Search Results - "Oosterveld, Michiel J. S"

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    Compensatory growth of congenital solitary kidneys in pigs reflects increased nephron numbers rather than hypertrophy by van Vuuren, Stefan H, Sol, Chalana M, Broekhuizen, Roel, Lilien, Marc R, Oosterveld, Michiel J S, Nguyen, Tri Q, Goldschmeding, Roel, de Jong, Tom P V M

    Published in PloS one (21-11-2012)
    “…Patients with unilateral MultiCystic Kidney Dysplasia (MCKD) or unilateral renal agenesis (URA) have a congenital solitary functioning kidney (CSFK) that is…”
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    Journal Article
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    Transplantation outcomes in patients with primary hyperoxaluria: a systematic review by Metry, Elisabeth L., van Dijk, Liza M. M., Peters-Sengers, Hessel, Oosterveld, Michiel J.S., Groothoff, Jaap W., Ploeg, Rutger J., Stel, Vianda S., Garrelfs, Sander F.

    Published in Pediatric nephrology (Berlin, West) (01-08-2021)
    “…Background Primary hyperoxaluria type 1 (PH1) is characterized by hepatic overproduction of oxalate and often results in kidney failure. Liver-kidney…”
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    Positive neonatal screening for cystic fibrosis in neonates with renal failure by Oosterveld, Michiel J S, Schilperoort, Jaap V, Lilien, Marc R, Arets, Hubertus G M

    Published in Thorax (01-07-2010)
    “…Screening for cystic fibrosis (CF) was recently added to the neonatal screening programme in the Netherlands. Four patients with renal failure whose heel prick…”
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    Endogenous Oxalate Production in Primary Hyperoxaluria Type 1 Patients by Garrelfs, Sander F, van Harskamp, Dewi, Peters-Sengers, Hessel, van den Akker, Chris H P, Wanders, Ronald J A, Wijburg, Frits A, van Goudoever, Johannes B, Groothoff, Jaap W, Schierbeek, Henk, Oosterveld, Michiel J S

    “…Primary hyperoxaluria type 1 (PH1) is an inborn error of glyoxylate metabolism, characterized by increased endogenous oxalate production. The metabolic…”
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    Nutritional support in 111 pediatric intensive care units: a European survey by VAN DER KUIP, Martijn, OOSTERVELD, Michiel J. S, VAN DER SCHUEREN, Marian A. E. Van Bokhorst-De, DE MEER, K, LAFEBER, Harry N, GEMKE, Reinoud J. B. J

    Published in Intensive care medicine (01-09-2004)
    “…To study current strategies in nutritional management of pediatric intensive care units (PICUs) in Europe, focusing on energy requirements. Survey by a 35-item…”
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    Eculizumab in Pediatric Dense Deposit Disease by Oosterveld, Michiel J S, Garrelfs, Mark R, Hoppe, Bernd, Florquin, Sandrine, Roelofs, Joris J T H, van den Heuvel, L P, Amann, Kerstin, Davin, Jean-Claude, Bouts, Antonia H M, Schriemer, Pietrik J, Groothoff, Jaap W

    “…Dense deposit disease (DDD), a subtype of C3 glomerulopathy, is a rare disease affecting mostly children. Treatment options are limited. Debate exists whether…”
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