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Neurology|November 14, 2001
NOTCH3 mutation involving three cysteine residues in a family with typical CADASILM Dichgans, J Herzog, T GasserGenomics|February 15, 1996
Identification of a key recombinant narrows the CADASIL gene region to 8 cM and argues against allelism of CADASIL and familial hemiplegic migraineM Dichgans, M Mayer, B Müller-Myhsok, et al.European Journal of Human Genetics : EJHG|June 15, 2000
Small in-frame deletions and missense mutations in CADASIL: 3D models predict misfolding of Notch3 EGF-like repeat domainsM Dichgans, H Ludwig, J Müller-Höcker, et al.Der Nervenarzt|December 1, 1995
[Hereditary CADASIL cerebral arteriopathy. Report of a family]M Mayer, M Dichgans, T Gasser, et al.Radiology|February 13, 2001
Differential lesion patterns in CADASIL and sporadic subcortical arteriosclerotic encephalopathy: MR imaging study with statistical parametric group comparisonD P Auer, B Pütz, C Gössl, et al.Stroke|January 4, 2001
Reduced cerebrovascular CO(2) reactivity in CADASIL: A transcranial Doppler sonography studyT Pfefferkorn, S von Stuckrad-Barre, J Herzog, et al.Acta Neurologica Scandinavica|June 1, 1997
CADASIL: skin biopsy allows diagnosis in early stagesM Ebke, M Dichgans, M Bergmann, et al.Sleep|August 18, 2000
Clinical characteristics and frequency of the hereditary restless legs syndrome in a population of 300 patientsJ Winkelmann, T C Wetter, V Collado-Seidel, et al.Neurology|July 26, 2006
RLS3: fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneityK M Liebetanz, J Winkelmann, C Trenkwalder, et al.Stroke|March 10, 2001
Correlations between clinical findings and magnetization transfer imaging metrics of tissue damage in individuals with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyG Iannucci, M Dichgans, M Rovaris, et al.Pageof 60