Is kidney biopsy necessary in children with idiopathic nephrotic syndrome? von Bekassy, Zivile, Lindström, Martin, Rosenblad, Therese, Aradóttir, Sunna, Sartz, Lisa, Tullus, Kjell

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Corrigendum: Genetic investigation of Nordic patients with complement-mediated kidney diseases von Rydberg, Viktor, Aradottir, Sigridur Sunna, Kristoffersson, Ann-Charlotte, Svitacheva, Naila, Karpman, Diana

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Genetic investigation of Nordic patients with complement-mediated kidney diseases von Rydberg, Viktor, Aradottir, Sigridur Sunna, Kristoffersson, Ann-Charlotte, Svitacheva, Naila, Karpman, Diana

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Factor D Inhibition Blocks Complement Activation Induced by Mutant Factor B Associated With Atypical Hemolytic Uremic Syndrome and Membranoproliferative Glomerulonephritis von Aradottir, Sigridur Sunna, Kristoffersson, Ann-Charlotte, Roumenina, Lubka T., Bjerre, Anna, Kashioulis, Pavlos, Palsson, Runolfur, Karpman, Diana

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Factor B Mutation in Monozygotic Twins Discordant for Atypical Hemolytic Uremic Syndrome von Aradottir, Sigridur Sunna, Kristoffersson, Ann-Charlotte, Jensson, Brynjar O., Sulem, Patrick, Gong, Henning, Palsson, Runolfur, Karpman, Diana

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Complement dysregulation associated with a genetic variant in factor H-related protein 5 in atypical hemolytic uremic syndrome von Aradottir, Sigridur Sunna, Kristoffersson, Ann-Charlotte, Linnér, Erik, Karpman, Diana

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Phenotypic studies of a novel factor B mutation in familial atypical hemolytic uremic syndrome von Aradottir, Sigridur Sunna, Kristofferson, Ann-Charlotte, Gong, Henning, Roumenina, Lubka T., Palsson, Runolfur, Karpman, Diana

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