tallózása szerző szerint "Schaefer F"

A találatok rendezése: Rendezés: Találatok:

  • Adult Height in Patients with Advanced CKD Requiring Renal Replacement Therapy during Childhood. 
    Harambat J; Bonthuis M; van Stralen KJ; Ariceta G; Battelino N; Bjerre A; Jahnukainen T; Leroy V; Reusz, György; Sandes AR; Sinha MD; Groothoff JW; Combe C; Jager KJ; Verrina E; Schaefer F; ESPN/ERA-EDTA Registry (2014)
    BACKGROUND AND OBJECTIVES: Growth and final height are of major concern in children with ESRD. This study sought to describe the distribution of adult height of patients who started renal replacement therapy (RRT) during ...
  • Anemia in children following renal transplantation-results from the ESPN/ERA-EDTA Registry 
    Krischock LA; van Stralen KJ; Verrina E; Tizard EJ; Bonthuis M; Reusz, György; Hussain FK; Jankauskiene A; Novljan G; Spasojevic-Dimitrijeva B; Podracka L; Zaller V; Jager KJ; Schaefer F; ESPN/ERA-EDTA Registry (2016)
    BACKGROUND: Our aim was to determine the prevalence of sub-target hemoglobin (Hb) levels in children with a renal allograft and to identify potential determinants associated with these Hb levels. METHODS: Data from 3669 ...
  • Considerable variations in growth hormone policy and prescription in paediatric end-stage renal disease across European countries-a report from the ESPN/ERA-EDTA registry. 
    van Huis M; Bonthuis M; Sahpazova E; Mencarelli F; Spasojevic B; Reusz, György; Caldas-Afonso A; Bjerre A; Baiko S; Vondrak K; Molchanova EA; Kolvek G; Zaikova N; Bohm M; Ariceta G; Jager KJ; Schaefer F; van Stralen KJ; Groothoff JW (2016)
    BACKGROUND: Growth retardation in paediatric end-stage renal disease (ESRD) has a serious impact on adult life. It is potentially treatable with recombinant growth hormone (rGH). In this study, we aimed to quantify the ...
  • Development of the circadian clockwork in the kidney. 
    Mészáros, Krisztina; Pruess L; Szabó, Attila; Gondan M; Ritz E; Schaefer F (2014)
    The circadian molecular clock is an internal time-keeping system composed of centrally synchronized tissue-level pacemakers. Here, we explored the ontogeny of the clock machinery in the developing kidney. Pregnant rats ...
  • Genotype-phenotype associations in WT1 glomerulopathy 
    Lipska BS; Ranchin B; Iatropoulos P; Gellermann J; Melk A; Ozaltin F; Caridi G; Seeman T; Tory, Kálmán; Jankauskiene A; Zurowska A; Szczepanska M; Wasilewska A; Harambat J; Trautmann A; Peco-Antic A; Borzecka H; Moczulska A; Saeed B; Bogdanovic R; Kalyoncu M; Simkova E; Erdogan O; Vrljicak K; Teixeira A; Azocar M; Schaefer F; PodoNet Consortium (2014)
    WT1 mutations cause a wide spectrum of renal and extrarenal manifestations. Here we evaluated disease prevalence, phenotype spectrum, and genotype-phenotype correlations of 61 patients with WT1-related steroid-resistant ...
  • Normal 25-Hydroxyvitamin D Levels Are Associated with Less Proteinuria and Attenuate Renal Failure Progression in Children with CKD 
    Shroff R; Aitkenhead H; Costa N; Trivelli A; Litwin M; Picca S; Anarat A; Sallay, Péter; Ozaltin F; Zurowska A; Jankauskiene A; Montini G; Charbit M; Schaefer F; Wuhl E; ESCAPE Trial Group (2016)
    Angiotensin-converting enzyme inhibitors (ACEi) for renin-angiotensin-aldosterone system (RAAS) blockade are routinely used to slow CKD progression. However, vitamin D may also promote renoprotection by suppressing renin ...
  • NPHS2 p.V290M mutation in late-onset steroid-resistant nephrotic syndrome. 
    Kerti, Andrea; Csohány, Rózsa; Szabó, Attila; Arkossy O; Sallay, Péter; Moriniere V; Vega-Warner V; Nyírő, Gábor; Lakatos, Orsolya Judit; Szabó, Tamás; Lipska BS; Schaefer F; Antignac C; Reusz, György; Tulassay, Tivadar; Tory, Kálmán (2013)
    BACKGROUND: The most frequently mutated gene of steroid- resistant nephrotic syndrome (SRNS) is NPHS2. Current guidelines propose the sequencing of all NPHS2 exons only in childhood- onset SRNS. METHODS: A cohort of ...
  • Prevalence and predictors of the sub-target Hb level in children on dialysis 
    Van Stralen KJ; Krischock L; Schaefer F; Verrina E; Groothoff JW; Evans J; Heaf J; Ivanov D; Kostic M; Maringhini S; Podracká L; Printza N; Pundziene B; Reusz, György; Vondrak K; Jager KJ; Jane Tizard E; on behalf of the ESPN/ERA-EDTA Registry (2012)
    BackgroundAnaemia is a common and potentially treatable co-morbidity of end-stage renal disease. We aimed to determine the prevalence of the sub-target haemoglobin (Hb) level among European children on dialysis and to ...
  • Quantitative Histomorphometry of the Healthy Peritoneum 
    Schaefer B; Bartosova M; MacHer-Goeppinger S; Ujszászi, Ákos; Wallwiener M; Nyarangi-Dix J; Sallay, Péter; Burkhardt D; Querfeld U; Pfeifle V; Lahrmann B; Schwenger V; Wühl E; Holland-Cunz S; Schaefer F; Schmitt CP (2016)
    The peritoneum plays an essential role in preventing abdominal frictions and adhesions and can be utilized as a dialysis membrane. Its physiological ultrastructure, however, has not yet been studied systematically. 106 ...
  • The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase epsilon 
    Azukaitis K; Simkova E; Majid MA; Galiano M; Benz K; Amann K; Bockmeyer C; Gajjar R; Meyers KE; Cheong HI; Lange-Sperandio B; Jungraithmayr T; Fremeaux-Bacchi V; Bergmann C; Bereczki, Csaba; Miklaszewska M; Csuka, Dorottya; Prohászka, Zoltán; Gipson P; Sampson MG; Lemaire M; Schaefer F (2017)
    The recent discovery of mutations in the gene encoding diacylglycerol kinase epsilon (DGKE) identified a novel pathophysiologic mechanism leading to HUS and/or MPGN. We report ten new patients from eight unrelated kindreds ...