Klein C - Search Results

1

The Rostock International Parkinson's Disease (ROPAD) Study: Protocol and Initial Findings.

Skrahina V, Gaber H, Vollstedt EJ, Förster TM, Usnich T, Curado F, Brüggemann N, Paul J, Bogdanovic X, Zülbahar S, Olmedillas M, Skobalj S, Ameziane N, Bauer P, Csoti I, Koleva-Alazeh N, Grittner U, Westenberger A, Kasten M, Beetz C, Klein C, Rolfs A; ROPAD Study Group. Skrahina V, et al. Among authors: klein c. Mov Disord. 2021 Apr;36(4):1005-1010. doi: 10.1002/mds.28416. Epub 2020 Dec 14. Mov Disord. 2021. PMID: 33314351 Free PMC article.

2

Fahr's disease--far from a disease.

Klein C, Vieregge P. Klein C, et al. Mov Disord. 1998 May;13(3):620-1. doi: 10.1002/mds.870130350. Mov Disord. 1998. PMID: 9613773 No abstract available.

3

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

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

Data protection in biomaterial banks for Parkinson's disease research: the model of GEPARD (Gene Bank Parkinson's Disease Germany).

Eggert K, Wüllner U, Antony G, Gasser T, Janetzky B, Klein C, Schöls L, Oertel W. Eggert K, et al. Among authors: klein c. Mov Disord. 2007 Apr 15;22(5):611-8. doi: 10.1002/mds.21331. Mov Disord. 2007. PMID: 17230444

8

Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation-dependent probe amplification.

Djarmati A, Guzvić M, Grünewald A, Lang AE, Pramstaller PP, Simon DK, Kaindl AM, Vieregge P, Nygren AO, Beetz C, Hedrich K, Klein C. Djarmati A, et al. Among authors: klein c. Mov Disord. 2007 Sep 15;22(12):1708-14. doi: 10.1002/mds.21370. Mov Disord. 2007. PMID: 17674414

9

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

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

4,052 results

Search Page

Filters