Zobrazeno 1 - 10
of 68 400
pro vyhledávání: '"HUTTON"'
Publikováno v:
Buildings, Vol 14, Iss 9, p 2729 (2024)
The adoption of digital technologies into construction practices has become a critical area of interest, particularly in addressing challenges related to efficiency, quality, and sustainability. This study focuses on the impacts of digital technologi
Externí odkaz:
https://doaj.org/article/686af38205334f98841c7fddfab4145e
Autor:
Smrithi GM, Ahuja Kriti, Hutton Veena, Padmakumar Megha, Beeravalli Manasa, Goyal Srishti, Sebastian Sheron, Kumar Nithin, Rekha T, Unnikrishnan Bhaskaran, Mithra Prasanna, Holla Ramesh
Publikováno v:
Indian Journal of Community Medicine, Vol 49, Iss 7, Pp 2-3 (2024)
Background: Interrupted classes which gradually shifted to online mode isolating students from their friends during the COVID-19 pandemic has impacted the mental health status of the medical students. Objective: To assess the mental health outcomes a
Externí odkaz:
https://doaj.org/article/4bfeb08c8e36448488b7f6b6345f0e6a
Autor:
Hutton Mann Shaw
Publikováno v:
The Young Researcher, Vol 7, Iss 1, Pp 126-139 (2023)
The link between chess and executive functioning [EF] skills has been hypothesized since the 1990s and studied extensively in children and adults. This relationship is yet to be examined in adolescents. This study–through correlational analysis of
Externí odkaz:
https://doaj.org/article/bcd91331a8184cceb59a8001981516c5
Autor:
Timothy Tidwell, Anthony Gregg, Wayne Grody, Michael Guo, Hutton Kearney, Kristin Monaghan, Jennifer Taylor, Cinthya Zepeda Mendoza, Catherine Ziats, Joshua Deignan, Karen Raraigh
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101576- (2024)
Externí odkaz:
https://doaj.org/article/2bc1c6aac3e3417c8ddb5e2f21d07dc0
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101611- (2024)
Externí odkaz:
https://doaj.org/article/f250eb6f021543cfa90ef1ae0fd501d5
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101723- (2024)
Externí odkaz:
https://doaj.org/article/8a73e14fa34241e4a4c14a2d069a65b8
Autor:
Balcas Justas, Newman Harvey, Bhat Preeti P., Würthwein Frank, Guiang Jonathan, Arora Aashay, Davila Diego, Graham John, Hutton Thomas, Lehman Tom, Yang Xi, Guok Chin, Alexander Mason David, Gutsche Oliver, DeMar Phil, Huang Chih-Hao, Asif Shah Syed, Litvintsev Dmitry, Heath Ryan, Malone Melo Andrew
Publikováno v:
EPJ Web of Conferences, Vol 295, p 01009 (2024)
The Large Hadron Collider (LHC) experiments distribute data by leveraging a diverse array of National Research and Education Networks (NRENs), where experiment data management systems treat networks as a “blackbox” resource. After the High Lumino
Externí odkaz:
https://doaj.org/article/4cfa57710d9e4731ae0fafd6d3a9ddd2
Publikováno v:
Journal of Asthma and Allergy, Vol Volume 15, Pp 1021-1033 (2022)
Bernadette MM Goddard,1,2 Alison Hutton,1 Michelle Guilhermino,1 Vanessa M McDonald1,3,4 1School of Nursing and Midwifery, College of Health, Medicine and Wellbeing, University of Newcastle, Callaghan, NSW, Australia; 2Paediatric Respiratory Departme
Externí odkaz:
https://doaj.org/article/e8aaa61632a849718010a588697d38a0
Autor:
Madeline Q.R. Lopour, Lisa A. Schimmenti, Nicole J. Boczek, Hutton M. Kearney, Arlene V. Drack, Michael C. Brodsky
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 29, Iss , Pp 101745- (2023)
Purpose: To describe a case of Alström syndrome arising from maternal uniparental disomy. Observations: A 13-month-old boy with poor vision and nystagmus was diagnosed with Alström syndrome based on genetic testing that identified a homozygous path
Externí odkaz:
https://doaj.org/article/b128732b228c4ff098da2573bce87b65
Autor:
Christina A. Austin-Tse, Vaidehi Jobanputra, Denise L. Perry, David Bick, Ryan J. Taft, Eric Venner, Richard A. Gibbs, Ted Young, Sarah Barnett, John W. Belmont, Nicole Boczek, Shimul Chowdhury, Katarzyna A. Ellsworth, Saurav Guha, Shashikant Kulkarni, Cherisse Marcou, Linyan Meng, David R. Murdock, Atteeq U. Rehman, Elizabeth Spiteri, Amanda Thomas-Wilson, Hutton M. Kearney, Heidi L. Rehm, Medical Genome Initiative
Publikováno v:
npj Genomic Medicine, Vol 7, Iss 1, Pp 1-13 (2022)
Abstract Whole genome sequencing (WGS) shows promise as a first-tier diagnostic test for patients with rare genetic disorders. However, standards addressing the definition and deployment practice of a best-in-class test are lacking. To address these
Externí odkaz:
https://doaj.org/article/6905d648dde247ee8ce993083466d75f