Gasser T - Search Results

1

Quantitative MRI in CADASIL: correlation with disability and cognitive performance.

Dichgans M, Filippi M, Brüning R, Iannucci G, Berchtenbreiter C, Minicucci L, Uttner I, Crispin A, Ludwig H, Gasser T, Yousry TA. Dichgans M, et al. Among authors: gasser t. Neurology. 1999 Apr 22;52(7):1361-7. doi: 10.1212/wnl.52.7.1361. Neurology. 1999. PMID: 10227618

2

The phenotypic spectrum of CADASIL: clinical findings in 102 cases.

Dichgans M, Mayer M, Uttner I, Brüning R, Müller-Höcker J, Rungger G, Ebke M, Klockgether T, Gasser T. Dichgans M, et al. Among authors: gasser t. Ann Neurol. 1998 Nov;44(5):731-9. doi: 10.1002/ana.410440506. Ann Neurol. 1998. PMID: 9818928

3

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.

4

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

5

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

6

[CADASIL: clinical aspects and diagnosis].

Dichgans M, Gasser T. Dichgans M, et al. Among authors: gasser t. Dtsch Med Wochenschr. 1998 Aug 14;123(33):979-81. doi: 10.1055/s-2007-1024107. Dtsch Med Wochenschr. 1998. PMID: 9739346 Review. German. No abstract available.

7

Small in-frame deletions and missense mutations in CADASIL: 3D models predict misfolding of Notch3 EGF-like repeat domains.

Dichgans M, Ludwig H, Müller-Höcker J, Messerschmidt A, Gasser T. Dichgans M, et al. Among authors: gasser t. Eur J Hum Genet. 2000 Apr;8(4):280-5. doi: 10.1038/sj.ejhg.5200460. Eur J Hum Genet. 2000. PMID: 10854111

8

[Hereditary CADASIL cerebral arteriopathy. Report of a family].

Mayer M, Dichgans M, Gasser T, Büttner U, Uttner I, Straube A. Mayer M, et al. Among authors: gasser t. Nervenarzt. 1995 Dec;66(12):927-32. Nervenarzt. 1995. PMID: 8584078 German.

9

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

10

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

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