Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Lauren Haus"'
Publikováno v:
Health Behavior Research, Vol 6, Iss 4 (2023)
College students who experience stigma report problematic alcohol use. However, the stigma- health link focuses on one form of stigma, thereby excluding the intersectional oppression of experiencing multiple forms of stigma. The present work has two
Externí odkaz:
https://doaj.org/article/9907eb9dca2a438a8bdccd561092a51e
Autor:
Shannon Speed, Rose Marie Ward, Lauren Haus, Paul Branscum, Veronica Barrios, Kristen M. Budd, Kayla Lemons, Emma Humenay
Publikováno v:
American Journal of Health Education. 53:342-359
Autor:
Valeria Guglielmi, Luca Colangeli, Valeria Scipione, Simona Ballacci, Martina Di Stefano, Lauren Hauser, Michela Colella Bisogno, Monica D'Adamo, Emanuela Medda, Paolo Sbraccia
Publikováno v:
PLoS ONE, Vol 17, Iss 5, p e0268432 (2022)
IntroductionDuring COVID-19 pandemic, Internal Medicine Units (IMUs) accounted for about 70% of patients hospitalized. Although a large body of data has been published regarding the so-called first wave of the pandemic, little is known about the char
Externí odkaz:
https://doaj.org/article/ff33b97eca9c48f08f0fa1bbbbba7288
Autor:
Mallika L Mendu, Emily Fay, Constantinos I Michaelidis, Michele C Chu, Jasdeep Sahota, Lauren Hauser, Aimee Smith, Mary Ann Huether, John Dobija, Mark Yurkofsky, Charles T Pu, Kathryn Britton
Publikováno v:
BMJ Open Quality, Vol 7, Iss 3 (2018)
30-day readmissions for patients at skilled nursing facilities (SNF) are common and preventable. We implemented a readmission review process for patients readmitted from two SNFs, involving an electronic review tool and monthly conferences. The elect
Externí odkaz:
https://doaj.org/article/8c87162e18734bc6847aae100d43df34
Autor:
Ashlee Long, Jill S Napierala, Urszula Polak, Lauren Hauser, Arnulf H Koeppen, David R Lynch, Marek Napierala
Publikováno v:
PLoS ONE, Vol 12, Iss 12, p e0189990 (2017)
Friedreich's ataxia (FRDA) is a genetic neurodegenerative disorder caused by transcriptional silencing of the frataxin gene (FXN) due to expansions of GAA repeats in intron 1. FRDA manifests with multiple symptoms, which may include ataxia, cardiomyo
Externí odkaz:
https://doaj.org/article/df6afd54e6fb4223aed6fa368d898031