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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 8
2024 6
2025 2

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185 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 fatty acid homeostasis.
Vaz FM, Ferdinandusse S, Salomons GS, Wanders RJA. Vaz FM, et al. Among authors: ferdinandusse s. J Inherit Metab Dis. 2024 May 1. doi: 10.1002/jimd.12734. Online ahead of print. J Inherit Metab Dis. 2024. PMID: 38693715 Review.
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.
Discovery of novel diagnostic biomarkers for Sjögren-Larsson syndrome by untargeted lipidomics.
Vaz FM, Staps P, van Klinken JB, van Lenthe H, Vervaart M, Wanders RJA, Pras-Raves ML, van Weeghel M, Salomons GS, Ferdinandusse S, Wevers RA, Willemsen MAAP. Vaz FM, et al. Among authors: ferdinandusse s. Biochim Biophys Acta Mol Cell Biol Lipids. 2024 Mar;1869(2):159447. doi: 10.1016/j.bbalip.2023.159447. Epub 2024 Jan 3. Biochim Biophys Acta Mol Cell Biol Lipids. 2024. PMID: 38181883 Free article.
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.
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.
Vision on gyrate atrophy: why treat the eye?
Bergen AA, Buijs MJ, Ten Asbroek AL, Balfoort BM, Boon CJ; Dutch GACR “Bird’s Eye View” Consortium; Brands MM, Wanders RJ, van Karnebeek CD, Houtkooper RH. Bergen AA, et al. EMBO Mol Med. 2024 Jan;16(1):4-7. doi: 10.1038/s44321-023-00001-1. Epub 2023 Dec 14. EMBO Mol Med. 2024. PMID: 38177529 Free PMC article.
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.
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.
185 results