Search Results - Michael, Mini

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  1. 1
    Molecular defects in the mannose binding lectin pathway in dermatological disease: Case report and literature review

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

    Published 2010
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  2. 2
    Interventions for haemolytic uraemic syndrome and thrombotic thrombocytopenic purpura

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

    Published 2009
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  3. 3
    Deficiency of complement factor H-related proteins and autoantibody-positive hemolytic uremic syndrome in an infant with combined partial deficiencies and autoantibodies to complement factor H and ADAMTS13

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

    Published 2018
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  4. 4
    Deficiency of complement factor H-related proteins and autoantibody-positive hemolytic uremic syndrome in an infant with combined partial deficiencies and autoantibodies to complement factor H and ADAMTS13

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

    Published 2018
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  5. 5
    Are conventional stone analysis techniques reliable for the identification of 2,8-dihydroxyadenine kidney stones? A case series

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

    Published 2020
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  6. 6
    Renal Survival in Children with Glomerulonephritis with Crescents: A Pediatric Nephrology Research Consortium Cohort Study

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

    Published 2020
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  7. 7
    Whole-Exome Sequencing in the molecular diagnosis of individuals with congenital anomalies of kidney and urinary tract and identification of a new causative gene

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

    Published 2016
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