Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Ronald H. Lands"'
Autor:
Ronald H. Lands, Michael G. Stabin, Dustin Powell, Bryan Whittle, Aaron Endsley, Alan Stuckey, Ryan R. Julian, Tyler R. Lambeth, Emily B. Martin, Stephen J. Kennel, Angela Williams, Jonathan S. Wall, Sarah Hall
Publikováno v:
Molecular Imaging and Biology. 24:479-488
Purpose Accurate diagnosis of amyloidosis remains a significant clinical challenge and unmet need for patients. The amyloid-reactive peptide p5+14 radiolabeled with iodine-124 has been developed for the detection of amyloid by PET/CT imaging. In a fi
Autor:
Emily B Martin, Angela Williams, Craig Wooliver, R Eric Heidel, Sarah Adams, John Dunlap, Marina Ramirez-Alvarado, Luis M Blancas-Mejia, Ronald H Lands, Stephen J Kennel, Jonathan S Wall
Publikováno v:
PLoS ONE, Vol 12, Iss 3, p e0174152 (2017)
BACKGROUND:Monoclonal free light chain (LC) proteins are present in the circulation of patients with immunoproliferative disorders such as light chain (AL) amyloidosis and multiple myeloma (MM). Light chain-associated amyloid is a complex pathology c
Externí odkaz:
https://doaj.org/article/70a1e18a6c244bd991809094f706fbdf
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 27 (2021)
Clinical and Applied Thrombosis/Hemostasis
Clinical and Applied Thrombosis/Hemostasis
High rates of thromboembolic events have been described in intensive care unit (ICU) patients. Data regarding thromboembolic events in all hospitalized patients has been less frequently reported, raising concerns that thromboembolic events in non-ICU
Autor:
Jonathan S, Wall, Emily B, Martin, Aaron, Endsley, Alan C, Stuckey, Angela D, Williams, Dustin, Powell, Bryan, Whittle, Sarah, Hall, Tyler R, Lambeth, Ryan R, Julian, Michael, Stabin, Ronald H, Lands, Stephen J, Kennel
Publikováno v:
Molecular imaging and biology. 24(3)
Accurate diagnosis of amyloidosis remains a significant clinical challenge and unmet need for patients. The amyloid-reactive peptide p5+14 radiolabeled with iodine-124 has been developed for the detection of amyloid by PET/CT imaging. In a first-in-h
Publikováno v:
Case Reports in Hematology, Vol 2020 (2020)
Case Reports in Hematology
Case Reports in Hematology
Hereditary hyperferritinemia and cataracts syndrome (HHCS) without iron overload is a syndrome first identified less than 3 decades ago. While investigators have dissected the gene where several responsible mutations reside, it remains a relatively u
Autor:
Robert E. Heidel, Alan Stuckey, Tina Richey, Angela Williams, Bryan Whittle, Yitong Fu, Emily B. Martin, Jonathan S. Wall, Stephen J. Kennel, S Guthrie, Ronald H. Lands, Dustin Powell, Myrwood C. Besozzi
Publikováno v:
European Heart Journal. 41
Introduction Systemic amyloidosis is characterized by the deposition of protein fibrils in abdominothoracic organs, notably the heart, leading to organ dysfunction and significant morbidity. Patients who present with light chain (AL) amyloid-associat
Autor:
Alan Stuckey, Ronald H. Lands, R. Eric Heidel, Dustin Powell, Emily B. Martin, Spencer D. Guthrie, Jonathan S. Wall, Stephen J. Kennel, Bryan Whittle
Publikováno v:
Blood. 138:2952-2952
Background: Immunoglobulin light chain-associated (AL) amyloidosis is associated with the deposition of fibrils in abdominothoracic organs, notably the heart, liver, spleen and kidneys, resulting in organ dysfunction and significant morbidity. The he
Autor:
Yitong Fu, James S. Foster, Alan Stuckey, Angela Williams, Dustin Powell, Tina Richey, Bryan Whittle, Emily B. Martin, Spencer D. Guthrie, Jonathan S. Wall, Ronald H. Lands, R. Eric Heidel, Stephen J. Kennel
Publikováno v:
Blood. 136:17-18
Background: Systemic immunoglobulin light chain-associated amyloidosis (AL) is a rare disorder associated with the production of monoclonal free light chain proteins. The aggregation of misfolded light chains leads to the extracellular deposition of
Autor:
Alan Stuckey, Bryan Whittle, Ronald H. Lands, Dustin Powell, Robert E. Heidel, Stephen J. Kennel, Emily B. Martin, Jonathan S. Wall
Publikováno v:
Journal of the American College of Cardiology. 77:1287
Autor:
Eric D. Tague, Abigail T. Farmer, Shawn R. Campagna, Emily B. Martin, Craig Wooliver, R. Eric Heidel, James S. Foster, Ronald H. Lands, Jonathan S. Wall, Alan Stuckey, Angela Williams, Stephen J. Kennel, Sallie Macy, Tina Richey
Publikováno v:
Proceedings of the National Academy of Sciences. 115
Amyloidosis is a malignant pathology associated with the formation of proteinaceous amyloid fibrils that deposit in organs and tissues, leading to dysfunction and severe morbidity. More than 25 proteins have been identified as components of amyloid,