Kết quả tìm kiếm - Michael, Mini

Molecular defects in the mannose binding lectin pathway in dermatological disease: Case report and literature review Bằng Miller, Christopher, Wilgenbusch, Sara, Michael, Mini, Chi, David S, Youngberg, George, Krishnaswamy, Guha

lấy văn bản lấy văn bản lấy văn bản

Interventions for haemolytic uraemic syndrome and thrombotic thrombocytopenic purpura Bằng Michael, Mini, Elliott, Elizabeth J, Ridley, Greta F, Hodson, Elisabeth M, Craig, Jonathan C

lấy văn bản lấy văn bản lấy văn bản

Deficiency of complement factor H-related proteins and autoantibody-positive hemolytic uremic syndrome in an infant with combined partial deficiencies and autoantibodies to complem... Bằng Michael, Mini, Turner, Nancy, Elenberg, Ewa, Shaffer, Linda G, Teruya, Jun, Arar, Mazen, Hui, Shiu-Ki, Smith, Richard J, Moake, Joel

lấy văn bản lấy văn bản lấy văn bản

Deficiency of complement factor H-related proteins and autoantibody-positive hemolytic uremic syndrome in an infant with combined partial deficiencies and autoantibodies to complem... Bằng Michael, Mini, Turner, Nancy, Elenberg, Ewa, Shaffer, Linda G, Teruya, Jun, Arar, Mazen, Hui, Shiu-Ki, Smith, Richard J, Moake, Joel

lấy văn bản lấy văn bản lấy văn bản

Are conventional stone analysis techniques reliable for the identification of 2,8-dihydroxyadenine kidney stones? A case series Bằng Runolfsdottir, Hrafnhildur L., Lin, Tzu-Ling, Goldfarb, David S., Sayer, John A., Michael, Mini, Ketteridge, David, Rich, Peter R., Edvardsson, Vidar O., Palsson, Runolfur

lấy văn bản lấy văn bản lấy văn bản

Renal Survival in Children with Glomerulonephritis with Crescents: A Pediatric Nephrology Research Consortium Cohort Study Bằng Maliakkal, Joseph G., Hicks, M. John, Michael, Mini, Selewski, David T., Twombley, Katherine, Rheault, Michelle N., Seamon, Meredith, Misurac, Jason M., Tran, Cheryl L., Reyes, Loretta, Flynn, Joseph T., Onder, Ali M., Constantinescu, Alexandru R., Singh, Vaishali, Pan, Cynthia, Omoloja, Abiodun, Wu, Qiang, Smoyer, William E., Hidalgo, Guillermo, Wenderfer, Scott E.

lấy văn bản lấy văn bản lấy văn bản

Whole-Exome Sequencing in the molecular diagnosis of individuals with congenital anomalies of kidney and urinary tract and identification of a new causative gene Bằng Bekheirnia, Mir Reza, Bekheirnia, Nasim, Bainbridge, Matthew N., Gu, Shen, Akdemir, Zeynep Hande Coban, Gambin, Tomek, Janzen, Nicolette K., Jhangiani, Shalini N., Muzny, Donna M., Michael, Mini, Brewer, Eileen D., Elenberg, Ewa, Kale, Arundhati S., Riley, Alyssa A., Swartz, Sarah J., Scott, Daryl A., Yang, Yaping, Srivaths, Poyyapakkam R., Wenderfer, Scott E., Bodurtha, Joann, Applegate, Carolyn D., Velinov, Milen, Myers, Angela, Borovik, Lior, Craigen, William J., Hanchard, Neil A., Rosenfeld, Jill A., Lewis, Richard Alan, Gonzales, Edmond T., Gibbs, Richard A., Belmont, John W., Roth, David R., Eng, Christine, Braun, Michael C., Lupski, James R., Lamb, Dolores J.

lấy văn bản lấy văn bản lấy văn bản