COVID-19 mRNA vaccination responses in individuals with sickle cell disease: an ASH RC Sickle Cell Research Network Study

Autor: Anderson, Alan R., Andemariam, Biree, Brandow, Amanda, Campbell, Andrew, Cohen, Alice, Darbari, Deepika, El Rassi, Fuad, ield, Joshua, Fung, Ellen, Gee, Beatrice, Ibrahim, Ibrahim, Idowu, Modupe, Kanter, Julie, Klings, Elizabeth S., King, Allison, Kutlar, Abdullah, Lebensburger, Jeffrey D., Leavey, Patrick, Liem, Robert I., Manwani, Deepa, Narang, Shalu, Pace, Betty, Quinn, Charles T., Rivlin, Kenneth, Strouse, John J., Thompson, Alexis A., Tubman, Venée N., Vichinsky, Elliot, Walters, Mark, Brandow, Amanda M., Vichinsky, Elliott, Leavey, Patrick J., Nero, Alecia, Ibrahim, Ibrahim F., Field, Joshua J., Baer, Amanda, Soto-Calderon, Haideliza, Vincent, Lauren, Zhao, Yan, Santos, Jefferson J. S., Hensley, Scott E., Mortier, Nicole, Lanzkron, Sophie, Neuberg, Donna, Abrams, Charles S.

Publikováno v: In Blood Advances 10 September 2024 8(17):4549-4553

A multilevel mHealth intervention boosts adherence to hydroxyurea in individuals with sickle cell disease

Autor: Hankins, Jane S., Hodges, Jason, Carroll, Yvonne, Klesges, Lisa, Khan, Hamda, Smeltzer, Matthew, Nwosu, Chinonyelum, Gurney, James, Porter, Jerlym, Alberts, Nicole, French, Reginald, Badawy, Sherif, DeBaun, Michael, Kang, Guolian, Estepp, Jeremie, Wang, Winfred, Owens, Curtis, Debon, Margaret, Osarogiagbon, Ray, Nelson, Marquita, Treadwell, Marsha, Vichinsky, Elliott, Wun, Ted, Potter, Michael, Hessler, Danielle, Hagar, Ward, Marsh, Anne, Neumayr, Lynne, Melvin, Cathy, Kanter, Julie, Phillips, Shannon, Adams, Robert, Mueller, Martina, Abrams, Tina, Davia, Nathalia, Shah, Nirmish, Tanabe, Paula, Bosworth, Hayden, Jackson, George, Johnson, Fred, Richesson, Rachel, Prvu-Bettger, Janet, King, Allison, Baumann, Ana, Calhoun, Cecilia, Kutlar, Abdullah, Gibson, Robert, Snyder, Angie, Fernandez, Maria, Lottenberg, Richard, Richardson, Lynne D., Glassberg, Jeffrey, Simon, Jena, Genes, Nicholas G., Loo, George T., Shapiro, Jason S., Souffront, Kimberly, Clesca, Cindy, Linton, Elizabeth, Ryan, Gery, Kroner, Barbara L, Hendershot, Tabitha, DiMartino, Lisa, Jacobs, Sara, Battestilli, Whitney, Brambilla, Donald, Cox, Lisa, Preiss, Liliana, Pugh, Norma, Li, Sophie, VonLehmden, Annie, Smith, Sharon M, Tonkins, William P., Peters-Lawrence, Marlene, Boyce, Cheryl, Barfield, Whitney, Thompson, Alexis, Gordeuk, Victor, Gutierrez, Melissa, Hirschtick, Jana, Hsu, Lewis, Krishnan, Jerry, Sebro, Nadew, Verda, Larissa, Wandersman, Abe, Berbaum, Michael, Bobba, Kishore, Colla, Joe, Erwin, Kim, Lamont, Andrea, Martin, Molly, Norell, Sarah, Pandit, Ananta, Saving, Kay, Shannon, Robin, Winn, Robert, Zun, Leslie, Hassan, Taif, Lasley, Patricia, Monnard, Kristin, Nocek, Judith, Roesch, Pamela, Potter, Michael B., King, Allison A., Baumann, Ana A., Gordeuk, Victor R., Hsu, Lewis L., Porter, Jerlym S., Alberts, Nicole M., Badawy, Sherif M., Glassberg, Jeffrey A., Fernandez, Maria E., Bosworth, Hayden B., Klesges, Lisa M.

Publikováno v: In Blood Advances 12 December 2023 7(23):7190-7201

Genetic risk factors for cerebrovascular disease in children with sickle cell disease: design of a case-control association study and genomewide screen

Autor: Brambilla Donald, Clair Betsy, McKie Virgil C, Snieder Harold, Adams Gaye T, Adams Robert J, Kutlar Ferdane, Kutlar Abdullah

Publikováno v: BMC Medical Genetics, Vol 4, Iss 1, p 6 (2003)

Abstract Background The phenotypic heterogeneity of sickle cell disease is likely the result of multiple genetic factors and their interaction with the sickle mutation. High transcranial doppler (TCD) velocities define a subgroup of children with sic

Externí odkaz: https://doaj.org/article/58231dbef0fb48d9a98b944cf3057b48

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.