Klein C - Search Results

1

Clinical and demographic characteristics of PINK1 mutation carriers--a meta-analysis.

Kasten M, Weichert C, Lohmann K, Klein C. Kasten M, et al. Among authors: klein c. Mov Disord. 2010 May 15;25(7):952-4. doi: 10.1002/mds.23031. Mov Disord. 2010. PMID: 20461815 No abstract available.

2

Motor reorganization in asymptomatic carriers of a single mutant Parkin allele: a human model for presymptomatic parkinsonism.

Buhmann C, Binkofski F, Klein C, Büchel C, van Eimeren T, Erdmann C, Hedrich K, Kasten M, Hagenah J, Deuschl G, Pramstaller PP, Siebner HR. Buhmann C, et al. Among authors: klein c. Brain. 2005 Oct;128(Pt 10):2281-90. doi: 10.1093/brain/awh572. Epub 2005 Jun 9. Brain. 2005. PMID: 15947065

3

Homozygous and heterozygous PINK1 mutations: considerations for diagnosis and care of Parkinson's disease patients.

Zadikoff C, Rogaeva E, Djarmati A, Sato C, Salehi-Rad S, St George-Hyslop P, Klein C, Lang AE. Zadikoff C, et al. Among authors: klein c. Mov Disord. 2006 Jun;21(6):875-9. doi: 10.1002/mds.20854. Mov Disord. 2006. PMID: 16547921

4

Heterozygous PINK1 mutations: a susceptibility factor for Parkinson disease?

Djarmati A, Hedrich K, Svetel M, Lohnau T, Schwinger E, Romac S, Pramstaller PP, Kostić V, Klein C. Djarmati A, et al. Among authors: klein c. Mov Disord. 2006 Sep;21(9):1526-30. doi: 10.1002/mds.20977. Mov Disord. 2006. PMID: 16755580

5

Recurrent LRRK2 (Park8) mutations in early-onset Parkinson's disease.

Hedrich K, Winkler S, Hagenah J, Kabakci K, Kasten M, Schwinger E, Volkmann J, Pramstaller PP, Kostic V, Vieregge P, Klein C. Hedrich K, et al. Among authors: klein c. Mov Disord. 2006 Sep;21(9):1506-10. doi: 10.1002/mds.20990. Mov Disord. 2006. PMID: 16758483

6

Phenotypic spectrum of PINK1-associated parkinsonism in 15 mutation carriers from 1 family.

Hiller A, Hagenah JM, Djarmati A, Hedrich K, Reetz K, Schneider-Gold C, Kress W, Münchau A, Klein C. Hiller A, et al. Among authors: klein c. Mov Disord. 2007 Jan;22(1):145-7. doi: 10.1002/mds.21059. Mov Disord. 2007. PMID: 17013904

7

Substantia nigra hyperechogenicity correlates with clinical status and number of Parkin mutated alleles.

Hagenah JM, König IR, Becker B, Hilker R, Kasten M, Hedrich K, Pramstaller PP, Klein C, Seidel G. Hagenah JM, et al. Among authors: klein c. J Neurol. 2007 Oct;254(10):1407-13. doi: 10.1007/s00415-007-0567-y. Epub 2007 Oct 15. J Neurol. 2007. PMID: 17934880

8

Bilateral subthalamic stimulation in Parkin and PINK1 parkinsonism.

Moro E, Volkmann J, König IR, Winkler S, Hiller A, Hassin-Baer S, Herzog J, Schnitzler A, Lohmann K, Pinsker MO, Voges J, Djarmatic A, Seibler P, Lozano AM, Rogaeva E, Lang AE, Deuschl G, Klein C. Moro E, et al. Among authors: klein c. Neurology. 2008 Apr 1;70(14):1186-91. doi: 10.1212/01.wnl.0000307748.11216.03. Neurology. 2008. PMID: 18378882

9

A heterozygous frameshift mutation in PRKRA (DYT16) associated with generalised dystonia in a German patient.

Seibler P, Djarmati A, Langpap B, Hagenah J, Schmidt A, Brüggemann N, Siebner H, Jabusch HC, Altenmüller E, Münchau A, Lohmann K, Klein C. Seibler P, et al. Among authors: klein c. Lancet Neurol. 2008 May;7(5):380-1. doi: 10.1016/S1474-4422(08)70075-9. Lancet Neurol. 2008. PMID: 18420150 No abstract available.

10

Transcranial sonography findings in a large family with homozygous and heterozygous PINK1 mutations.

Hagenah JM, Becker B, Brüggemann N, Djarmati A, Lohmann K, Sprenger A, Klein C, Seidel G. Hagenah JM, et al. Among authors: klein c. J Neurol Neurosurg Psychiatry. 2008 Sep;79(9):1071-4. doi: 10.1136/jnnp.2007.142174. Epub 2008 May 9. J Neurol Neurosurg Psychiatry. 2008. PMID: 18469032

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