Результати пошуку - Michael, Mini

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

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

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

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

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

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Renal Survival in Children with Glomerulonephritis with Crescents: A Pediatric Nephrology Research Consortium Cohort Study за авторством 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.

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Whole-Exome Sequencing in the molecular diagnosis of individuals with congenital anomalies of kidney and urinary tract and identification of a new causative gene за авторством 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.

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