Zobrazeno 1 - 10
of 164
pro vyhledávání: '"W Craig Hooper"'
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e70061 (2013)
BACKGROUND: Venous thromboembolism (VTE), comprising deep vein thrombosis (DVT) and pulmonary embolism (PE), is a significant source of mortality and morbidity worldwide. By analyzing data of the 2010 Nationwide Inpatient Sample from the Agency for H
Externí odkaz:
https://doaj.org/article/7346bfde21b848bda0c377e6658f270c
Autor:
Jacqueline N Milton, Paola Sebastiani, Nadia Solovieff, Stephen W Hartley, Pallav Bhatnagar, Dan E Arking, Daniel A Dworkis, James F Casella, Emily Barron-Casella, Christopher J Bean, W Craig Hooper, Michael R DeBaun, Melanie E Garrett, Karen Soldano, Marilyn J Telen, Allison Ashley-Koch, Mark T Gladwin, Clinton T Baldwin, Martin H Steinberg, Elizabeth S Klings
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e34741 (2012)
Serum bilirubin levels have been associated with polymorphisms in the UGT1A1 promoter in normal populations and in patients with hemolytic anemias, including sickle cell anemia. When hemolysis occurs circulating heme increases, leading to elevated bi
Externí odkaz:
https://doaj.org/article/e53a001de2c94b03abd90caee3295980
Publikováno v:
PLoS ONE, Vol 7, Iss 7, p e34048 (2012)
BACKGROUND: Deep vein thrombosis and pulmonary embolism (PE) are responsible for substantial mortality, morbidity, and impaired health-related quality of life. The aim of this study was to evaluate the correlates of in-hospital deaths among hospitali
Externí odkaz:
https://doaj.org/article/fb4601eedc894021a0dbbe15fcec7eb5
Autor:
Ya-Lin A. Huang, Hussain Yusuf, Alys Adamski, Joy Hsu, James Baggs, Rehab Auf, Stacey Adjei, Rhett Stoney, W. Craig Hooper, Eloisa Llata, Emilia H. Koumans, Jean Y. Ko, Sebastian Romano, Tegan K. Boehmer, Aaron M. Harris
Publikováno v:
Journal of Thrombosis and Thrombolysis. 55:189-194
The association between thromboembolic events (TE) and COVID-19 infection is not completely understood at the population level in the United States. We examined their association using a large US healthcare database. We analyzed data from the Premier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::811796ed632f93f3bda53f65dcf916bf
https://doi.org/10.1007/s11239-022-02735-0
https://doi.org/10.1007/s11239-022-02735-0
Publikováno v:
Public Health Reports. 137:234-238
Sickle cell disease (SCD) is associated with increased risk of poor health outcomes from respiratory infections, including COVID-19 illness. We used US death data to investigate changes in SCD-related mortality before and during the COVID-19 pandemic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdaf6cd162e69b1f1719e4d3d1900c82
https://doi.org/10.1177/00333549211063518
https://doi.org/10.1177/00333549211063518
Autor:
Laura A. Schieve, Gretchen M. Simmons, Amanda B. Payne, Karon Abe, Lewis L. Hsu, Mary Hulihan, Shammara Pope, Sarah Rhie, Brandi Dupervil, W. Craig Hooper
Publikováno v:
MMWR. Morbidity and mortality weekly report. 71(39)
Sickle cell disease (SCD), a group of inherited blood cell disorders that primarily affects Black or African American persons, is associated with severe complications and a20-year reduction in life expectancy. In 2014, an expert panel convened by the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bf0bf6273fc8868023f020dac7754c3
https://pubmed.ncbi.nlm.nih.gov/36173745
https://pubmed.ncbi.nlm.nih.gov/36173745
Publikováno v:
Pediatrics. 150(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::783bb443c62da9f2c294b1329e37b29d
https://pubmed.ncbi.nlm.nih.gov/36126160
https://pubmed.ncbi.nlm.nih.gov/36126160
Autor:
Lisa C. Richardson, Amanda B. Payne, Dana L. Haberling, Christina Chapman, W. Craig Hooper, Christopher J. Bean, Jason M. Mehal
Publikováno v:
Annals of Emergency Medicine. 76:S28-S36
Study objective We provide an updated assessment of trends in sickle cell disease (SCD)–related mortality, a significant source of mortality in the United States among black persons, using 1979 to 2017 US mortality data. Methods SCD-related deaths
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d08a71bac7768ef563a08673a58f1319
https://doi.org/10.1016/j.annemergmed.2020.08.009
https://doi.org/10.1016/j.annemergmed.2020.08.009
Autor:
Donna DiMichele, Denise E. Sabatino, Diane J. Nugent, W. Keith Hoots, W. Craig Hooper, J. Michael Soucie, Steven W. Pipe
Publikováno v:
Haemophilia
INTRODUCTION: The major complication of protein replacement therapy for haemophilia A is the development of anti-FVIII antibodies or inhibitors that occur in 25%−30% of persons with severe haemophilia A. Alternative therapeutics such as bypassing a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e9bfb98d117c00946119d437e688a27
https://doi.org/10.1111/hae.13737
https://doi.org/10.1111/hae.13737
Autor:
Vanessa R. Byams, Meredith Oakley, Karon Abe, Laura A. Schieve, Connie H. Miller, Brandi Dupervil, Christopher J. Bean, J. Michael Soucie, W. Craig Hooper
Publikováno v:
MMWR Surveillance Summaries
Problem/Condition Hemophilia is an X-linked genetic disorder that primarily affects males and results in deficiencies in blood-clotting proteins. Hemophilia A is a deficiency in factor VIII, and hemophilia B is a deficiency in factor IX. Approximatel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d5437e973d367e7d79d4e433ed27396
https://pubmed.ncbi.nlm.nih.gov/32881847
https://pubmed.ncbi.nlm.nih.gov/32881847