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

Year Number of Results
2002 1
2003 3
2004 2
2005 5
2006 5
2007 2
2008 3
2009 2
2010 5
2011 5
2012 7
2013 2
2014 5
2015 3
2016 4
2017 3
2018 2
2019 9
2020 9
2021 11
2022 8
2023 5
2024 2

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92 results

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Page 1
X-linked adrenoleukodystrophy: pathogenesis and treatment.
Engelen M, Kemp S, Poll-The BT. Engelen M, et al. Among authors: kemp s. Curr Neurol Neurosci Rep. 2014 Oct;14(10):486. doi: 10.1007/s11910-014-0486-0. Curr Neurol Neurosci Rep. 2014. PMID: 25115486 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: kemp 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.
ABCD1 Transporter Deficiency Results in Altered Cholesterol Homeostasis.
Buda A, Forss-Petter S, Hua R, Jaspers Y, Lassnig M, Waidhofer-Söllner P, Kemp S, Kim P, Weinhofer I, Berger J. Buda A, et al. Among authors: kemp s. Biomolecules. 2023 Aug 31;13(9):1333. doi: 10.3390/biom13091333. Biomolecules. 2023. PMID: 37759733 Free PMC article.
Endocrine dysfunction in adrenoleukodystrophy.
Engelen M, Kemp S, Eichler F. Engelen M, et al. Among authors: kemp s. Handb Clin Neurol. 2021;182:257-267. doi: 10.1016/B978-0-12-819973-2.00018-6. Handb Clin Neurol. 2021. PMID: 34266597 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: kemp 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.
Evolution of adrenoleukodystrophy model systems.
Montoro R, Heine VM, Kemp S, Engelen M. Montoro R, et al. Among authors: kemp s. J Inherit Metab Dis. 2021 May;44(3):544-553. doi: 10.1002/jimd.12357. Epub 2021 Jan 7. J Inherit Metab Dis. 2021. PMID: 33373044 Free PMC article. Review.
Molecular Biomarkers for Adrenoleukodystrophy: An Unmet Need.
Honey MIJ, Jaspers YRJ, Engelen M, Kemp S, Huffnagel IC. Honey MIJ, et al. Among authors: kemp s. Cells. 2021 Dec 6;10(12):3427. doi: 10.3390/cells10123427. Cells. 2021. PMID: 34943935 Free PMC article. Review.
92 results