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Nonmotor symptoms in genetic Parkinson disease.
Kasten M, Kertelge L, Brüggemann N, van der Vegt J, Schmidt A, Tadic V, Buhmann C, Steinlechner S, Behrens MI, Ramirez A, Binkofski F, Siebner H, Raspe H, Hagenah J, Lencer R, Klein C. Kasten M, et al. Among authors: schmidt a. Arch Neurol. 2010 Jun;67(6):670-6. doi: 10.1001/archneurol.67.6.670. Arch Neurol. 2010. PMID: 20558386 Review.
The role of genes in causing dystonia.
Schmidt A, Klein C. Schmidt A, et al. Eur J Neurol. 2010 Jul;17 Suppl 1:65-70. doi: 10.1111/j.1468-1331.2010.03055.x. Eur J Neurol. 2010. PMID: 20590811 Review.
Impaired sense of smell and color discrimination in monogenic and idiopathic Parkinson's disease.
Kertelge L, Brüggemann N, Schmidt A, Tadic V, Wisse C, Dankert S, Drude L, van der Vegt J, Siebner H, Pawlack H, Pramstaller PP, Behrens MI, Ramirez A, Reichel D, Buhmann C, Hagenah J, Klein C, Lohmann K, Kasten M. Kertelge L, et al. Among authors: schmidt a. Mov Disord. 2010 Nov 15;25(15):2665-9. doi: 10.1002/mds.23272. Mov Disord. 2010. PMID: 20721915
Clinical spectrum of Kufor-Rakeb syndrome in the Chilean kindred with ATP13A2 mutations.
Behrens MI, Brüggemann N, Chana P, Venegas P, Kägi M, Parrao T, Orellana P, Garrido C, Rojas CV, Hauke J, Hahnen E, González R, Seleme N, Fernández V, Schmidt A, Binkofski F, Kömpf D, Kubisch C, Hagenah J, Klein C, Ramirez A. Behrens MI, et al. Among authors: schmidt a. Mov Disord. 2010 Sep 15;25(12):1929-37. doi: 10.1002/mds.22996. Mov Disord. 2010. PMID: 20683840
Exome sequencing in a family with restless legs syndrome.
Weissbach A, Siegesmund K, Brüggemann N, Schmidt A, Kasten M, Pichler I, Muhle H, Lohmann E, Lohnau T, Schwinger E, Hagenah J, Stephani U, Pramstaller PP, Klein C, Lohmann K. Weissbach A, et al. Among authors: schmidt a. Mov Disord. 2012 Nov;27(13):1686-9. doi: 10.1002/mds.25191. Mov Disord. 2012. PMID: 23192925
6,634 results