Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Margo Renee Rollins"'
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Scientific Reports
Scientific Reports
Smartphone-based telehealth holds the promise of shifting healthcare from the clinic to the home, but the inability for clinicians to conduct remote palpation, or touching, a key component of the physical exam, remains a major limitation. This is exe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea8fd4548361974f3927fb373c0bab03
https://doi.org/10.1038/s41598-017-13076-x
https://doi.org/10.1038/s41598-017-13076-x
Autor:
Margo Renee Rollins, Jonathan Bae, Radhika Shah, Laura M. De Castro, Daniel Landi, Nirmish Shah
Publikováno v:
The Clinical Journal of Pain. 30:266-268
Sickle cell disease (SCD) is a chronic disease characterized by multiple vaso-occlusive complications and is increasingly cared for by hospitalists. The purpose of this study is to examine differences in pain management between hematologists and hosp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3be83c53aebfa18c4c63cc37bfefc08
https://doi.org/10.1097/ajp.0b013e318295ec04
https://doi.org/10.1097/ajp.0b013e318295ec04
Autor:
Lucas H. Timmins, Robert G. Mannino, Wilbur A. Lam, Robert E. Guldberg, Yichen Wang, Don P. Giddens, Angela S.P. Lin, Byungwook Ahn, David R. Myers, Hope K.A. Gole, Margo Renee Rollins
Publikováno v:
Scientific Reports
Investigating biophysical cellular interactions in the circulation currently requires choosing between in vivo models, which are difficult to interpret due in part to the hemodynamic and geometric complexities of the vasculature; or in vitro systems,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ff8151e95b4e18195a58bf4b7d97d34
http://europepmc.org/articles/PMC4894411
http://europepmc.org/articles/PMC4894411
Publikováno v:
Blood. 126:215-215
Background: The genetic mutation of sickle cell disease (SCD) leads to polymerized hemoglobin, causing altered erythrocyte shape, increased stiffness, and dehydration, all of which are associated with vascular occlusion and negative clinical outcomes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::570a2c27a7928440205e38a2b413f748
https://doi.org/10.1182/blood.v126.23.215.215
https://doi.org/10.1182/blood.v126.23.215.215
Publikováno v:
Blood. 126:3381-3381
Introduction: Sickle Cell Disease (SCD) is an inherited monogenic hemoglobin disorder characterized by decreased red blood cells (RBCs) deformability. While RBCs are directly affected by this mutation, the interaction of these cells in the milieu of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d98fd7dd358b6342f1bc37bac751caf0
https://doi.org/10.1182/blood.v126.23.3381.3381
https://doi.org/10.1182/blood.v126.23.3381.3381
Publikováno v:
Blood. 124:4155-4155
Sickle Cell Disease (SCD) is an inherited disorder of the β-globin chain of hemoglobin, in which a single point mutation leads to decreased deformability of red blood cells (RBCs) and increased cellular adhesion to endothelium. The effect of this mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75db2151514bb95af8d3ec707fe0b189
https://doi.org/10.1182/blood.v124.21.4155.4155
https://doi.org/10.1182/blood.v124.21.4155.4155
Publikováno v:
Blood. 118:4185-4185
Abstract 4185 INTRODUCTION: Sickle cell disease (SCD) is a chronic disease characterized by multiple vaso-occlusive complications. Often patients present with episodic pain which can be severe, disabling, and often require opioid treatment. Furthermo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d99c6c1ddf86dfb033f1af06a2f460f8
https://doi.org/10.1182/blood.v118.21.4185.4185
https://doi.org/10.1182/blood.v118.21.4185.4185