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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
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Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 (Genome Medicine, (2023), 15, 1, (22), 10.1186/s13073-023-01173-8)
COVIDeF Study Group, French COVID Cohort Study Group, CoV-Contact Cohort, COVID-STORM Clinicians, COVID Clinicians, Orchestra Working Group, Amsterdam UMC Covid-19 Biobank, NIAID-USUHS COVID Study Group & COVID Human Genetic Effort, Dec 2024, In: Genome Medicine. 16, 1, 6.Research output: Contribution to journal › Comment/Letter to the editor › Academic
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Proteomic dissection of vanishing white matter pathogenesis
Man, J. H. K., Zarekiani, P., Mosen, P., de Kok, M., Debets, D. O., Breur, M., Altelaar, M., van der Knaap, M. S. & Bugiani, M., Dec 2024, In: Cellular and molecular life sciences : CMLS. 81, 1, p. 234 1 p., 234.Research output: Contribution to journal › Article › Academic › peer-review
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