Gasser T - Search Results

1

RLS3: fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity.

Liebetanz KM, Winkelmann J, Trenkwalder C, Pütz B, Dichgans M, Gasser T, Müller-Myhsok B. Liebetanz KM, et al. Among authors: gasser t. Neurology. 2006 Jul 25;67(2):320-1. doi: 10.1212/01.wnl.0000224886.65213.b5. Neurology. 2006. PMID: 16864828

2

Clinical symptoms and possible anticipation in a large kindred of familial restless legs syndrome.

Trenkwalder C, Seidel VC, Gasser T, Oertel WH. Trenkwalder C, et al. Among authors: gasser t. Mov Disord. 1996 Jul;11(4):389-94. doi: 10.1002/mds.870110407. Mov Disord. 1996. PMID: 8813218

3

Inherited Myoclonus-dystonia syndrome: narrowing the 7q21-q31 locus in German families.

Asmus F, Zimprich A, Naumann M, Berg D, Bertram M, Ceballos-Baumann A, Pruszak-Seel R, Kabus C, Dichgans M, Fuchs S, Müller-Myhsok B, Gasser T. Asmus F, et al. Among authors: gasser t. Ann Neurol. 2001 Jan;49(1):121-4. doi: 10.1002/1531-8249(200101)49:1<121::aid-ana20>3.0.co;2-8. Ann Neurol. 2001. PMID: 11198282

4

NOTCH3 mutation involving three cysteine residues in a family with typical CADASIL.

Dichgans M, Herzog J, Gasser T. Dichgans M, et al. Among authors: gasser t. Neurology. 2001 Nov 13;57(9):1714-7. doi: 10.1212/wnl.57.9.1714. Neurology. 2001. PMID: 11706120

5

Autosomal dominant parkinsonism associated with variable synuclein and tau pathology.

Wszolek ZK, Pfeiffer RF, Tsuboi Y, Uitti RJ, McComb RD, Stoessl AJ, Strongosky AJ, Zimprich A, Müller-Myhsok B, Farrer MJ, Gasser T, Calne DB, Dickson DW. Wszolek ZK, et al. Among authors: gasser t. Neurology. 2004 May 11;62(9):1619-22. doi: 10.1212/01.wnl.0000125015.06989.db. Neurology. 2004. PMID: 15136696

6

Spinocerebellar ataxia type 6: evidence for a strong founder effect among German families.

Dichgans M, Schöls L, Herzog J, Stevanin G, Weirich-Schwaiger H, Rouleau G, Bürk K, Klockgether T, Zühlke C, Laccone F, Riess O, Gasser T. Dichgans M, et al. Among authors: gasser t. Neurology. 1999 Mar 10;52(4):849-51. doi: 10.1212/wnl.52.4.849. Neurology. 1999. PMID: 10078738

7

Cerebrospinal fluid findings in CADASIL.

Dichgans M, Wick M, Gasser T. Dichgans M, et al. Among authors: gasser t. Neurology. 1999 Jul 13;53(1):233. doi: 10.1212/wnl.53.1.233. Neurology. 1999. PMID: 10408571 No abstract available.

8

Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL.

Mayer M, Straube A, Bruening R, Uttner I, Pongratz D, Gasser T, Dichgans M, Müller-Höcker J. Mayer M, et al. Among authors: gasser t. J Neurol. 1999 Jul;246(7):526-32. doi: 10.1007/s004150050398. J Neurol. 1999. PMID: 10463351

9

Clinical characteristics and frequency of the hereditary restless legs syndrome in a population of 300 patients.

Winkelmann J, Wetter TC, Collado-Seidel V, Gasser T, Dichgans M, Yassouridis A, Trenkwalder C. Winkelmann J, et al. Among authors: gasser t. Sleep. 2000 Aug 1;23(5):597-602. Sleep. 2000. PMID: 10947027

10

Identification of a key recombinant narrows the CADASIL gene region to 8 cM and argues against allelism of CADASIL and familial hemiplegic migraine.

Dichgans M, Mayer M, Müller-Myhsok B, Straube A, Gasser T. Dichgans M, et al. Among authors: gasser t. Genomics. 1996 Feb 15;32(1):151-4. doi: 10.1006/geno.1996.0094. Genomics. 1996. PMID: 8786108

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