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Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: role of a single hit?
Hedrich K, Hagenah J, Djarmati A, Hiller A, Lohnau T, Lasek K, Grünewald A, Hilker R, Steinlechner S, Boston H, Kock N, Schneider-Gold C, Kress W, Siebner H, Binkofski F, Lencer R, Münchau A, Klein C. Hedrich K, et al. Arch Neurol. 2006 Jun;63(6):833-8. doi: 10.1001/archneur.63.6.833. Arch Neurol. 2006. PMID: 16769864
Muscle pathology in 57 patients with myotonic dystrophy type 2.
Schoser BG, Schneider-Gold C, Kress W, Goebel HH, Reilich P, Koch MC, Pongratz DE, Toyka KV, Lochmüller H, Ricker K. Schoser BG, et al. Muscle Nerve. 2004 Feb;29(2):275-81. doi: 10.1002/mus.10545. Muscle Nerve. 2004. PMID: 14755494
Sudden cardiac death in myotonic dystrophy type 2.
Schoser BG, Ricker K, Schneider-Gold C, Hengstenberg C, Dürre J, Bültmann B, Kress W, Day JW, Ranum LP. Schoser BG, et al. Neurology. 2004 Dec 28;63(12):2402-4. doi: 10.1212/01.wnl.0000147335.10783.e4. Neurology. 2004. PMID: 15623712 Review.
Outcome and effect of pregnancy in myotonic dystrophy type 2.
Rudnik-Schöneborn S, Schneider-Gold C, Raabe U, Kress W, Zerres K, Schoser BG. Rudnik-Schöneborn S, et al. Neurology. 2006 Feb 28;66(4):579-80. doi: 10.1212/01.wnl.0000198227.91131.1e. Neurology. 2006. PMID: 16505316
82 results