Zobrazeno 1 - 10
of 25
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
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
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,
Autor:
Emmanuel Isang, Ronald H. Lands
Publikováno v:
Case Reports in Hematology
Case Reports in Hematology, Vol 2017 (2017)
Case Reports in Hematology, Vol 2017 (2017)
Iron may accumulate in excess due to a mutation in the HFE gene that upregulates absorption or when it is ingested or infused at levels that exceed the body’s ability to clear it. Excess iron deposition in parenchymal tissue causes injury and ultim
Autor:
R. Eric Heidel, Alan Stuckey, Yitong Fu, Radhakrishnan Ramchandren, Tina Richey, Barbara Marine, Mark Powell, James S. Foster, Dustin Osborne, Robin Geldrich, Daniel Craig Wooliver, Dustin Powell, Myrwood C. Besozzi, Emily B. Martin, Stephen J. Kennel, Ronald H. Lands, Angela Williams, Jonathan S. Wall, Sallie Macy, Bryan Whittle
Publikováno v:
Blood. 134:3034-3034
Background: Systemic immunoglobulin light chain-associated amyloidosis (AL) is a rare disorder associated with plasma cell dyscrasias and the production of monoclonal free light chain proteins. Pathology results from the extracellular deposition of p