Antithrombin Therapy: Current State and Future Outlook

por Rodgers, George M., Mahajerin, Arash
Publicado 2023

Testing for hereditary thrombophilia: a retrospective analysis of testing referred to a national laboratory

por Jackson, Brian R, Holmes, Kyland, Phansalkar, Amit, Rodgers, George M
Publicado 2008

Prolonged Exposure to Caplacizumab as Rescue Therapy in Refractory Immune Thrombotic Thrombocytopenic Purpura

por Rodgers, George M, Berndt, Misa, Fonteno, Megan, Gilreath, Jeffrey A
Publicado 2023

Acquired von Willebrand syndrome in monoclonal gammopathy – A scoping review on hemostatic management

por Abou‐Ismail, Mouhamed Yazan, Rodgers, George M., Bray, Paul F., Lim, Ming Y.
Publicado 2021

Erythropoiesis-Stimulating Agents in the Management of Anemia in Chronic Kidney Disease or Cancer: A Historical Perspective

por Aapro, Matti, Gascón, Pere, Patel, Kashyap, Rodgers, George M., Fung, Selwyn, Arantes, Luiz H., Wish, Jay
Publicado 2019

Five Challenging Cases of Hereditary Antithrombin Deficiency Characterized by Thrombosis or Complicated Pregnancy

por Roberts, Jonathan C, von Drygalski, Annette, Zhou, Jenny Y, Rodgers, George M, Ansteatt, Kristin, Tarantino, Michael D
Publicado 2022

Building an immune-mediated coagulopathy consensus: early recognition and evaluation to enhance post-surgical patient safety

por Ness, Paul, Creer, Michael, Rodgers, George M, Naoum, Joseph J, Renkens, Kenneth, Voils, Stacy A, Alexander, W Allan
Publicado 2009

SCF-KIT signaling induces endothelin-3 synthesis and secretion: Thereby activates and regulates endothelin-B-receptor for generating temporally- and spatially-precise nitric oxide...

por Chen, Lei L., Zhu, Jing, Schumacher, Jonathan, Wei, Chongjuan, Ramdas, Latha, Prieto, Victor G., Jimenez, Arnie, Velasco, Marco A., Tripp, Sheryl R., Andtbacka, Robert H. I., Gouw, Launce, Rodgers, George M., Zhang, Liansheng, Chan, Benjamin K., Cassidy, Pamela B., Benjamin, Robert S., Leachman, Sancy A., Frazier, Marsha L.
Publicado 2017

ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder

por Williams, Lloyd B., Javed, Asif, Sabri, Amin, Morgan, Denise J., Huff, Chad D., Grigg, John R., Heng, Xiu Ting, Khng, Alexis J., Hollink, Iris H. I. M., Morrison, Margaux A., Owen, Leah A., Anderson, Katherine, Kinard, Krista, Greenlees, Rebecca, Novacic, Danica, Nida Sen, H., Zein, Wadih M., Rodgers, George M., Vitale, Albert T., Haider, Neena B., Hillmer, Axel M., Ng, Pauline C., Shankaracharya, Cheng, Anson, Zheng, Linda, Gillies, Mark C., van Slegtenhorst, Marjon, van Hagen, P. Martin, Missotten, Tom O. A. R., Farley, Gary L., Polo, Michael, Malatack, James, Curtin, Julie, Martin, Frank, Arbuckle, Susan, Alexander, Stephen I., Chircop, Megan, Davila, Sonia, Digre, Kathleen B., Jamieson, Robyn V., DeAngelis, Margaret M.
Publicado 2019