Gasser T - Search Results

1

A susceptibility locus for Parkinson's disease maps to chromosome 2p13.

Gasser T, Müller-Myhsok B, Wszolek ZK, Oehlmann R, Calne DB, Bonifati V, Bereznai B, Fabrizio E, Vieregge P, Horstmann RD. Gasser T, et al. Nat Genet. 1998 Mar;18(3):262-5. doi: 10.1038/ng0398-262. Nat Genet. 1998. PMID: 9500549

2

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.

3

Linkage studies in alcohol-responsive myoclonic dystonia.

Gasser T, Bereznai B, Müller B, Pruszak-Seel R, Damrich R, Deuschl G, Oertel WH. Gasser T, et al. Mov Disord. 1996 Jul;11(4):363-70. doi: 10.1002/mds.870110403. Mov Disord. 1996. PMID: 8813214

4

The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease.

Gasser T, Müller-Myhsok B, Supala A, Zimmer E, Wieditz G, Wszolek ZK, Vieregge P, Bonifati V, Oertel WH. Gasser T, et al. J Neurol Neurosurg Psychiatry. 1996 Nov;61(5):518-20. doi: 10.1136/jnnp.61.5.518. J Neurol Neurosurg Psychiatry. 1996. PMID: 8937349 Free PMC article.

5

A novel SOD1 mutation in an Austrian family with amyotrophic lateral sclerosis.

Bereznai B, Winkler A, Borasio GD, Gasser T. Bereznai B, et al. Among authors: gasser t. Neuromuscul Disord. 1997 Mar;7(2):113-6. doi: 10.1016/s0960-8966(96)00419-1. Neuromuscul Disord. 1997. PMID: 9131652

6

Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD).

Vaughan JR, Farrer MJ, Wszolek ZK, Gasser T, Durr A, Agid Y, Bonifati V, DeMichele G, Volpe G, Lincoln S, Breteler M, Meco G, Brice A, Marsden CD, Hardy J, Wood NW. Vaughan JR, et al. Among authors: gasser t. Hum Mol Genet. 1998 Apr;7(4):751-3. doi: 10.1093/hmg/7.4.751. Hum Mol Genet. 1998. PMID: 9499430

7

Genetic complexity and Parkinson's disease.

Gasser T, Müller-Myhsok B, Wszolek ZK, Dürr A, Vaughan JR, Bonifati V, Meco G, Bereznai B, Oehlmann R, Agid Y, Brice A, Wood N. Gasser T, et al. Science. 1997 Jul 18;277(5324):388-9; author reply 389. Science. 1997. PMID: 9518367 No abstract available.

8

Phenotypic expression of the DYT1 mutation: a family with writer's cramp of juvenile onset.

Gasser T, Windgassen K, Bereznai B, Kabus C, Ludolph AC. Gasser T, et al. Ann Neurol. 1998 Jul;44(1):126-8. doi: 10.1002/ana.410440119. Ann Neurol. 1998. PMID: 9667600

9

Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome.

Zimprich A, Grabowski M, Asmus F, Naumann M, Berg D, Bertram M, Scheidtmann K, Kern P, Winkelmann J, Müller-Myhsok B, Riedel L, Bauer M, Müller T, Castro M, Meitinger T, Strom TM, Gasser T. Zimprich A, et al. Among authors: gasser t. Nat Genet. 2001 Sep;29(1):66-9. doi: 10.1038/ng709. Nat Genet. 2001. PMID: 11528394

10

Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes.

West AB, Zimprich A, Lockhart PJ, Farrer M, Singleton A, Holtom B, Lincoln S, Hofer A, Hill L, Müller-Myhsok B, Wszolek ZK, Hardy J, Gasser T. West AB, et al. Among authors: gasser t. Eur J Hum Genet. 2001 Sep;9(9):659-66. doi: 10.1038/sj.ejhg.5200698. Eur J Hum Genet. 2001. PMID: 11571553

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