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Journal Abstract Search

311 related items for PubMed ID: 27761660

  • 1. Timing of renal replacement therapy does not influence survival and growth in children with congenital nephrotic syndrome caused by mutations in NPHS1: data from the ESPN/ERA-EDTA Registry.
    Hölttä T, Bonthuis M, Van Stralen KJ, Bjerre A, Topaloglu R, Ozaltin F, Holmberg C, Harambat J, Jager KJ, Schaefer F, Groothoff JW.
    Pediatr Nephrol; 2016 Dec; 31(12):2317-2325. PubMed ID: 27761660
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  • 2. Outcomes of renal replacement therapy in boys with prune belly syndrome: findings from the ESPN/ERA-EDTA Registry.
    Yalcinkaya F, Bonthuis M, Erdogan BD, van Stralen KJ, Baiko S, Chehade H, Maxwell H, Montini G, Rönnholm K, Sørensen SS, Ulinski T, Verrina E, Weber S, Harambat J, Schaefer F, Jager KJ, Groothoff JW.
    Pediatr Nephrol; 2018 Jan; 33(1):117-124. PubMed ID: 28779237
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  • 3. Plasma exchange and retransplantation in recurrent nephrosis of patients with congenital nephrotic syndrome of the Finnish type (NPHS1).
    Kuusniemi AM, Qvist E, Sun Y, Patrakka J, Rönnholm K, Karikoski R, Jalanko H.
    Transplantation; 2007 May 27; 83(10):1316-23. PubMed ID: 17519780
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  • 4. Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients.
    Patrakka J, Kestilä M, Wartiovaara J, Ruotsalainen V, Tissari P, Lenkkeri U, Männikkö M, Visapää I, Holmberg C, Rapola J, Tryggvason K, Jalanko H.
    Kidney Int; 2000 Sep 27; 58(3):972-80. PubMed ID: 10972661
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  • 5. Characteristics and Outcomes of Patients With Systemic Sclerosis (Scleroderma) Requiring Renal Replacement Therapy in Europe: Results From the ERA-EDTA Registry.
    Hruskova Z, Pippias M, Stel VS, Abad-Díez JM, Benítez Sánchez M, Caskey FJ, Collart F, De Meester J, Finne P, Heaf JG, Magaz A, Palsson R, Reisæter AV, Salama AD, Segelmark M, Traynor JP, Massy ZA, Jager KJ, Tesar V.
    Am J Kidney Dis; 2019 Feb 27; 73(2):184-193. PubMed ID: 30122544
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  • 6. Infants Requiring Maintenance Dialysis: Outcomes of Hemodialysis and Peritoneal Dialysis.
    Vidal E, van Stralen KJ, Chesnaye NC, Bonthuis M, Holmberg C, Zurowska A, Trivelli A, Da Silva JEE, Herthelius M, Adams B, Bjerre A, Jankauskiene A, Miteva P, Emirova K, Bayazit AK, Mache CJ, Sánchez-Moreno A, Harambat J, Groothoff JW, Jager KJ, Schaefer F, Verrina E, ESPN/ERA-EDTA Registry.
    Am J Kidney Dis; 2017 May 27; 69(5):617-625. PubMed ID: 27955924
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  • 8. Improvement in the renal prognosis in nephropathic cystinosis.
    Van Stralen KJ, Emma F, Jager KJ, Verrina E, Schaefer F, Laube GF, Lewis MA, Levtchenko EN.
    Clin J Am Soc Nephrol; 2011 Oct 27; 6(10):2485-91. PubMed ID: 21868618
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  • 15. Congenital nephrotic syndrome with a novel NPHS1 mutation.
    Yoshizawa C, Kobayashi Y, Ikeuchi Y, Tashiro M, Kakegawa S, Watanabe T, Goto Y, Nakanishi K, Yoshikawa N, Arakawa H.
    Pediatr Int; 2016 Nov 27; 58(11):1211-1215. PubMed ID: 27882743
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  • 17. Management of children with congenital nephrotic syndrome: challenging treatment paradigms.
    Dufek S, Holtta T, Trautmann A, Ylinen E, Alpay H, Ariceta G, Aufricht C, Bacchetta J, Bakkaloglu SA, Bayazit A, Cicek RY, Dursun I, Duzova A, Ekim M, Iancu D, Jankauskiene A, Klaus G, Paglialonga F, Pasini A, Printza N, Said Conti V, do Sameiro Faria M, Schmitt CP, Stefanidis CJ, Verrina E, Vidal E, Vondrak K, Webb H, Zampetoglou A, Bockenhauer D, Edefonti A, Shroff R.
    Nephrol Dial Transplant; 2019 Aug 01; 34(8):1369-1377. PubMed ID: 30215773
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