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New Variant of MELAS Syndrome With Executive Dysfunction, Heteroplasmic Point Mutation in the MT-ND4 Gene (m.12015T>C; p.Leu419Pro) and Comorbid Polyglandular Autoimmune Syndrome Type 2.
Endres D, Süß P, Maier SJ, Friedel E, Nickel K, Ziegler C, Fiebich BL, Glocker FX, Stock F, Egger K, Lange T, Dacko M, Venhoff N, Erny D, Doostkam S, Komlosi K, Domschke K, Tebartz van Elst L. Endres D, et al. Front Immunol. 2019 Mar 21;10:412. doi: 10.3389/fimmu.2019.00412. eCollection 2019. Front Immunol. 2019. PMID: 30949164 Free PMC article.
Retinal Thinning in Adults with Autism Spectrum Disorder.
Friedel EBN, Tebartz van Elst L, Schäfer M, Maier S, Runge K, Küchlin S, Reich M, Lagrèze WA, Kornmeier J, Ebert D, Endres D, Domschke K, Nickel K. Friedel EBN, et al. J Autism Dev Disord. 2024 Mar;54(3):1143-1156. doi: 10.1007/s10803-022-05882-8. Epub 2022 Dec 23. J Autism Dev Disord. 2024. PMID: 36550331 Free PMC article.
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