Transcranial magnetic stimulation studies in complex regional pain syndrome type I: A review.
Nardone, R; Brigo, F; Höller, Y; Sebastianelli, L; Versace, V; Saltuari, L; Lochner, P; Trinka, E;
Acta Neurol Scand. 2018; 137(2):158-164
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Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria.
Höglinger, GU; Respondek, G; Stamelou, M; Kurz, C; Josephs, KA; Lang, AE; Mollenhauer, B; Müller, U; Nilsson, C; Whitwell, JL; Arzberger, T; Englund, E; Gelpi, E; Giese, A; Irwin, DJ; Meissner, WG; Pantelyat, A; Rajput, A; van Swieten, JC; Troakes, C; Antonini, A; Bhatia, KP; Bordelon, Y; Compta, Y; Corvol, JC; Colosimo, C; Dickson, DW; Dodel, R; Ferguson, L; Grossman, M; Kassubek, J; Krismer, F; Levin, J; Lorenzl, S; Morris, HR; Nestor, P; Oertel, WH; Poewe, W; Rabinovici, G; Rowe, JB; Schellenberg, GD; Seppi, K; van Eimeren, T; Wenning, GK; Boxer, AL; Golbe, LI; Litvan, I;
Mov Disord. 2017; 32(6): 853-864.
Full papers/articles (Journal)

Which ante mortem clinical features predict progressive supranuclear palsy pathology?
Respondek, G; Kurz, C; Arzberger, T; Compta, Y; Englund, E; Ferguson, LW; Gelpi, E; Giese, A; Irwin, DJ; Meissner, WG; Nilsson, C; Pantelyat, A; Rajput, A; van Swieten, JC; Troakes, C; Josephs, KA; Lang, AE; Mollenhauer, B; Müller, U; Whitwell, JL; Antonini, A; Bhatia, KP; Bordelon, Y; Corvol, JC; Colosimo, C; Dodel, R; Grossman, M; Kassubek, J; Krismer, F; Levin, J; Lorenzl, S; Morris, H; Nestor, P; Oertel, WH; Rabinovici, GD; Rowe, JB; van Eimeren, T; Wenning, GK; Boxer, A; Golbe, LI; Litvan, I; Stamelou, M; Höglinger, GU;
Mov Disord. 2017; 32(7): 995-1005.
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The association of aphasia and right-sided motor impairment in corticobasal syndrome.
Levin, J; Bak, TH; Rominger, A; Mille, E; Arzberger, T; Giese, A; Ackl, N; Lorenzl, S; Bader, B; Patzig, M; Bötzel, K; Danek, A;
J Neurol. 2015; 262(10): 2241-2246.
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Esophageal motility and 24-h pH profiles of patients with heterotopic gastric mucosa in the cervical esophagus.
Korkut, E; Bektaş, M; Alkan, M; Ustün, Y; Meco, C; Ozden, A; Soykan, I;
Eur J Intern Med. 2010; 21(1): 21-24.
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Phenotype variability in spinocerebellar ataxia type 2: a longitudinal family survey and a case featuring an unusual benign course of disease.
Hering, S; Achmüller, C; Köhler, A; Poewe, W; Schneider, R; Boesch, SM;
Mov Disord. 2009; 24(5): 774-777.
Notes

[Behavior therapy in gastrointestinal functional disorders].
Cuntz, U; Pollmann, H; Enck, P;
Z Gastroenterol. 1992; 30(1): 24-34.
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