Search Results - "BLAHOVA, Kveta"

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

“…Introduction Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease. Kidney cysts form over the course of the…”
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Ambulatory blood pressure and hypertension control in children with autosomal recessive polycystic kidney disease: clinical experience from two central European tertiary centres by Seeman, Tomáš, Blažík, Radek, Fencl, Fencl, Bláhová, Květa, Obeidová, Lena, Štekrová, Jitka, Weigel, Friederike, John-Kroegel, Ulrike

“…: Arterial hypertension is a common complication in patients with autosomal recessive polycystic kidney disease (ARPKD), occurring in 33-75% of children when…”
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Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosis by Obeidova, Lena, Seeman, Tomas, Fencl, Filip, Blahova, Kveta, Hojny, Jan, Elisakova, Veronika, Reiterova, Jana, Stekrova, Jitka

“…Cystic kidney diseases are a very heterogeneous group of chronic kidney diseases. The diagnosis is usually based on clinical and ultrasound characteristics and…”
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Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertension by Seeman, Tomáš, Bláhová, Kveta, Fencl, Filip, Klaus, Richard, Lange-Sperandio, Bärbel, Hrčková, Gabriela, Podracká, Ĺudmila

“…Background Impaired kidney concentration capacity is present in half of the patients with autosomal dominant polycystic kidney disease (ADPKD). The kidney…”
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Ophthalmological Aspects of Pierson Syndrome by 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

“…Purpose To study the ocular phenotype of Pierson syndrome and to increase awareness among ophthalmologists of the diagnostic features of this condition. Design…”
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Blood pressure in children with renal cysts and diabetes syndrome by Seeman, Tomáš, Weigel, Friederike, Blahova, Kveta, Fencl, Filip, Pruhova, Stepanka, Hermes, Katharina, Klaus, Richard, Lange-Sperandio, Bärbel, Grote, Veit, John-Kroegel, Ulrike

“…Cystic kidney diseases such as autosomal recessive or dominant polycystic kidney disease (ARPKD and ADPKD) are associated with high prevalence of arterial…”
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Attack of the clones: whole genome-based characterization of two closely related enterohemorrhagic Escherichia coli O26 epidemic lineages by Karnisova, Lucia, Marejkova, Monika, Hrbackova, Hana, Mellmann, Alexander, Karch, Helge, Fruth, Angelika, Drevinek, Pavel, Blahova, Kveta, Bielaszewska, Martina, Nunvar, Jaroslav

“…Enterohemorrhagic Escherichia coli (EHEC) O26:H11/H , the most common non-O157 serotype causing hemolytic uremic syndrome worldwide, are evolutionarily highly…”
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Genotype–phenotype correlation in children with autosomal dominant polycystic kidney disease by Fencl, Filip, Janda, Jan, Bláhová, Květa, Hříbal, Zdeněk, Štekrová, Jitka, Puchmajerová, Alena, Seeman, Tomáš

“…Adults with autosomal dominant polycystic kidney disease (ADPKD) and PKD1 mutations have a more severe disease than do patients with PKD2 mutations. The aim of…”
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Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome by Fencl, Filip, Malina, Michal, Stará, Veronika, Zieg, Jakub, Mixová, Dana, Seeman, Tomáš, Bláhová, Květa

“…Congenital nephrotic syndrome (CNS) is a heterogeneous group of diseases with different causes and prognoses. Two thirds of cases of NS in the first year of…”
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Fatal case of diarrhea-associated hemolytic uremic syndrome with severe neurologic involvement by 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 by SEEMAN, Tomas, JOHN, Ulrike, BLAHOVA, Kveta, VONDRICHOVA, Hana, JANDA, Jan, MISSELWITZ, Joachim

“…Multicystic dysplastic kidney (MCDK) is one of the most common congenital renal anomalies. Arterial hypertension is a potential complication of MCDK. Blood…”
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Long-term follow-up of Czech children with D+ hemolytic-uremic syndrome by BLAHOVA, Kveta, JANDA, Jan, KREISINGER, Jiri, MATEJKOVA, Eva, SEDIVA, Anna

“…Fifty-seven children (f/m=31/26) who survived diarrhea (D) + hemolytic uremic syndrome (HUS) were evaluated. The examinations were performed 1-27 years (median…”
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Complement activation is associated with more severe course of diarrhea-associated hemolytic uremic syndrome, a preliminary study by Karnisova, Lucia, Hradsky, Ondrej, Blahova, Kveta, Fencl, Filip, Dolezel, Zdenek, Zaoral, Tomas, Zieg, Jakub

“…Diarrhea-associated hemolytic uremic syndrome is characterized by hemolytic anemia, thrombocytopenia, and acute kidney injury secondary to enteric infection,…”
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Enterohemorrhagic Escherichia coli as causes of hemolytic uremic syndrome in the Czech Republic by Marejková, Monika, Bláhová, Květa, Janda, Jan, Fruth, Angelika, Petráš, Petr

“…Enterohemorrhagic Escherichia coli (EHEC) cause diarrhea-associated hemolytic uremic syndrome (D+ HUS) worldwide, but no systematic study of EHEC as the…”
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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 by BIELASZEWSKA, M, SCHMIDT, H, LIESEGANG, A, PRAGER, R, RABSCH, W, TSCHÄPE, H, CIZEK, A, JANDA, J, BLAHOVA, K, KARCH, H

“…Article Usage Stats Services JCM Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Mutations in the human laminin β2 (LAMB2) gene and the associated phenotypic spectrum by 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

“…Mutations of LAMB2 typically cause autosomal recessive Pierson syndrome, a disorder characterized by congenital nephrotic syndrome, ocular and neurologic…”
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Urinary transforming growth factor-β1 in children with obstructive uropathy by ZIEG, JAKUB, BLAHOVA, KVETA, SEEMAN, TOMAS, BRONSKY, JIRI, DVORAKOVA, HANA, PECHOVA, MARTA, JANDA, JAN, MATOUSOVIC, KAREL

“…Aim:  Obstructive uropathies (OU) in childhood constitute one of the major causes of chronic renal insufficiency. Transforming growth factor‐β1 (TGF‐β1) is…”
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Various phenotypes of disease associated with mutated DGKE gene by Bezdíčka, Martin, Pavlíček, Petr, Bláhová, Květa, Háček, Jaromír, Zieg, Jakub

“…Atypical haemolytic uraemic syndrome and steroid-resistant nephrotic syndrome are highly rare kidney diseases that can occur in childhood. In some cases,…”
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Severe hypercalcemic crisis in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 gene by Fencl, Filip, Bláhová, Květa, Schlingmann, Karl Peter, Konrad, Martin, Seeman, Tomáš

“…We report on a male infant presenting at 4 months of age with failure to thrive, dehydration, hypotonia, lethargy, and vomiting. Laboratory and imaging tests…”
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Enterohemorrhagic Escherichia coli as Causes of Hemolytic Uremic Syndrome in the Czech Republic: e73927 by Marejkova, Monika, Blahova, Kveta, Janda, Jan, Fruth, Angelika, Petras, Petr

“…Background Enterohemorrhagic Escherichia coli (EHEC) cause diarrhea-associated hemolytic uremic syndrome (D+ HUS) worldwide, but no systematic study of EHEC as…”
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