Rezultati - Michael, Mini

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

Polni tekst Polni tekst Polni tekst

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

Polni tekst Polni tekst Polni tekst

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

Polni tekst Polni tekst Polni tekst

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

Polni tekst Polni tekst Polni tekst

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

Polni tekst Polni tekst Polni tekst

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

Polni tekst Polni tekst Polni tekst

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

Polni tekst Polni tekst Polni tekst