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A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin.
Abicht A, Stucka R, Karcagi V, Herczegfalvi A, Horváth R, Mortier W, Schara U, Ramaekers V, Jost W, Brunner J, Janssen G, Seidel U, Schlotter B, Müller-Felber W, Pongratz D, Rüdel R, Lochmüller H. Abicht A, et al. Among authors: jost w. Neurology. 1999 Oct 22;53(7):1564-9. doi: 10.1212/wnl.53.7.1564. Neurology. 1999. PMID: 10534268
[Myositis caused by a mycoplasma infection].
Brunner J, Jost W. Brunner J, et al. Among authors: jost w. Klin Padiatr. 2000 May-Jun;212(3):129-30. doi: 10.1055/s-2000-9666. Klin Padiatr. 2000. PMID: 10916786 German.
Nationwide Retrospective Analysis of Combinations of Advanced Therapies in Patients With Parkinson Disease.
Pürner D, Hormozi M, Weiß D, Barbe MT, Jergas H, Prell T, Gülke E, Pötter-Nerger M, Falkenburger B, Klingelhöfer L, Gutsmiedl PK, Haslinger B, Jochim AM, Wolff A, Schröter N, Rijntjes M, van Riesen C, Scheller U, Wolz M, Amouzandeh A, Ebersbach G, Gruber D, Kohl Z, Maetzler W, Paschen S, Pérez-González P, Rozanski V, Schwarz J, Südmeyer M, Torka E, Wesbuer S, Bornmann S, Flöel A, Ip CW, Krause P, Kühn AA, Csoti I, Herting B, van de Loo S, Basheer AA, Liszka R, Jost WH, Koschel J, Haller B, Lingor P. Pürner D, et al. Among authors: jost wh. Neurology. 2023 Nov 21;101(21):e2078-e2093. doi: 10.1212/WNL.0000000000207858. Epub 2023 Nov 1. Neurology. 2023. PMID: 37914414
The phenylalanine loading test in the differential diagnosis of dystonia.
Bandmann O, Goertz M, Zschocke J, Deuschl G, Jost W, Hefter H, Müller U, Zöfel P, Hoffmann G, Oertel W. Bandmann O, et al. Among authors: jost w. Neurology. 2003 Feb 25;60(4):700-2. doi: 10.1212/01.wnl.0000048205.18445.98. Neurology. 2003. PMID: 12601115 Clinical Trial.
371 results