Folyóiratcikkek tallózása szerző szerint "Kerti, Andrea"

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  • Ambulatory arterial stiffness index in children after kidney transplantation 
    Dégi, Arianna Amália; Kerti, Andrea; Cseprekál, Orsolya; Kis, Éva PhD; Sallay, Péter; Szabó, Attila; Reusz, György (2013)
    Given the increase in CV morbidity after RTx and the scarcity of CV events in pediatrics, surrogate markers should be assessed to characterize CV damage in this population. AASI is a marker of arterial stiffness in adults, ...
  • A szteroid-rezisztens nephrosis szindróma genetikai vizsgálata Magyarországon 
    Kerti, Andrea; Jávorszky, Eszter; Csohány, Rózsa; Varga, Noémi-Ágnes; Szabó, Attila; Árkossy, Ottó; Sallay, Péter; Balogh, Lídia; Szabó, Tamás; Reusz, György; Tulassay, Tivadar; Tory, Kálmán (2013)
    Bevezetés: A szteroid-rezisztens nephrosis szindróma egy rossz prognózisú kórkép. Immunológiai és monogénes formájának elkülönítése fontos, mert kezelésük különböző, de rendszerint csak genetikai vizsgálattal lehet ...
  • Az ambuláns artériás stiffness index (AASI) vizsgálata vesetranszplantált gyermekek esetében 
    Dégi, Arianna Amália; Kerti, Andrea; Kis, Éva PhD; Cseprekál, Orsolya; Reusz, György (2011)
  • Az izolált szteroid-rezisztens nephrosis szindróma genetikája - az ezredfordulót övező két évtized eredményei 
    Tory, Kálmán; Kerti, Andrea; Reusz, György (2011)
  • Bone Metabolism and Arterial Stiffness After Renal Transplantation 
    Cseprekál, Orsolya; Kis, Éva PhD; Dégi, Arianna Amália; Kerti, Andrea; Szabó, Attila; Reusz, György (2014)
    <b><i>Background/Aims: </i></b>To assess the relationship between bone and vascular disease and its changes over time after renal transplantation. Metabolic bone disease (MBD) is common in chronic kidney disease (CKD) and ...
  • Cardiovascular risk assessment in children with chronic kidney disease 
    Shroff R; Dégi, Arianna Amália; Kerti, Andrea; Kis, Éva PhD; Cseprekál, Orsolya; Tory, Kálmán; Szabó, Attila; Reusz, György (2013)
    Chronic kidney disease (CKD) is a major factor contributing to cardiovascular (CV) morbidity and mortality with the highest risk in patients on dialysis. An estimation of CV risk is important not only to identify ...
  • Measurement of pulse wave velocity in children and young adults: a comparative study using three different devices 
    Kis, Éva PhD; Cseprekál, Orsolya; Kerti, Andrea; Salvi P; Benetos A; Tislér, András; Szabó, Attila; Tulassay, Tivadar; Reusz, György (2011)
    To estimate the value of pulse wave velocity (PWV) in pediatric cardiovascular disease, prospective studies are needed. Various instruments based on different measurement principles are proposed for use in children, ...
  • Mutation-dependent recessive inheritance of NPHS2-associated steroid-resistant nephrotic syndrome 
    Tory, Kálmán; Karancsiné Menyhárd, Dóra; Woerner S; Nevo F; Gribouval O; Kerti, Andrea; Straner P; Arrondel C; Cong EH; Tulassay, Tivadar; Mollet G; Perczel, András; Antignac C (2014)
    Monogenic disorders result from defects in a single gene. According to Mendel's laws, these disorders are inherited in either a recessive or dominant fashion. Autosomal-recessive disorders require a disease-causing variant ...
  • NPHS2 homozygous p.R229Q variant: potential modifier instead of causal effect in focal segmental glomerulosclerosis 
    Kerti, Andrea; Csohány, Rózsa; Wágner, László József; Jávorszky, Eszter; Maka, Erika; Tory, Kálmán (2013)
    BACKGROUND: The pathogenicity of the NPHS2 homozygous p.R229Q variant in steroid-resistant nephrotic syndrome (SRNS) is doubtful. While it has been reported in unaffected controls, it is enriched in patients with SRNS, ...
  • 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 of obesity and metabolic changes after kidney transplantation: hungarian pediatric cohort study 
    Dégi, Arianna Amália; Kis, Éva PhD; Kerti, Andrea; Cseprekál, Orsolya; Szabó, Attila; Reusz, György (2014)
    BACKGROUND: Cardiovascular mortality rate in patients with end-stage renal disease is 3 magnitudes higher than in the general population; it remains 10-fold higher after successful renal transplantation (Tx). Among others, ...
  • Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis 
    Balogh, Eszter; Chandler, Jennifer C.; Varga, Máté; Tahoun, Mona; Menyhárd, Dóra K.; Schay, Gusztáv; Goncalves, Tomas; Hamar, Renáta; Légrádi, Regina; Szekeres, Ákos; Gribouval, Olivier; Kleta, Robert; Stanescu, Horia; Bockenhauer, Detlef; Kerti, Andrea; Williams, Hywel; Kinsler, Veronica; Di, Wei-Li; Curtis, David; Kolatsi-Joannou, Maria; Hammid, Hafsa; Szőcs, Anna; Perczel, Kristóf; Maka, Erika; Toldi, Gergely; Sava, Florentina; Arrondel, Christelle; Kardos, Magdolna; Fintha, Attila; Hossain, Ahmed; D’Arco, Felipe; Kaliakatsos, Mario; Koeglmeier, Jutta; Mifsud, William; Moosajee, Mariya; Faro, Ana; Jávorszky, Eszter; Rudas, Gábor; Saied, Marwa H.; Marzouk, Salah; Kelen, Kata; Götze, Judit; Reusz, George; Tulassay, Tivadar; Dragon, François; Mollet, Géraldine; Motameny, Susanne; Thiele, Holger; Dorval, Guillaume; Nürnberg, Peter; Perczel, András; Szabó, Attila J.; Long, David A.; Tomita, Kazunori; Antignac, Corinne; Waters, Aoife M.; Tory, Kálmán (2020)
  • QMPSF is sensitive and specific in the detection of NPHP1 heterozygous deletions 
    Jávorszky, Eszter; Moriniere V; Kerti, Andrea; Balogh, Eszter; Piko H; Saunier S; Karcagi V; Antignac C; Tory, Kálmán (2017)
    BACKGROUND: Nephronophthisis, an autosomal recessive nephropathy, is responsible for 10% of childhood chronic renal failure. The deletion of its major gene, NPHP1, with a minor allele frequency of 0.24% in the general ...