Kis B - Search Results

1

Association studies of Parkinson's disease and parkin polymorphisms.

Klein C, Schumacher K, Jacobs H, Hagenah J, Kis B, Garrels J, Schwinger E, Ozelius L, Pramstaller P, Vieregge P, Kramer PL. Klein C, et al. Among authors: kis b. Ann Neurol. 2000 Jul;48(1):126-7. Ann Neurol. 2000. PMID: 10894229 No abstract available.

2

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. Among authors: kis b. Ann Neurol. 2000 Jul;48(1):65-71. Ann Neurol. 2000. PMID: 10894217

3

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. 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.

4

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: kis b. Ann Neurol. 2001 Mar;49(3):367-76. Ann Neurol. 2001. PMID: 11261512

5

Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene.

Pramstaller PP, Kis B, Eskelson C, Hedrich K, Scherer M, Schwinger E, Breakefield XO, Kramer PL, Ozelius LJ, Klein C. Pramstaller PP, et al. Among authors: kis b. Mov Disord. 2002 Mar;17(2):424-6. doi: 10.1002/mds.10071. Mov Disord. 2002. PMID: 11921141 No abstract available.

6

Oculogyric dystonic states in early-onset parkinsonism with basal ganglia calcifications.

Kis B, Hedrich K, Kann M, Schwinger E, Kömpf D, Klein C, Pramstaller PP. Kis B, et al. Neurology. 2005 Sep 13;65(5):761. doi: 10.1212/01.wnl.0000180349.84136.e1. Neurology. 2005. PMID: 16157916 No abstract available.

7

[Genetics of dystonia].

Klein C, Kann M, Kis B, Pramstaller PP, Breakefield XO, Ozelius LJ, Vieregge P. Klein C, et al. Among authors: kis b. Nervenarzt. 2000 Jun;71(6):431-41. doi: 10.1007/s001150050604. Nervenarzt. 2000. PMID: 10919137 Review. German.

8

Novel three-stage ascertainment method: prevalence of PD and parkinsonism in South Tyrol, Italy.

Kis B, Schrag A, Ben-Shlomo Y, Klein C, Gasperi A, Spoegler F, Schoenhuber R, Pramstaller PP. Kis B, et al. Neurology. 2002 Jun 25;58(12):1820-5. doi: 10.1212/wnl.58.12.1820. Neurology. 2002. PMID: 12084883

9

Brain potential signs of slowed stimulus processing following cholecystokinin in Parkinson's disease.

Smolnik R, Fischer S, Hagenah J, Kis B, Born J, Vieregge P. Smolnik R, et al. Among authors: kis b. Psychopharmacology (Berl). 2002 Apr;161(1):70-6. doi: 10.1007/s00213-002-1010-9. Epub 2002 Feb 19. Psychopharmacology (Berl). 2002. PMID: 11967633 Clinical Trial.

10

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. Among authors: kis b. Am J Hum Genet. 2000 Nov;67(5):1314-9. Epub 2000 Oct 5. Am J Hum Genet. 2000. PMID: 11022010 Free PMC article.

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