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

Year Number of Results
1997 1
1998 1
1999 3
2000 4
2001 3
2002 8
2003 6
2004 4
2005 5
2006 8
2007 6
2008 3
2009 3
2010 5
2011 3
2012 5
2013 3
2014 6
2015 20
2016 18
2017 22
2018 14
2019 9
2020 24
2021 9
2022 12
2023 7
2024 2

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180 results

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Page 1
The physiological functions of human peroxisomes.
Wanders RJA, Baes M, Ribeiro D, Ferdinandusse S, Waterham HR. Wanders RJA, et al. Among authors: ferdinandusse s. Physiol Rev. 2023 Jan 1;103(1):957-1024. doi: 10.1152/physrev.00051.2021. Epub 2022 Aug 11. Physiol Rev. 2023. PMID: 35951481 Free article. Review.
International Recommendations for the Diagnosis and Management of Patients With Adrenoleukodystrophy: A Consensus-Based Approach.
Engelen M, van Ballegoij WJC, Mallack EJ, Van Haren KP, Köhler W, Salsano E, van Trotsenburg ASP, Mochel F, Sevin C, Regelmann MO, Tritos NA, Halper A, Lachmann RH, Davison J, Raymond GV, Lund TC, Orchard PJ, Kuehl JS, Lindemans CA, Caruso P, Turk BR, Moser AB, Vaz FM, Ferdinandusse S, Kemp S, Fatemi A, Eichler FS, Huffnagel IC. Engelen M, et al. Among authors: ferdinandusse s. Neurology. 2022 Nov 22;99(21):940-951. doi: 10.1212/WNL.0000000000201374. Epub 2022 Sep 29. Neurology. 2022. PMID: 36175155 Free PMC article.
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: ferdinandusse s. 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.
Sex-specific newborn screening for X-linked adrenoleukodystrophy.
Albersen M, van der Beek SL, Dijkstra IME, Alders M, Barendsen RW, Bliek J, Boelen A, Ebberink MS, Ferdinandusse S, Goorden SMI, Heijboer AC, Jansen M, Jaspers YRJ, Metgod I, Salomons GS, Vaz FM, Verschoof-Puite RK, Visser WF, Dekkers E, Engelen M, Kemp S. Albersen M, et al. Among authors: ferdinandusse s. J Inherit Metab Dis. 2023 Jan;46(1):116-128. doi: 10.1002/jimd.12571. Epub 2022 Oct 26. J Inherit Metab Dis. 2023. PMID: 36256460 Free PMC article.
Clinical and Laboratory Diagnosis of Peroxisomal Disorders.
Wanders RJ, Klouwer FC, Ferdinandusse S, Waterham HR, Poll-Thé BT. Wanders RJ, et al. Among authors: ferdinandusse s. Methods Mol Biol. 2017;1595:329-342. doi: 10.1007/978-1-4939-6937-1_30. Methods Mol Biol. 2017. PMID: 28409475 Review.
Human disorders of peroxisome metabolism and biogenesis.
Waterham HR, Ferdinandusse S, Wanders RJ. Waterham HR, et al. Among authors: ferdinandusse s. Biochim Biophys Acta. 2016 May;1863(5):922-33. doi: 10.1016/j.bbamcr.2015.11.015. Epub 2015 Nov 22. Biochim Biophys Acta. 2016. PMID: 26611709 Free article. Review.
Peroxisomes, lipid metabolism and lipotoxicity.
Wanders RJ, Ferdinandusse S, Brites P, Kemp S. Wanders RJ, et al. Among authors: ferdinandusse s. Biochim Biophys Acta. 2010 Mar;1801(3):272-80. doi: 10.1016/j.bbalip.2010.01.001. Epub 2010 Jan 12. Biochim Biophys Acta. 2010. PMID: 20064629 Review.
Phosphomevalonate kinase deficiency expands the genetic spectrum of systemic autoinflammatory diseases.
Berner J, van de Wetering C, Jimenez Heredia R, Rashkova C, Ferdinandusse S, Koster J, Weiss JG, Frohne A, Giuliani S, Waterham HR, Castanon I, Brunner J, Boztug K. Berner J, et al. Among authors: ferdinandusse s. J Allergy Clin Immunol. 2023 Oct;152(4):1025-1031.e2. doi: 10.1016/j.jaci.2023.06.013. Epub 2023 Jun 25. J Allergy Clin Immunol. 2023. PMID: 37364720 Free PMC article.
Zellweger spectrum disorders: clinical overview and management approach.
Klouwer FC, Berendse K, Ferdinandusse S, Wanders RJ, Engelen M, Poll-The BT. Klouwer FC, et al. Among authors: ferdinandusse s. Orphanet J Rare Dis. 2015 Dec 1;10:151. doi: 10.1186/s13023-015-0368-9. Orphanet J Rare Dis. 2015. PMID: 26627182 Free PMC article. Review.
180 results