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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1989 1
1990 2
1991 4
1992 5
1993 3
1994 2
1995 3
1996 4
1997 5
1998 10
1999 10
2000 6
2001 6
2002 3
2003 2
2004 3
2005 7
2006 7
2007 5
2008 4
2009 1
2010 6
2011 7
2012 9
2013 11
2014 4
2015 3
2016 2
2017 3
2018 3
2019 3
2020 7
2021 7
2022 2
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142 results
Results by year
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Page 1
Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle.
Knottnerus SJG, Bleeker JC, Wüst RCI, Ferdinandusse S, IJlst L, Wijburg FA, Wanders RJA, Visser G, Houtkooper RH. Knottnerus SJG, et al. Among authors: ijlst l. Rev Endocr Metab Disord. 2018 Mar;19(1):93-106. doi: 10.1007/s11154-018-9448-1. Rev Endocr Metab Disord. 2018. PMID: 29926323 Free PMC article. Review.
Peroxisomal Metabolite and Cofactor Transport in Humans.
Chornyi S, IJlst L, van Roermund CWT, Wanders RJA, Waterham HR. Chornyi S, et al. Among authors: ijlst l. Front Cell Dev Biol. 2021 Jan 11;8:613892. doi: 10.3389/fcell.2020.613892. eCollection 2020. Front Cell Dev Biol. 2021. PMID: 33505966 Free PMC article. Review.
Metabolite transport across the peroxisomal membrane.
Visser WF, van Roermund CW, Ijlst L, Waterham HR, Wanders RJ. Visser WF, et al. Among authors: ijlst l. Biochem J. 2007 Jan 15;401(2):365-75. doi: 10.1042/BJ20061352. Biochem J. 2007. PMID: 17173541 Free PMC article. Review.
Fatty acid metabolism in Saccharomyces cerevisiae.
van Roermund CW, Waterham HR, Ijlst L, Wanders RJ. van Roermund CW, et al. Among authors: ijlst l. Cell Mol Life Sci. 2003 Sep;60(9):1838-51. doi: 10.1007/s00018-003-3076-x. Cell Mol Life Sci. 2003. PMID: 14523547 Review.
Exploring the metabolic fate of medium-chain triglycerides in healthy individuals using a stable isotope tracer.
Knottnerus SJG, van Harskamp D, Schierbeek H, Bleeker JC, Crefcoeur LL, Ferdinandusse S, van Goudoever JB, Houtkooper RH, IJlst L, Langeveld M, Wanders RJA, Vaz FM, Wijburg FA, Visser G. Knottnerus SJG, et al. Among authors: ijlst l. Clin Nutr. 2021 Mar;40(3):1396-1404. doi: 10.1016/j.clnu.2020.08.032. Epub 2020 Sep 4. Clin Nutr. 2021. PMID: 32948349
Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Do not Improve with Carnitine Supplementation.
Verkerk AO, Knottnerus SJG, Portero V, Bleeker JC, Ferdinandusse S, Guan K, IJlst L, Visser G, Wanders RJA, Wijburg FA, Bezzina CR, Mengarelli I, Houtkooper RH. Verkerk AO, et al. Among authors: ijlst l. Front Pharmacol. 2021 Jan 12;11:616834. doi: 10.3389/fphar.2020.616834. eCollection 2020. Front Pharmacol. 2021. PMID: 33597881 Free PMC article.
Disorders of mitochondrial fatty acyl-CoA beta-oxidation.
Wanders RJ, Vreken P, den Boer ME, Wijburg FA, van Gennip AH, IJlst L. Wanders RJ, et al. Among authors: ijlst l. J Inherit Metab Dis. 1999 Jun;22(4):442-87. doi: 10.1023/a:1005504223140. J Inherit Metab Dis. 1999. PMID: 10407780 Review.
An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids.
Ferdinandusse S, McWalter K, Te Brinke H, IJlst L, Mooijer PM, Ruiter JPN, van Lint AEM, Pras-Raves M, Wever E, Millan F, Guillen Sacoto MJ, Begtrup A, Tarnopolsky M, Brady L, Ladda RL, Sell SL, Nowak CB, Douglas J, Tian C, Ulm E, Perlman S, Drack AV, Chong K, Martin N, Brault J, Brokamp E, Toro C, Gahl WA, Macnamara EF, Wolfe L; Undiagnosed Diseases Network, Waisfisz Q, Zwijnenburg PJG, Ziegler A, Barth M, Smith R, Ellingwood S, Gaebler-Spira D, Bakhtiari S, Kruer MC, van Kampen AHC, Wanders RJA, Waterham HR, Cassiman D, Vaz FM. Ferdinandusse S, et al. Among authors: ijlst l. Genet Med. 2021 Apr;23(4):740-750. doi: 10.1038/s41436-020-01027-3. Epub 2020 Nov 26. Genet Med. 2021. PMID: 33239752 Free PMC article.
Prediction of phenotypic severity in mucopolysaccharidosis type IIIA.
Knottnerus SJG, Nijmeijer SCM, IJlst L, Te Brinke H, van Vlies N, Wijburg FA. Knottnerus SJG, et al. Among authors: ijlst l. Ann Neurol. 2017 Nov;82(5):686-696. doi: 10.1002/ana.25069. Epub 2017 Oct 26. Ann Neurol. 2017. PMID: 29023963 Free PMC article.
142 results