Torthaí cuardaigh - Michael, Mini

Molecular defects in the mannose binding lectin pathway in dermatological disease: Case report and literature review de réir 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 de réir 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... de réir 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... de réir 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 de réir 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 de réir 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 de réir 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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