Dichgans M - Search Results

1

[CADASIL: clinical aspects and diagnosis].

Dichgans M, Gasser T. Dichgans M, et al. 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.

2

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. Neurology. 1999 Apr 22;52(7):1361-7. doi: 10.1212/wnl.52.7.1361. Neurology. 1999. PMID: 10227618

3

Cerebrospinal fluid findings in CADASIL.

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

4

[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: dichgans m. Nervenarzt. 1995 Dec;66(12):927-32. Nervenarzt. 1995. PMID: 8584078 German.

5

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. Genomics. 1996 Feb 15;32(1):151-4. doi: 10.1006/geno.1996.0094. Genomics. 1996. PMID: 8786108

6

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. Ann Neurol. 1998 Nov;44(5):731-9. doi: 10.1002/ana.410440506. Ann Neurol. 1998. PMID: 9818928

7

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: dichgans m. J Neurol. 1999 Jul;246(7):526-32. doi: 10.1007/s004150050398. J Neurol. 1999. PMID: 10463351

8

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. Eur J Hum Genet. 2000 Apr;8(4):280-5. doi: 10.1038/sj.ejhg.5200460. Eur J Hum Genet. 2000. PMID: 10854111

9

[Molecular diagnosis of hereditary neurologic diseases. Position paper].

Gasser T, Dichgans M, Jurkat-Rott K, Klockgether T, Klopstock T, Kretzschmar H, Lehmann-Horn F, Reichmann H, Rolfs A, Sander T, Stögbauer F. Gasser T, et al. Among authors: dichgans m. Nervenarzt. 2000 Oct;71(10):774-96. doi: 10.1007/s001150050665. Nervenarzt. 2000. PMID: 11082808 Review. German. No abstract available.

10

Reduced cerebrovascular CO(2) reactivity in CADASIL: A transcranial Doppler sonography study.

Pfefferkorn T, von Stuckrad-Barre S, Herzog J, Gasser T, Hamann GF, Dichgans M. Pfefferkorn T, et al. Among authors: dichgans m. Stroke. 2001 Jan;32(1):17-21. doi: 10.1161/01.str.32.1.17. Stroke. 2001. PMID: 11136908 Clinical Trial.

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