Amsterdam Neuroscience
-
Lovastatin in X-Linked Adrenoleukodystrophy
Engelen, M., Ofman, R., Dijkgraaf, M. G. W., Hijzen, M., van der Wardt, L. A., van Geel, B. M., de Visser, M., Wanders, R. J. A., Poll-The, B. T. & Kemp, S., 2010, In: New England journal of medicine. 362, 3, p. 276-277Research output: Contribution to journal › Comment/Letter to the editor › Academic
-
X-linked adrenoleukodystrophy in women: a cross-sectional cohort study
Engelen, M., Barbier, M., Dijkstra, I. M. E., Schür, R., de Bie, R. M. A., Verhamme, C., Dijkgraaf, M. G. W., Aubourg, P. A., Wanders, R. J. A., van Geel, B. M., de Visser, M., Poll-The, B. T. & Kemp, S., 2014, In: Brain. 137, Part 3, p. 693-706Research output: Contribution to journal › Article › Academic › peer-review
-
X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management: Clinical presentation and guidelines for diagnosis, follow-up and management
Engelen, M., Kemp, S., de Visser, M., van Geel, B. M., Wanders, R. J. A., Aubourg, P. & Poll-The, B. T., 2012, In: Orphanet Journal of Rare Diseases. 7, 1Research output: Contribution to journal › Review article › Academic › peer-review
- All publications
-
The pathology of X-linked adrenoleukodystrophy: tissue specific changes as a clue to pathophysiology
Yska, H. A. F., Engelen, M. & Bugiani, M., 1 Dec 2024, In: Orphanet Journal of Rare Diseases. 19, 1, 138.Research output: Contribution to journal › Review article › Academic › peer-review
-
Reduced MUNC18-1 Levels, Synaptic Proteome Changes, and Altered Network Activity in STXBP1-Related Disorder Patient Neurons
van Berkel, A. A., Lammertse, H. C. A., Öttl, M., Koopmans, F., Misra-Isrie, M., Meijer, M., Dilena, R., van Hasselt, P. M., Engelen, M., van Haelst, M., Smit, A. B., van der Sluis, S., Toonen, R. F. & Verhage, M., Jan 2024, In: Biological Psychiatry Global Open Science. 4, 1, p. 284-298 15 p.Research output: Contribution to journal › Article › Academic › peer-review
-
Systematic study of ophthalmological findings in 10 patients with PEX1-mediated Zellweger spectrum disorder
Karuntu, J. S., Klouwer, F. C. C., Engelen, M. & Boon, C. J. F., 2024, (E-pub ahead of print) In: Ophthalmic Genetics.Research output: Contribution to journal › Article › Academic › peer-review
- All publications