Klein C - Search Results

1

Launching the movement disorders society genetic mutation database (MDSGene).

Lill CM, Mashychev A, Hartmann C, Lohmann K, Marras C, Lang AE, Klein C, Bertram L. Lill CM, et al. Among authors: klein c. Mov Disord. 2016 May;31(5):607-9. doi: 10.1002/mds.26651. Mov Disord. 2016. PMID: 27156390 Review. No abstract available.

2

Voluntary palatal tremor in two siblings.

Klein C, Gehrking E, Vieregge P. Klein C, et al. Mov Disord. 1998 May;13(3):545-8. doi: 10.1002/mds.870130328. Mov Disord. 1998. PMID: 9613751

3

Concordant late onset of craniocervical dystonia in a pair of monozygotic twins.

Sieberer MG, Vieregge P, Klein C, Ozelius LJ, Wandinger KP. Sieberer MG, et al. Among authors: klein c. Mov Disord. 1999 Nov;14(6):1040-3. doi: 10.1002/1531-8257(199911)14:6<1040::aid-mds1025>3.0.co;2-9. Mov Disord. 1999. PMID: 10584687 No abstract available.

4

A major locus for myoclonus-dystonia maps to chromosome 7q in eight families.

Klein C, Schilling K, Saunders-Pullman RJ, Garrels J, Breakefield XO, Brin MF, deLeon D, Doheny D, Fahn S, Fink JS, Forsgren L, Friedman J, Frucht S, Harris J, Holmgren G, Kis B, Kurlan R, Kyllerman M, Lang AE, Leung J, Raymond D, Robishaw JD, Sanner G, Schwinger E, Tabamo RE, Tagliati M. Klein C, et al. Am J Hum Genet. 2000 Nov;67(5):1314-9. Epub 2000 Oct 5. Am J Hum Genet. 2000. PMID: 11022010 Free PMC article.

5

The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism.

Hedrich K, Kann M, Lanthaler AJ, Dalski A, Eskelson C, Landt O, Schwinger E, Vieregge P, Lang AE, Breakefield XO, Ozelius LJ, Pramstaller PP, Klein C. Hedrich K, et al. Among authors: klein c. Hum Mol Genet. 2001 Aug 1;10(16):1649-56. doi: 10.1093/hmg/10.16.1649. Hum Mol Genet. 2001. PMID: 11487568

6

DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease.

Hedrich K, Djarmati A, Schäfer N, Hering R, Wellenbrock C, Weiss PH, Hilker R, Vieregge P, Ozelius LJ, Heutink P, Bonifati V, Schwinger E, Lang AE, Noth J, Bressman SB, Pramstaller PP, Riess O, Klein C. Hedrich K, et al. Among authors: klein c. Neurology. 2004 Feb 10;62(3):389-94. doi: 10.1212/01.wnl.0000113022.51739.88. Neurology. 2004. PMID: 14872018

7

Co-occurrence of restless legs syndrome and Parkin mutations in two families.

Adel S, Djarmati A, Kabakci K, Pichler I, Eskelson C, Lohnau T, Kock N, Hagenah J, Hedrich K, Schwinger E, Kramer PL, Pramstaller PP, Klein C. Adel S, et al. Among authors: klein c. Mov Disord. 2006 Feb;21(2):258-63. doi: 10.1002/mds.20690. Mov Disord. 2006. PMID: 16161156

8

The 'essentials' of essential palatal tremor: a reappraisal of the nosology.

Zadikoff C, Lang AE, Klein C. Zadikoff C, et al. Among authors: klein c. Brain. 2006 Apr;129(Pt 4):832-40. doi: 10.1093/brain/awh684. Epub 2005 Nov 29. Brain. 2006. PMID: 16317025 Review.

9

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

10

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

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