Kessler KR - Search Results

1

Dopaminergic function in a family with the PARK6 form of autosomal recessive Parkinson's syndrome.

Kessler KR, Hamscho N, Morales B, Menzel C, Barrero F, Vives F, Gispert S, Auburger G. Kessler KR, et al. J Neural Transm (Vienna). 2005 Oct;112(10):1345-53. doi: 10.1007/s00702-005-0281-9. Epub 2005 Mar 23. J Neural Transm (Vienna). 2005. PMID: 15785866

2

Sleep quality in a family with hereditary parkinsonism (PARK6).

Tuin I, Voss U, Kessler K, Krakow K, Hilker R, Morales B, Steinmetz H, Auburger G. Tuin I, et al. Sleep Med. 2008 Aug;9(6):684-8. doi: 10.1016/j.sleep.2007.07.004. Epub 2007 Sep 4. Sleep Med. 2008. PMID: 17766179

3

Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant inheritance and purely focal distribution.

Leube B, Rudnicki D, Ratzlaff T, Kessler KR, Benecke R, Auburger G. Leube B, et al. Among authors: kessler kr. Hum Mol Genet. 1996 Oct;5(10):1673-7. doi: 10.1093/hmg/5.10.1673. Hum Mol Genet. 1996. PMID: 8894706

4

Sporadic focal dystonia in northwest Germany: molecular basis on chromosome 18p.

Leube B, Hendgen T, Kessler KR, Knapp M, Benecke R, Auburger G. Leube B, et al. Among authors: kessler kr. Ann Neurol. 1997 Jul;42(1):111-4. doi: 10.1002/ana.410420117. Ann Neurol. 1997. PMID: 9225692

5

Evidence for DYT7 being a common cause of cervical dystonia (torticollis) in Central Europe.

Leube B, Hendgen T, Kessler KR, Knapp M, Benecke R, Auburger G. Leube B, et al. Among authors: kessler kr. Am J Med Genet. 1997 Sep 19;74(5):529-32. doi: 10.1002/(sici)1096-8628(19970919)74:5<529::aid-ajmg15>3.0.co;2-e. Am J Med Genet. 1997. PMID: 9342206

6

Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family.

Leube B, Kessler KR, Goecke T, Auburger G, Benecke R. Leube B, et al. Among authors: kessler kr. Mov Disord. 1997 Nov;12(6):1000-6. doi: 10.1002/mds.870120625. Mov Disord. 1997. PMID: 9399227

7

Stages of sleep pathology in spinocerebellar ataxia type 2 (SCA2).

Tuin I, Voss U, Kang JS, Kessler K, Rüb U, Nolte D, Lochmüller H, Tinschert S, Claus D, Krakow K, Pflug B, Steinmetz H, Auburger G. Tuin I, et al. Neurology. 2006 Dec 12;67(11):1966-72. doi: 10.1212/01.wnl.0000247054.90322.14. Neurology. 2006. PMID: 17159102

8

Phenotypic variability of the DYT1 mutation in German dystonia patients.

Leube B, Kessler KR, Ferbert A, Ebke M, Schwendemann G, Erbguth F, Benecke R, Auburger G. Leube B, et al. Among authors: kessler kr. Acta Neurol Scand. 1999 Apr;99(4):248-51. doi: 10.1111/j.1600-0404.1999.tb07356.x. Acta Neurol Scand. 1999. PMID: 10225357

9

Secondary progressive chronic manganism associated with markedly decreased striatal D2 receptor density.

Kessler KR, Wunderlich G, Hefter H, Seitz RJ. Kessler KR, et al. Mov Disord. 2003 Feb;18(2):217-8. doi: 10.1002/mds.10325. Mov Disord. 2003. PMID: 12539219

10

Differences in age at onset and familial aggregation between clinical types of idiopathic Parkinson's disease.

Korchounov A, Schipper HI, Preobrazhenskaya IS, Kessler KR, Yakhno NN. Korchounov A, et al. Among authors: kessler kr. Mov Disord. 2004 Sep;19(9):1059-64. doi: 10.1002/mds.20061. Mov Disord. 2004. PMID: 15372596

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