Klein C - Search Results

1

Co-occurrence of affective and schizophrenia spectrum disorders with PINK1 mutations.

Steinlechner S, Stahlberg J, Völkel B, Djarmati A, Hagenah J, Hiller A, Hedrich K, König I, Klein C, Lencer R. Steinlechner S, et al. Among authors: klein c. J Neurol Neurosurg Psychiatry. 2007 May;78(5):532-5. doi: 10.1136/jnnp.2006.105676. Epub 2007 Jan 3. J Neurol Neurosurg Psychiatry. 2007. PMID: 17202228 Free PMC article.

2

Exclusion of chromosome regions 6p12 and 15q11, but not chromosome region 7p11, in a German family with autosomal dominant congenital nystagmus.

Klein C, Vieregge P, Heide W, Kemper B, Hagedorn-Greiwe M, Hagenah J, Vollmer C, Breakefield XO, Kömpf D, Ozelius L. Klein C, et al. Genomics. 1998 Nov 15;54(1):176-7. doi: 10.1006/geno.1998.5535. Genomics. 1998. PMID: 9806847 No abstract available.

3

Exogenous levodopa is not toxic to elderly subjects with non-parkinsonian movement disorders: further clinical evidence.

Hagenah J, Klein C, Sieberer M, Vieregge P. Hagenah J, et al. Among authors: klein c. J Neural Transm (Vienna). 1999;106(3-4):301-7. doi: 10.1007/s007020050159. J Neural Transm (Vienna). 1999. PMID: 10392538

4

Parkinson's disease in twins: a follow-up study.

Vieregge P, Hagenah J, Heberlein I, Klein C, Ludin HP. Vieregge P, et al. Among authors: klein c. Neurology. 1999 Aug 11;53(3):566-72. doi: 10.1212/wnl.53.3.566. Neurology. 1999. PMID: 10449122

5

Neuropsychological abnormalities in first degree relatives of patients with familial Parkinson's disease.

Kis B, Heberlein I, Hagenah J, Jacobs H, Klein C, Vieregge P. Kis B, et al. Among authors: klein c. J Neurol Neurosurg Psychiatry. 2000 Dec;69(6):838. doi: 10.1136/jnnp.69.6.838. J Neurol Neurosurg Psychiatry. 2000. PMID: 11185648 Free PMC article. No abstract available.

6

Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin gene.

Hilker R, Klein C, Ghaemi M, Kis B, Strotmann T, Ozelius LJ, Lenz O, Vieregge P, Herholz K, Heiss WD, Pramstaller PP. Hilker R, et al. Among authors: klein c. Ann Neurol. 2001 Mar;49(3):367-76. Ann Neurol. 2001. PMID: 11261512

7

Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia.

Zühlke C, Hellenbroich Y, Dalski A, Kononowa N, Hagenah J, Vieregge P, Riess O, Klein C, Schwinger E. Zühlke C, et al. Among authors: klein c. Eur J Hum Genet. 2001 Mar;9(3):160-4. doi: 10.1038/sj.ejhg.5200617. Eur J Hum Genet. 2001. PMID: 11313753

8

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

9

Parkin mutations in a patient with hemiparkinsonism-hemiatrophy: a clinical-genetic and PET study.

Pramstaller PP, Künig G, Leenders K, Kann M, Hedrich K, Vieregge P, Goetz CG, Klein C. Pramstaller PP, et al. Among authors: klein c. Neurology. 2002 Mar 12;58(5):808-10. doi: 10.1212/wnl.58.5.808. Neurology. 2002. PMID: 11889248

10

Evaluation of 50 probands with early-onset Parkinson's disease for Parkin mutations.

Hedrich K, Marder K, Harris J, Kann M, Lynch T, Meija-Santana H, Pramstaller PP, Schwinger E, Bressman SB, Fahn S, Klein C. Hedrich K, et al. Among authors: klein c. Neurology. 2002 Apr 23;58(8):1239-46. doi: 10.1212/wnl.58.8.1239. Neurology. 2002. PMID: 11971093

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