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Rhabdomyolysis: review of the literature.
Zutt R, van der Kooi AJ, Linthorst GE, Wanders RJ, de Visser M. Zutt R, et al. Among authors: wanders rj. Neuromuscul Disord. 2014 Aug;24(8):651-9. doi: 10.1016/j.nmd.2014.05.005. Epub 2014 May 21. Neuromuscul Disord. 2014. PMID: 24946698 Review.
[Recurrent rhabdomyolysis: screening for underlying disease].
Zutt R, van der Kooi AJ, Linthorst GE, Wanders RJ, Verschuuren JJ, de Visser M. Zutt R, et al. Among authors: wanders rj. Ned Tijdschr Geneeskd. 2010;154:A2290. Ned Tijdschr Geneeskd. 2010. PMID: 21083951 Dutch.
Novel Insights Into Gyrate Atrophy of the Choroid and Retina (GACR): A Cohort Study.
Balfoort BM, Van den Broeck F, Boon CJF, Brouwers MCGJ, Diederen RMH, Dhillon P; GACR “Bird's Eye View” Consortium; van Hasselt PM, Jaeger B, Karuntu JS, Rennings AJM, van Spronsen FJ, Timmer C, Wagenmakers MAEM, De Zaeytijd J, Leroy BP, Schulze A, van Karnebeek CD, Brands MM. Balfoort BM, et al. J Inherit Metab Dis. 2025 Jan;48(1):e12842. doi: 10.1002/jimd.12842. J Inherit Metab Dis. 2025. PMID: 39761806 Free PMC article.
Syndromic Retinitis Pigmentosa.
Karuntu JS, Almushattat H, Nguyen XT, Plomp AS, Wanders RJA, Hoyng CB, van Schooneveld MJ, Schalij-Delfos NE, Brands MM, Leroy BP, van Karnebeek CDM, Bergen AA, van Genderen MM, Boon CJF. Karuntu JS, et al. Among authors: wanders rja. Prog Retin Eye Res. 2024 Dec 27:101324. doi: 10.1016/j.preteyeres.2024.101324. Online ahead of print. Prog Retin Eye Res. 2024. PMID: 39733931 Free article. Review.
Development of the Dutch translational knowledge agenda for inherited metabolic diseases.
Hieltjes IJ, van der Lee JH, Groenendijk MC, van Haaften G, van Hasselt PM, Lunsing RJ, van Prooijen GJJ, de Ruiter EM, van Spronsen FJ, Verhoeven-Duif NM, de Vreugd A, Wagenmakers M, Zweers H, Dekker H, Waterham HR, van Karnebeek CD, Wanders RJA, Wevers RA. Hieltjes IJ, et al. Among authors: wanders rja. JIMD Rep. 2024 Dec 22;66(1):e12455. doi: 10.1002/jmd2.12455. eCollection 2025 Jan. JIMD Rep. 2024. PMID: 39723120 Free PMC article.
A Dutch translational knowledge agenda for inherited metabolic diseases.
Waterham HR, Wanders RJA, Wevers RA, van Karnebeek CD. Waterham HR, et al. Among authors: wanders rja. J Inherit Metab Dis. 2025 Jan;48(1):e12812. doi: 10.1002/jimd.12812. Epub 2024 Nov 16. J Inherit Metab Dis. 2025. PMID: 39548774 No abstract available.
Extending diagnostic practices in gyrate atrophy: Enzymatic characterization and the development of an in vitro pyridoxine responsiveness assay.
Balfoort BM, Pampalone G, Ruiter JPN, Denis SW, Brands MM; GACR Bird's Eye View Consortium; Timmer C, Wagenmakers MAEM, Wanders RJA, van Karnebeek CD, Cellini B, Houtkooper RH, Ferdinandusse S. Balfoort BM, et al. Among authors: wanders rja. Mol Genet Metab. 2024 Sep-Oct;143(1-2):108542. doi: 10.1016/j.ymgme.2024.108542. Epub 2024 Jul 19. Mol Genet Metab. 2024. PMID: 39053126 Free article.
Disorders of fatty acid homeostasis.
Vaz FM, Ferdinandusse S, Salomons GS, Wanders RJA. Vaz FM, et al. Among authors: wanders rja. J Inherit Metab Dis. 2025 Jan;48(1):e12734. doi: 10.1002/jimd.12734. Epub 2024 May 1. J Inherit Metab Dis. 2025. PMID: 38693715 Free PMC article. Review.
1,027 results