Increasing prevalence of hypertension during long-term follow-up in children with autosomal dominant polycystic kidney disease von Seeman, Tomáš, Jansky, Petr, Filip, Fencl, Bláhová, Květa, Jaroš, Adam

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Enterohemorrhagic Escherichia coli as causes of hemolytic uremic syndrome in the Czech Republic von Marejková, Monika, Bláhová, Květa, Janda, Jan, Fruth, Angelika, Petráš, Petr

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Mutations in the human laminin β2 (LAMB2) gene and the associated phenotypic spectrum von Matejas, Verena, Hinkes, Bernward, Alkandari, Faisal, Al-Gazali, Lihadh, Annexstad, Ellen, Aytac, Mehmet B., Barrow, Margaret, Bláhová, Květa, Bockenhauer, Detlef, Cheong, Hae Il, Maruniak-Chudek, Iwona, Cochat, Pierre, Dötsch, Jörg, Gajjar, Priya, Hennekam, Raoul C., Janssen, Françoise, Kagan, Mikhail, Kariminejad, Ariana, Kemper, Markus J., Koenig, Jens, Kogan, Jillene, Kroes, Hester Y., Kuwertz-Bröking, Eberhard, Lewanda, Amy F., Medeira, Ana, Muscheites, Jutta, Niaudet, Patrick, Pierson, Michel, Saggar, Anand, Seaver, Laurie, Suri, Mohnish, Tsygin, Alexey, Wühl, Elke, Zurowska, Aleksandra, Uebe, Steffen, Hildebrandt, Friedhelm, Antignac, Corinne, Zenker, Martin

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Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertension von Seeman, Tomáš, Bláhová, Kveta, Fencl, Filip, Klaus, Richard, Lange-Sperandio, Bärbel, Hrčková, Gabriela, Podracká, Ĺudmila

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Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosis von Obeidova, Lena, Seeman, Tomas, Fencl, Filip, Blahova, Kveta, Hojny, Jan, Elisakova, Veronika, Reiterova, Jana, Stekrova, Jitka

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Ophthalmological Aspects of Pierson Syndrome von Bredrup, Cecilie, Matejas, Verena, Barrow, Margaret, Bláhová, Květa, Bockenhauer, Detlef, Fowler, Darren J, Gregson, Richard M, Maruniak-Chudek, Iwona, Medeira, Ana, Mendonça, Erica Laima, Kagan, Mikhail, Koenig, Jens, Krastel, Hermann, Kroes, Hester Y, Saggar, Anand, Sawyer, Taylor, Schittkowski, Michael, Świetliński, Janusz, Thompson, Dorothy, VanDeVoorde, Rene G, Wittebol-Post, Dienke, Woodruff, Geoffrey, Zurowska, Aleksandra, Hennekam, Raoul C, Zenker, Martin, Russell-Eggitt, Isabelle

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Cattle Can Be a Reservoir of Sorbitol-Fermenting Shiga Toxin-Producing Escherichia coli O157:H−Strains and a Source of Human Diseases von BIELASZEWSKA, M, SCHMIDT, H, LIESEGANG, A, PRAGER, R, RABSCH, W, TSCHÄPE, H, CIZEK, A, JANDA, J, BLAHOVA, K, KARCH, H

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Various phenotypes of disease associated with mutated DGKE gene von Bezdíčka, Martin, Pavlíček, Petr, Bláhová, Květa, Háček, Jaromír, Zieg, Jakub

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Severe hypercalcemic crisis in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 gene von Fencl, Filip, Bláhová, Květa, Schlingmann, Karl Peter, Konrad, Martin, Seeman, Tomáš

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Blood pressure in children with renal cysts and diabetes syndrome von Seeman, Tomáš, Weigel, Friederike, Blahova, Kveta, Fencl, Filip, Pruhova, Stepanka, Hermes, Katharina, Klaus, Richard, Lange-Sperandio, Bärbel, Grote, Veit, John-Kroegel, Ulrike

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Attack of the clones: whole genome-based characterization of two closely related enterohemorrhagic Escherichia coli O26 epidemic lineages von Karnisova, Lucia, Marejkova, Monika, Hrbackova, Hana, Mellmann, Alexander, Karch, Helge, Fruth, Angelika, Drevinek, Pavel, Blahova, Kveta, Bielaszewska, Martina, Nunvar, Jaroslav

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Genotype–phenotype correlation in children with autosomal dominant polycystic kidney disease von Fencl, Filip, Janda, Jan, Bláhová, Květa, Hříbal, Zdeněk, Štekrová, Jitka, Puchmajerová, Alena, Seeman, Tomáš

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Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome von Fencl, Filip, Malina, Michal, Stará, Veronika, Zieg, Jakub, Mixová, Dana, Seeman, Tomáš, Bláhová, Květa

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Incidence and severity of pertussis hospitalisations in infants aged less than 1 year in 37 hospitals of six EU/EEA countries, results of PERTINENT sentinel pilot surveillance syst... von Merdrignac, Lore, Aït El Belghiti, Fatima, Pandolfi, Elisabetta, Jané, Mireia, Murphy, Jane, Fabiánová, Kateřina, García Cenoz, Manuel, Flem, Elmira, Guillot, Sophie, Tozzi, Alberto E, Carmona, Gloria, Habington, Adele, Zavadilová, Jana, Navasués, Ana, Bøås, Håkon, Lévy-Brühl, Daniel, Ferretti, Beatrice, Lanaspa, Miguel, O'Sullivan, Niam, Křížová, Pavla, Fernandino, Leticia, Bekkevold, Terese, Hanslik, Thomas, Muñoz-Almagro, Carmen, Bacci, Sabrina, Spiteri, Gianfranco, Valenciano, Marta, Moren, Alain

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Polycystic kidney and hepatic disease with mental retardation and hand anomalies in three siblings von Seeman, Tomáš, Malíková, Marcela, Bláhová, Květa, Seemanová, Eva

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Fatal case of diarrhea-associated hemolytic uremic syndrome with severe neurologic involvement von Zieg, Jakub, Dusek, Jiri, Marejkova, Monika, Limrova, Petra, Blazek, Daniel, Pavlicek, Petr, Grega, Marek, Janda, Jan, Blahova, Kveta

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Ambulatory blood pressure monitoring in children with unilateral multicystic dysplastic kidney von SEEMAN, Tomas, JOHN, Ulrike, BLAHOVA, Kveta, VONDRICHOVA, Hana, JANDA, Jan, MISSELWITZ, Joachim

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Complement activation is associated with more severe course of diarrhea-associated hemolytic uremic syndrome, a preliminary study von Karnisova, Lucia, Hradsky, Ondrej, Blahova, Kveta, Fencl, Filip, Dolezel, Zdenek, Zaoral, Tomas, Zieg, Jakub

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Long-term follow-up of Czech children with D+ hemolytic-uremic syndrome von BLAHOVA, Kveta, JANDA, Jan, KREISINGER, Jiri, MATEJKOVA, Eva, SEDIVA, Anna

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Urinary transforming growth factor-β1 in children with obstructive uropathy von ZIEG, JAKUB, BLAHOVA, KVETA, SEEMAN, TOMAS, BRONSKY, JIRI, DVORAKOVA, HANA, PECHOVA, MARTA, JANDA, JAN, MATOUSOVIC, KAREL

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