Zobrazeno 1 - 10
of 259
pro vyhledávání: '"E. Rappaport"'
Autor:
Christopher Poyorena, Aimee Anderson, Jordan R. Pollock, James L. Homme, Douglas E. Rappaport, John Shufeldt, Rachel A. Lindor
Publikováno v:
Journal of the American College of Emergency Physicians Open, Vol 4, Iss 4, Pp n/a-n/a (2023)
Abstract Background This study characterizes medical malpractice lawsuits involving trainees providing care in the emergency department (ED), affording insight into the types of patients involved, clinical scenarios, and legal outcomes of these cases
Externí odkaz:
https://doaj.org/article/d216281aef984408a5c12670348ceda7
Autor:
Douglas E. Rappaport
Publikováno v:
Journal of Clinical Research and Reports. 12:01-06
Background:Overcrowding in Emergency Departments is associated with poor patient outcomes and low patient satisfaction; overcrowding has been exacerbated by the ongoing Covid-19 pandemic. One intervention used in both the H1N1 pandemic and the curren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::531fe6e65b8b84d7d4b7bb059ed1c863
https://doi.org/10.31579/2690-1919/294
https://doi.org/10.31579/2690-1919/294
Publikováno v:
SIAM Journal on Scientific Computing. 43:B354-B380
Resistive magnetohydrodynamics (MHD) is a continuum base-level model for conducting fluids (e.g., plasmas and liquid metals) subject to external magnetic fields. The efficient and robust solution o...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab705b33999084af1e323556aeb4c55a
https://doi.org/10.1137/20m1342975
https://doi.org/10.1137/20m1342975
Publikováno v:
The Journal of emergency medicine. 57(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c77f6b3d91d0c91f8f92dcec10da5466
https://pubmed.ncbi.nlm.nih.gov/31003814
https://pubmed.ncbi.nlm.nih.gov/31003814
Publikováno v:
The Journal of emergency medicine. 52(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6b298022b26b3f344a5ad49c004c685
https://pubmed.ncbi.nlm.nih.gov/28057370
https://pubmed.ncbi.nlm.nih.gov/28057370
Autor:
Kai Wang, Cecilia Kim, Kristina A. Cole, Jill E. Lynch, Jonathan P. Bradfield, Alexandra I. F. Blakemore, Patrick McGrady, Maura Diamond, Kristopher R. Bosse, Katlyn Pecor, Hakon Hakonarson, Marci Laudenslager, Sharon J. Diskin, Hongzhe Li, Cuiping Hou, Edward F. Attiyeh, John M. Maris, Cynthia Winter, Andrew Wood, Wendy B. London, Marcella Devoto, Yael P. Mosse, Tamim H. Shaikh, Struan F.A. Grant, Elizabeth A. Geiger, E. Rappaport, Joseph T. Glessner
Publikováno v:
Nature. 459:987-991
Copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) are two important potential sources of phenotypic variation in humans. Until now, only SNPs have been associated with cancer, but the increasing recognition that germline DNA do
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a201763cbc7dd0802a8345812a88f8c
https://doi.org/10.1038/nature08035
https://doi.org/10.1038/nature08035
Autor:
David L. Barker, Elaine S. Mansfield, S Enad, Marina Vainer, E. Rappaport, Paolo Fortina, Dennis W. Harris
Publikováno v:
Genome Research. 6:893-903
The Human Genome Initiative has increased significantly the rate at which disease-causing genes are being mapped and sequenced. New cost-effective methods to locate the genes and to characterize disease-causing mutations require robust, reproducible,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::291baeec7260977ed152bb21d0ebb711
https://doi.org/10.1101/gr.6.9.893
https://doi.org/10.1101/gr.6.9.893
Publikováno v:
Psychiatric Rehabilitation Journal. 20:11-18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c86cdf4b435bcb137f14501e974427c8
https://doi.org/10.1037/h0095407
https://doi.org/10.1037/h0095407
Autor:
T Parrella, Elias Schwartz, Saul Surrey, E. Rappaport, Rebecca Conant, Paolo Fortina, G Dotti, G Monokian, Wendy Hitchcock
Publikováno v:
Genome Research. 2:163-166
A rapid, simple, cost-effective, non-radioactive method for detection of the most common mutations causing beta-thalassemia in Mediterranean people has been developed by combining multiplexing with the amplification refractory system. This approach,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c90be0d5fd8673fe01d393d1c8b4ef2
https://doi.org/10.1101/gr.2.2.163
https://doi.org/10.1101/gr.2.2.163
Although autism is a highly heritable neurodevelopmental disorder, attempts to identify specific susceptibility genes have thus far met with limited success. Genome-wide association studies using half a million or more markers, particularly those wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::f4f7dc6aadcbed29bd55d9e47541fb1e
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3057162
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3057162
