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ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia.
Bouwkamp CG, Afawi Z, Fattal-Valevski A, Krabbendam IE, Rivetti S, Masalha R, Quadri M, Breedveld GJ, Mandel H, Tailakh MA, Beverloo HB, Stevanin G, Brice A, van IJcken WFJ, Vernooij MW, Dolga AM, de Vrij FMS, Bonifati V, Kushner SA. Bouwkamp CG, et al. Among authors: krabbendam ie. Neurol Genet. 2018 Mar 21;4(2):e223. doi: 10.1212/NXG.0000000000000223. eCollection 2018 Apr. Neurol Genet. 2018. PMID: 29577077 Free PMC article.
Plasma hsa-mir-19b is a potential LevoDopa therapy marker.
Chis AR, Moatar AI, Dijmarescu C, Rosca C, Vorovenci RJ, Krabbendam I, Dolga A, Bejinar C, Marian C, Sirbu IO, Simu M. Chis AR, et al. J Cell Mol Med. 2021 Sep;25(18):8715-8724. doi: 10.1111/jcmm.16827. Epub 2021 Jul 30. J Cell Mol Med. 2021. PMID: 34328686 Free PMC article.
Negative modulation of mitochondrial calcium uniporter complex protects neurons against ferroptosis.
Marmolejo-Garza A, Krabbendam IE, Luu MDA, Brouwer F, Trombetta-Lima M, Unal O, O'Connor SJ, Majerníková N, Elzinga CRS, Mammucari C, Schmidt M, Madesh M, Boddeke E, Dolga AM. Marmolejo-Garza A, et al. Among authors: krabbendam ie. Cell Death Dis. 2023 Nov 25;14(11):772. doi: 10.1038/s41419-023-06290-1. Cell Death Dis. 2023. PMID: 38007529 Free PMC article.
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