualizing Turner Syndrome

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Turner syndrome (TS) continues to present a diagnostic challenge to healthcare professionals. The diagnostic challenges associated with TS result in delayed treatment and clinical care. Here we provide an update of the physical appearance of girls and women with TS by presenting clinical photographs and detailed clinical descriptions of 25 ...
Kirstine Stochholm, Astrid Bruun Rasmussen, Anne Skakkebæk   +2 more
wiley   +1 more source

The Technology Crisis in Neuropsychology.

Archives of Clinical Neuropsychology, 2017
Neuropsychology has fallen reliant on outdated and labor intensive methods of data collection that are slow, highly inefficient, and expensive, and provide relatively data-poor estimates of human behavior despite rapid technological advance in most other
Justin B. Miller, W. Barr
semanticscholar   +1 more source