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Case report: Thirty-year progression of an EMPF1 encephalopathy due to defective mitochondrial and peroxisomal fission caused by a novel de novo heterozygous DNM1L variant.
Lhuissier C, Wagner BE, Vincent A, Garraux G, Hougrand O, Van Coster R, Benoit V, Karadurmus D, Lenaers G, Gueguen N, Chevrollier A, Maystadt I. Lhuissier C, et al. Among authors: garraux g. Front Neurol. 2022 Sep 23;13:937885. doi: 10.3389/fneur.2022.937885. eCollection 2022. Front Neurol. 2022. PMID: 36212643 Free PMC article.
Neural and cognitive bases of upper limb apraxia in corticobasal degeneration.
Peigneux P, Salmon E, Garraux G, Laureys S, Willems S, Dujardin K, Degueldre C, Lemaire C, Luxen A, Moonen G, Franck G, Destee A, Van der Linden M. Peigneux P, et al. Among authors: garraux g. Neurology. 2001 Oct 9;57(7):1259-68. doi: 10.1212/wnl.57.7.1259. Neurology. 2001. PMID: 11591846
81 results