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Small fibre neuropathy in Fabry disease: a human-derived neuronal in vitro disease model and pilot data.
Brain Commun. 2024 Apr 3;6(2):fcae095. doi: 10.1093/braincomms/fcae095. eCollection 2024.
Brain Commun. 2024.
PMID: 38638148
Free PMC article.
Endothelial Cell Dysfunction and Hypoxia as Potential Mediators of Pain in Fabry Disease: A Human-Murine Translational Approach.
Klug K, Spitzel M, Hans C, Klein A, Schottmann NM, Erbacher C, Üçeyler N.
Klug K, et al. Among authors: schottmann nm.
Int J Mol Sci. 2023 Oct 21;24(20):15422. doi: 10.3390/ijms242015422.
Int J Mol Sci. 2023.
PMID: 37895103
Free PMC article.
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Generation of induced pluripotent stem cell line (UKWNLi008) derived from a patient carrying a c.1678C>G variant in the transient receptor potential cation channel subfamily A member (TRPA1) gene potentially associated with small fiber neuropathy.
Schottmann NM, Klug K, Klopocki E, Üçeyler N.
Schottmann NM, et al.
Stem Cell Res. 2023 Jun;69:103094. doi: 10.1016/j.scr.2023.103094. Epub 2023 Apr 12.
Stem Cell Res. 2023.
PMID: 37079968
Free article.
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