Torthaí cuardaigh - Rodgers, George M.

Testing for hereditary thrombophilia: a retrospective analysis of testing referred to a national laboratory de réir Jackson, Brian R, Holmes, Kyland, Phansalkar, Amit, Rodgers, George M

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Weight-based dosing of enoxaparin for VTE prophylaxis in morbidly obese, medically-Ill patients de réir Rondina, Matthew T., Wheeler, Michelle, Rodgers, George M., Draper, Leslie, Pendleton, Robert C.

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Acquired von Willebrand syndrome in monoclonal gammopathy – A scoping review on hemostatic management de réir Abou‐Ismail, Mouhamed Yazan, Rodgers, George M., Bray, Paul F., Lim, Ming Y.

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High prevalence of overweight/obesity in adult persons with hemophilia in Utah and a review of the literature de réir Lim, Ming Y., Wei, Guo, Presson, Angela P., Bray, Paul, Rodgers, George M.

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Erythropoiesis-Stimulating Agents in the Management of Anemia in Chronic Kidney Disease or Cancer: A Historical Perspective de réir Aapro, Matti, Gascón, Pere, Patel, Kashyap, Rodgers, George M., Fung, Selwyn, Arantes, Luiz H., Wish, Jay

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Building an immune-mediated coagulopathy consensus: early recognition and evaluation to enhance post-surgical patient safety de réir Ness, Paul, Creer, Michael, Rodgers, George M, Naoum, Joseph J, Renkens, Kenneth, Voils, Stacy A, Alexander, W Allan

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An Inherited Disorder With Splenomegaly, Cytopenias, and Vision Loss de réir Tantravahi, Srinivas K., Williams, Lloyd B., Digre, Kathleen B., Creel, Donnell J., Smock, Kristi J., DeAngelis, Margaret M., Clayton, Frederic C., Vitale, Albert T., Rodgers, George M.

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

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

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