Thomas E. Robey
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Thomas E. Robey has a total of 14 co-authors. Here are the top co-authors by number of shared publications:
- Charles E. Murry
University of Washington
3 shared publications Hans Reinecke
Department of Pathology, Center for Cardiovascular Biology and Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA 98109, USA
2 shared publications- Charles E. Murry
Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, USA
1 shared publication Edward R. Melnick
Department of Emergency Medicine, Yale University, 464 Congress Avenue, Steuite 260, New Haven, CT 06519-1315, USA
1 shared publication- Jay M. Brenner
SUNY Upstate Med Univ, Dept Emergency Med, Syracuse, NY USA
1 shared publication Jeff N. Anderl
Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA
1 shared publication
Latest Publications
- 23 September 2023
- Published by Elsevier in Emergency Medicine Clinics of North America
- Vol. 42 (1) , 197-207
Legal and Ethical Considerations in Psychiatric Emergencies
- 23 September 2023
- Published by Elsevier in Emergency Medicine Clinics of North America
- Vol. 42 (1) , 197-207
Legal and Ethical Considerations in Psychiatric Emergencies
- 1 January 2013
- Published by Elsevier in Cardiovascular Pathology
- Vol. 22 (1) , 91-95
Lack of thrombospondin-2 reduces fibrosis and increases vascularity around cardiac cell grafts
- 1 January 2013
- Published by Elsevier in Cardiovascular Pathology
- Vol. 22 (1) , 91-95
Lack of thrombospondin-2 reduces fibrosis and increases vascularity around cardiac cell grafts
- Open Access
- 28 June 2012
- Published by Wiley in Case Reports in Emergency Medicine
- Vol. 2012, 1-3
Undifferentiated Altered Mental Status: A Late Presentation of Toxic Acetaminophen Ingestion
Altered mental status is a common undifferentiated presentation in the emergency department. We describe a case of acetaminophen-induced acute liver failure that was diagnosed and treated prior to obtaining definitive historical or laboratory information about the etiology. The physical exam finding of scleral icterus in this case was a key element to rapid identification and treatment of this life-threatening condition. A discussion of appropriate N-acetylcysteine treatment for acute liver failure and acetaminophen intoxication is included.
- 28 June 2012
- Published by Wiley in Case Reports in Emergency Medicine
- Vol. 2012, 1-3
Open AccessUndifferentiated Altered Mental Status: A Late Presentation of Toxic Acetaminophen Ingestion
Altered mental status is a common undifferentiated presentation in the emergency department. We describe a case of acetaminophen-induced acute liver failure that was diagnosed and treated prior to obtaining definitive historical or laboratory information about the etiology. The physical exam finding of scleral icterus in this case was a key element to rapid identification and treatment of this life-threatening condition. A discussion of appropriate N-acetylcysteine treatment for acute liver failure and acetaminophen intoxication is included.
- 1 October 2008
- Published by Elsevier in Journal of Molecular and Cellular Cardiology
- Vol. 45 (4) , 567-581
Systems approaches to preventing transplanted cell death in cardiac repair
- 1 October 2008
- Published by Elsevier in Journal of Molecular and Cellular Cardiology
- Vol. 45 (4) , 567-581
Systems approaches to preventing transplanted cell death in cardiac repair
- 11 March 2008
- Published by Wiley in Journal of Biomedical Materials Research Part A
- Vol. 88A (3) , 704-710
Retention and biodistribution of microspheres injected into ischemic myocardium
Intramyocardial injection of therapeutic agents may enhance heart repair after infarction. Incomplete retention of intramyocardial injections has been reported, but modes of loss are undefined. We determined the fate of neutron‐activated microspheres injected into acutely ischemic rat myocardium using saline, Pluronic F127, or Matrigel as vehicle. Twenty minutes after injection in saline, 63% ± 12% of 10‐μm microspheres was retained in the heart. Similar retention was observed after 6 days. Injection site leakage accounted for 14% ± 5% of the microspheres, whereas exit via coronary veins resulted in 11.2% ± 9.5% collecting in the lungs. Microspheres distribution to other organs was minimal. Retention of 40‐μm microspheres was similar to that observed with the 10‐μm microspheres. Pluronic F127 and Matrigel reduced immediate leakage to 4% ± 1% and 2% ± 1%, respectively. Surprisingly, microsphere retention in the heart was not improved at 20 min using either gelling vehicle, suggesting that leakage occurs over a prolonged period. Thus, most injected particles are retained in the ischemic rat heart following direct injection, but significant fractions are lost from the injection site and through coronary veins. Gelling agents reduced short‐term leakage, but failed to enhance longer‐term retention. Hydrogels with stiffer mechanical properties might enhance retention and reduce variability. © 2008 Wiley Periodicals, Inc. J Biomed Mater Res, 2009
- 11 March 2008
- Published by Wiley in Journal of Biomedical Materials Research Part A
- Vol. 88A (3) , 704-710
Retention and biodistribution of microspheres injected into ischemic myocardium
Intramyocardial injection of therapeutic agents may enhance heart repair after infarction. Incomplete retention of intramyocardial injections has been reported, but modes of loss are undefined. We determined the fate of neutron‐activated microspheres injected into acutely ischemic rat myocardium using saline, Pluronic F127, or Matrigel as vehicle. Twenty minutes after injection in saline, 63% ± 12% of 10‐μm microspheres was retained in the heart. Similar retention was observed after 6 days. Injection site leakage accounted for 14% ± 5% of the microspheres, whereas exit via coronary veins resulted in 11.2% ± 9.5% collecting in the lungs. Microspheres distribution to other organs was minimal. Retention of 40‐μm microspheres was similar to that observed with the 10‐μm microspheres. Pluronic F127 and Matrigel reduced immediate leakage to 4% ± 1% and 2% ± 1%, respectively. Surprisingly, microsphere retention in the heart was not improved at 20 min using either gelling vehicle, suggesting that leakage occurs over a prolonged period. Thus, most injected particles are retained in the ischemic rat heart following direct injection, but significant fractions are lost from the injection site and through coronary veins. Gelling agents reduced short‐term leakage, but failed to enhance longer‐term retention. Hydrogels with stiffer mechanical properties might enhance retention and reduce variability. © 2008 Wiley Periodicals, Inc. J Biomed Mater Res, 2009
- 1 January 2008
- Published by Elsevier in Cardiovascular Pathology
- Vol. 17 (1) , 6-13
Absence of regeneration in the MRL/MpJ mouse heart following infarction or cryoinjury
- 1 January 2008
- Published by Elsevier in Cardiovascular Pathology
- Vol. 17 (1) , 6-13
Absence of regeneration in the MRL/MpJ mouse heart following infarction or cryoinjury
- 13 September 1996
- Published by Elsevier in Journal of Chromatography A
- Vol. 744 (1-2) , 177-185
Comparative peptide mapping of a hepatitis C viral recombinant protein by capillary electrophoresis and matrix-assisted laser desorption time-of-flight mass spectrometry
- 13 September 1996
- Published by Elsevier in Journal of Chromatography A
- Vol. 744 (1-2) , 177-185
Comparative peptide mapping of a hepatitis C viral recombinant protein by capillary electrophoresis and matrix-assisted laser desorption time-of-flight mass spectrometry