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Page 1
Cardiovascular risk assessment in children with chronic kidney disease.
Shroff R, Dégi A, Kerti A, Kis E, Cseprekál O, Tory K, Szabó AJ, Reusz GS. Shroff R, et al. Among authors: tory k. Pediatr Nephrol. 2013 Jun;28(6):875-84. doi: 10.1007/s00467-012-2325-3. Epub 2012 Oct 16. Pediatr Nephrol. 2013. PMID: 23070276 Review.
Monitoring cardiovascular changes during hemodialysis in children.
Miltényi G, Tory K, Stubnya G, Tóth-Heyn P, Vásárhelyi B, Sallay P, Szabó A, Tulassay T, Dobos M, Reusz GS. Miltényi G, et al. Among authors: tory k. Pediatr Nephrol. 2001 Jan;16(1):19-24. doi: 10.1007/s004670000497. Pediatr Nephrol. 2001. PMID: 11198597
Signs of autonomic neuropathy in childhood uremia.
Tory K, Sallay P, Tóth-Heyn P, Szabó A, Szabó A, Tulassay T, Reusz GS. Tory K, et al. Pediatr Nephrol. 2001 Jan;16(1):25-8. doi: 10.1007/s004670000484. Pediatr Nephrol. 2001. PMID: 11198598
Autonomic dysfunction in uremia assessed by heart rate variability.
Tory K, Süveges Z, Horváth E, Bokor E, Sallay P, Berta K, Szabó A, Tulassay T, Reusz GS. Tory K, et al. Pediatr Nephrol. 2003 Nov;18(11):1167-71. doi: 10.1007/s00467-003-1280-4. Epub 2003 Sep 17. Pediatr Nephrol. 2003. PMID: 13680330
NPHS2 p.V290M mutation in late-onset steroid-resistant nephrotic syndrome.
Kerti A, Csohány R, Szabó A, Arkossy O, Sallay P, Moriniére V, Vega-Warner V, Nyírő G, Lakatos O, Szabó T, Lipska BS, Schaefer F, Antignac C, Reusz G, Tulassay T, Tory K. Kerti A, et al. Among authors: tory k. Pediatr Nephrol. 2013 May;28(5):751-7. doi: 10.1007/s00467-012-2379-2. Epub 2012 Dec 14. Pediatr Nephrol. 2013. PMID: 23242530
Comprehensive genetic testing in children with a clinical diagnosis of ARPKD identifies phenocopies.
Szabó T, Orosz P, Balogh E, Jávorszky E, Máttyus I, Bereczki C, Maróti Z, Kalmár T, Szabó AJ, Reusz G, Várkonyi I, Marián E, Gombos É, Orosz O, Madar L, Balla G, Kappelmayer J, Tory K, Balogh I. Szabó T, et al. Among authors: tory k. Pediatr Nephrol. 2018 Oct;33(10):1713-1721. doi: 10.1007/s00467-018-3992-5. Epub 2018 Jun 28. Pediatr Nephrol. 2018. PMID: 29956005
Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis.
Balogh E, Chandler JC, Varga M, Tahoun M, Menyhárd DK, Schay G, Goncalves T, Hamar R, Légrádi R, Szekeres Á, Gribouval O, Kleta R, Stanescu H, Bockenhauer D, Kerti A, Williams H, Kinsler V, Di WL, Curtis D, Kolatsi-Joannou M, Hammid H, Szőcs A, Perczel K, Maka E, Toldi G, Sava F, Arrondel C, Kardos M, Fintha A, Hossain A, D'Arco F, Kaliakatsos M, Koeglmeier J, Mifsud W, Moosajee M, Faro A, Jávorszky E, Rudas G, Saied MH, Marzouk S, Kelen K, Götze J, Reusz G, Tulassay T, Dragon F, Mollet G, Motameny S, Thiele H, Dorval G, Nürnberg P, Perczel A, Szabó AJ, Long DA, Tomita K, Antignac C, Waters AM, Tory K. Balogh E, et al. Among authors: tory k. Proc Natl Acad Sci U S A. 2020 Jun 30;117(26):15137-15147. doi: 10.1073/pnas.2002328117. Epub 2020 Jun 17. Proc Natl Acad Sci U S A. 2020. PMID: 32554502 Free PMC article.
109 results