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Long-term outcome after cyclophosphamide treatment in children with steroid-dependent and frequently relapsing minimal change nephrotic syndrome.
Am J Kidney Dis. 2007 May;49(5):592-7. doi: 10.1053/j.ajkd.2007.02.270.
Am J Kidney Dis. 2007.
PMID: 17472840
Long-term outcome of biopsy-proven, frequently relapsing minimal-change nephrotic syndrome in children.
Kyrieleis HA, Löwik MM, Pronk I, Cruysberg HR, Kremer JA, Oyen WJ, van den Heuvel BL, Wetzels JF, Levtchenko EN.
Kyrieleis HA, et al.
Clin J Am Soc Nephrol. 2009 Oct;4(10):1593-600. doi: 10.2215/CJN.05691108. Epub 2009 Sep 24.
Clin J Am Soc Nephrol. 2009.
PMID: 19808243
Free PMC article.
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[Pneumatosis intestinalis in 9 children with an oncologic disease].
Kyrieleis HA, Wilsterman ME, Severijnen RS, van Die CE, Bongaerts GP, Gidding CE.
Kyrieleis HA, et al.
Ned Tijdschr Geneeskd. 2005 Mar 19;149(12):647-52.
Ned Tijdschr Geneeskd. 2005.
PMID: 15813432
Dutch.
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Phase 1/2 Study of Lumasiran for Treatment of Primary Hyperoxaluria Type 1: A Placebo-Controlled Randomized Clinical Trial.
Frishberg Y, Deschênes G, Groothoff JW, Hulton SA, Magen D, Harambat J, Van't Hoff WG, Lorch U, Milliner DS, Lieske JC, Haslett P, Garg PP, Vaishnaw AK, Talamudupula S, Lu J, Habtemariam BA, Erbe DV, McGregor TL, Cochat P; study collaborators.
Frishberg Y, et al.
Clin J Am Soc Nephrol. 2021 Jul;16(7):1025-1036. doi: 10.2215/CJN.14730920. Epub 2021 May 13.
Clin J Am Soc Nephrol. 2021.
PMID: 33985991
Free PMC article.
Clinical Trial.
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FAT1 mutations cause a glomerulotubular nephropathy.
Gee HY, Sadowski CE, Aggarwal PK, Porath JD, Yakulov TA, Schueler M, Lovric S, Ashraf S, Braun DA, Halbritter J, Fang H, Airik R, Vega-Warner V, Cho KJ, Chan TA, Morris LG, ffrench-Constant C, Allen N, McNeill H, Büscher R, Kyrieleis H, Wallot M, Gaspert A, Kistler T, Milford DV, Saleem MA, Keng WT, Alexander SI, Valentini RP, Licht C, Teh JC, Bogdanovic R, Koziell A, Bierzynska A, Soliman NA, Otto EA, Lifton RP, Holzman LB, Sibinga NE, Walz G, Tufro A, Hildebrandt F.
Gee HY, et al.
Nat Commun. 2016 Feb 24;7:10822. doi: 10.1038/ncomms10822.
Nat Commun. 2016.
PMID: 26905694
Free PMC article.
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Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly.
Lahrouchi N, George A, Ratbi I, Schneider R, Elalaoui SC, Moosa S, Bharti S, Sharma R, Abu-Asab M, Onojafe F, Adadi N, Lodder EM, Laarabi FZ, Lamsyah Y, Elorch H, Chebbar I, Postma AV, Lougaris V, Plebani A, Altmueller J, Kyrieleis H, Meiner V, McNeill H, Bharti K, Lyonnet S, Wollnik B, Henrion-Caude A, Berraho A, Hildebrandt F, Bezzina CR, Brooks BP, Sefiani A.
Lahrouchi N, et al.
Nat Commun. 2019 Mar 12;10(1):1180. doi: 10.1038/s41467-019-08547-w.
Nat Commun. 2019.
PMID: 30862798
Free PMC article.
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Targeted therapy with eculizumab for inherited CD59 deficiency.
Höchsmann B, Dohna-Schwake C, Kyrieleis HA, Pannicke U, Schrezenmeier H.
Höchsmann B, et al. Among authors: kyrieleis ha.
N Engl J Med. 2014 Jan 2;370(1):90-2. doi: 10.1056/NEJMc1308104.
N Engl J Med. 2014.
PMID: 24382084
No abstract available.
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