Klein C - Search Results

1

Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotype.

Klein C, Pramstaller PP, Kis B, Page CC, Kann M, Leung J, Woodward H, Castellan CC, Scherer M, Vieregge P, Breakefield XO, Kramer PL, Ozelius LJ. Klein C, et al. Ann Neurol. 2000 Jul;48(1):65-71. Ann Neurol. 2000. PMID: 10894217

2

Paroxysmal choreoathetosis in a patient with idiopathic basal ganglia calcification, chorea, and dystonia.

Klein C, Vieregge P, Kömpf D. Klein C, et al. Mov Disord. 1997 Mar;12(2):254-5. doi: 10.1002/mds.870120223. Mov Disord. 1997. PMID: 9087991 No abstract available.

3

Gait quantitation in Parkinson's disease--locomotor disability and correlation to clinical rating scales.

Vieregge P, Stolze H, Klein C, Heberlein I. Vieregge P, et al. Among authors: klein c. J Neural Transm (Vienna). 1997;104(2-3):237-48. doi: 10.1007/BF01273184. J Neural Transm (Vienna). 1997. PMID: 9203085 Clinical Trial.

4

The diagnosis of 'essential palatal tremor'.

Vieregge P, Klein C, Gehrking E, Körtke D, Kömpf D. Vieregge P, et al. Among authors: klein c. Neurology. 1997 Jul;49(1):248-9. doi: 10.1212/wnl.49.1.248. Neurology. 1997. PMID: 9222198

5

A study of visual hallucinations in patients with Parkinson's disease.

Klein C, Kömpf D, Pulkowski U, Moser A, Vieregge P. Klein C, et al. J Neurol. 1997 Jun;244(6):371-7. doi: 10.1007/s004150050104. J Neurol. 1997. PMID: 9249622 Clinical Trial.

6

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

7

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.

8

De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia.

Klein C, Brin MF, de Leon D, Limborska SA, Ivanova-Smolenskaya IA, Bressman SB, Friedman A, Markova ED, Risch NJ, Breakefield XO, Ozelius LJ. Klein C, et al. Hum Mol Genet. 1998 Jul;7(7):1133-6. doi: 10.1093/hmg/7.7.1133. Hum Mol Genet. 1998. PMID: 9618171

9

Clinical and genetic evaluation of a family with a mixed dystonia phenotype from South Tyrol.

Klein C, Pramstaller PP, Castellan CC, Breakefield XO, Kramer PL, Ozelius LJ. Klein C, et al. Ann Neurol. 1998 Sep;44(3):394-8. doi: 10.1002/ana.410440318. Ann Neurol. 1998. PMID: 9749609

10

[Non-epileptic paroxysmal movement disorders].

Klein C, Vieregge P. Klein C, et al. Nervenarzt. 1998 Aug;69(8):647-59. doi: 10.1007/s001150050324. Nervenarzt. 1998. PMID: 9757415 Review. German.

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