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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. Among authors: glocker fx. Front Immunol. 2019 Mar 21;10:412. doi: 10.3389/fimmu.2019.00412. eCollection 2019. Front Immunol. 2019. PMID: 30949164 Free PMC article.
[Causes of camptocormia].
Glocker FX, Berninger UG. Glocker FX, et al. Nervenarzt. 2013 Aug;84(8):1007-15; quiz 1016. doi: 10.1007/s00115-013-3827-3. Nervenarzt. 2013. PMID: 23903496 German.
[The new S2k AWMF guideline for the treatment of Bell's palsy in commented short form].
Heckmann JG, Lang C, Glocker FX, Urban P, Bischoff C, Weder B, Reiter G, Meier U, Guntinas-Lichius O; Association of the Scientific Medical Societies in Germany (AWMF). Heckmann JG, et al. Among authors: glocker fx. Laryngorhinootologie. 2012 Nov;91(11):686-92. doi: 10.1055/s-0032-1323685. Epub 2012 Sep 7. Laryngorhinootologie. 2012. PMID: 22961063 Review. German.
36 months observational clinical study of 38 adult Pompe disease patients under alglucosidase alfa enzyme replacement therapy.
Regnery C, Kornblum C, Hanisch F, Vielhaber S, Strigl-Pill N, Grunert B, Müller-Felber W, Glocker FX, Spranger M, Deschauer M, Mengel E, Schoser B. Regnery C, et al. Among authors: glocker fx. J Inherit Metab Dis. 2012 Sep;35(5):837-45. doi: 10.1007/s10545-012-9451-8. Epub 2012 Jan 31. J Inherit Metab Dis. 2012. PMID: 22290025 Clinical Trial.
57 results