Gasser T - Search Results

1

Novel mutation in the TOR1A (DYT1) gene in atypical early onset dystonia and polymorphisms in dystonia and early onset parkinsonism.

Leung JC, Klein C, Friedman J, Vieregge P, Jacobs H, Doheny D, Kamm C, DeLeon D, Pramstaller PP, Penney JB, Eisengart M, Jankovic J, Gasser T, Bressman SB, Corey DP, Kramer P, Brin MF, Ozelius LJ, Breakefield XO. Leung JC, et al. Among authors: gasser t. Neurogenetics. 2001 Jul;3(3):133-43. doi: 10.1007/s100480100111. Neurogenetics. 2001. PMID: 11523564

2

The DYT1 gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-Jews.

Kramer PL, Heiman GA, Gasser T, Ozelius LJ, de Leon D, Brin MF, Burke RE, Hewett J, Hunt AL, Moskowitz C, et al. Kramer PL, et al. Among authors: gasser t. Am J Hum Genet. 1994 Sep;55(3):468-75. Am J Hum Genet. 1994. PMID: 8079990 Free PMC article.

3

Haplotype analysis at the DYT1 locus in Ashkenazi Jewish patients with occupational hand dystonia.

Gasser T, Bove CM, Ozelius LJ, Hallett M, Charness ME, Hochberg FH, Breakefield XO. Gasser T, et al. Mov Disord. 1996 Mar;11(2):163-6. doi: 10.1002/mds.870110208. Mov Disord. 1996. PMID: 8684386

4

The autosomal dominant dystonias.

Gasser T, Fahn S, Breakefield XO. Gasser T, et al. Brain Pathol. 1992 Oct;2(4):297-308. doi: 10.1111/j.1750-3639.1992.tb00707.x. Brain Pathol. 1992. PMID: 1341964 Review.

5

Genetic linkage studies in autosomal dominant parkinsonism: evaluation of seven candidate genes.

Gasser T, Wszolek ZK, Trofatter J, Ozelius L, Uitti RJ, Lee CS, Gusella J, Pfeiffer RF, Calne DB, Breakefield XO. Gasser T, et al. Ann Neurol. 1994 Sep;36(3):387-96. doi: 10.1002/ana.410360310. Ann Neurol. 1994. PMID: 7915897

6

GAG deletion in the DYT1 gene in early limb-onset idiopathic torsion dystonia in Germany.

Kamm C, Castelon-Konkiewitz E, Naumann M, Heinen F, Brack M, Nebe A, Ceballos-Baumann A, Gasser T. Kamm C, et al. Among authors: gasser t. Mov Disord. 1999 Jul;14(4):681-3. doi: 10.1002/1531-8257(199907)14:4<681::aid-mds1020>3.0.co;2-m. Mov Disord. 1999. PMID: 10435508

7

Search for the PARK3 founder haplotype in a large cohort of patients with Parkinson's disease from northern Germany.

Klein C, Vieregge P, Hagenah J, Sieberer M, Doyle E, Jacobs H, Gasser T, Breakefield XO, Risch NJ, Ozelius LJ. Klein C, et al. Among authors: gasser t. Ann Hum Genet. 1999 Jul;63(Pt 4):285-91. doi: 10.1046/j.1469-1809.1999.6340285.x. Ann Hum Genet. 1999. PMID: 10738540

8

Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystonia.

Walter M, Bonin M, Pullman RS, Valente EM, Loi M, Gambarin M, Raymond D, Tinazzi M, Kamm C, Glöckle N, Poths S, Gasser T, Bressman SB, Klein C, Ozelius LJ, Riess O, Grundmann K. Walter M, et al. Among authors: gasser t. Neurobiol Dis. 2010 May;38(2):192-200. doi: 10.1016/j.nbd.2009.12.019. Epub 2010 Jan 4. Neurobiol Dis. 2010. PMID: 20053375

9

The DYT1 GAG deletion is infrequent in sporadic and familial writer' s cramp.

Kamm C, Naumann M, Mueller J, Mai N, Riedel L, Wissel J, Gasser T. Kamm C, et al. Among authors: gasser t. Mov Disord. 2000 Nov;15(6):1238-41. doi: 10.1002/1531-8257(200011)15:6<1238::aid-mds1027>3.0.co;2-z. Mov Disord. 2000. PMID: 11104212

10

Genetic linkage studies in autosomal dominantly inherited L-DOPA responsive parkinsonism. Evaluation of candidate genes.

Gasser T, Wszolek Z, Supala A, Trofatter J, Ozelius L, Uitti RJ, Pfeiffer RF, Gusella J, Calne D, Breakefield XO. Gasser T, et al. Adv Neurol. 1996;69:87-95. Adv Neurol. 1996. PMID: 8615189 Clinical Trial. No abstract available.

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