Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Andrew Sloas"'
Autor:
Mohsen Saijinejad, Joseph L. Arms, Andrew Sloas, Muhammad Waseem, Brian R. Moore, Nadia M. Pearson, Joseph L. Wright, Hasmig Jinivizian, David P. Mooney, Paula J. Whiteman, Brett Rosen, Paul J. Eakin, Paul Ishimine, Thomas H. Chun, Susan M. Fuchs, Kiyetta Alade, Ariel Cohen, Arthur Cooper, William S. Russell, Denis R. Pauze, Eileen Bulgar, Orel Swenson, Michael Gerardi, Marc H. Gorelick, Jeffrey Hom, Marianne Gausche-Hill, Alice D. Ackerman, David E. Wesson, Ann M. Dietrich, Gerald R. Schwartz, Tres Scherer, Mary E. Fallat, Nanette C. Dudley, Natalie E. Lane, Lee S. Benjamin, Aderonke Ojo, Ritu Sahni, Jeffrey Salomone, Richard M. Cantor, P. David Adelson, Jahn T. Avarello, Isabel A. Barata, Joan E. Shook, Audrey Z. Paul, Madeline Matar Joseph, Dale P. Woolridge, Jonathan H. Valente, Gregory P. Conners, Steven Baldwin, Sanjay Mehta, Kathleen M. Brown, Charles J. Graham, Douglas K. Holtzman
Publikováno v:
Pediatrics. 133:e1104-e1116
This multiorganizational literature review was undertaken to provide an evidence base for determining whether recommendations for out-of-hospital termination of resuscitation could be made for children who are victims of traumatic cardiopulmonary arr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1b09169c8c3e76028383cd520f0afa2
https://doi.org/10.1542/peds.2014-0176
https://doi.org/10.1542/peds.2014-0176
Publikováno v:
Open Journal of Emergency Medicine. :19-27
Spontaneous intracerebral hemorrhage (ICH) accounts for one fifth of all strokes and is associated with an extremely high rate of morbidity and mortality. Affecting greater than 1 million people a year, ICH will leave the majority of its’ patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7492bf1b560dd3b64ea2684db38d924d
https://doi.org/10.4236/ojem.2014.21004
https://doi.org/10.4236/ojem.2014.21004
Publikováno v:
The American journal of emergency medicine. 31(9)
Ornithine transcarbamylase (OTC) deficiency is a genetic disorder involving a mutation of the ornithine transcarbamylase gene, located on the short arm of the X chromosome (Xp21.1). This makes the expression of the gene most common in homozygous male
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52b31506666e0b6e24af833bb9d3bebd
https://pubmed.ncbi.nlm.nih.gov/23790482
https://pubmed.ncbi.nlm.nih.gov/23790482
Autor:
David Delemos, Bindi Naik-Mathuria, Donna Mendez, Linzhi Xu, Harold Andrew Sloas, Daniel M. Rubalcava, Rohit P. Shenoi
Publikováno v:
SAGE Open, Vol 6 (2016)
1. Rohit Shenoi[1][1][⇑][2] 2. Daniel Rubalcava[1][1] 3. Bindi Naik-Mathuria[1][1] 4. Harold A. Sloas[2][3] 5. David Delemos[1][1] 6. Linzhi Xu[1][1] 7. Donna Mendez[3][4] 1. 1Baylor College of Medicine, Houston, TX, USA 2. 2University of Kentucky,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d23eddbcdbec39f6051bd78e642fef60
https://doi.org/10.1177/2158244016653167
https://doi.org/10.1177/2158244016653167