Splice site mutation causing a seven amino acid <i>Notch3</i> in-frame deletion in CADASIL

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

Anne Joutel, Christophe Corpechot, Anne Ducros et al. · Nature · 1996 · 2.1K citations

Life Sciences, Genetics, Neurology +14

The phenotypic spectrum of CADASIL: Clinical findings in 102 cases

Martin Dichgans, M. Mayer, Ingo Uttner et al. · Annals of Neurology · 1998 · 734 citations

Medicine, Neurology, Neuroscience +13

Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients

Anne Joutel, Katayoun Vahedi, Christophe Corpechot et al. · The Lancet · 1997 · 684 citations

Life Sciences, Genetics, Molecular Genetics +13

Clinical spectrum of CADASIL: a study of 7 families

Hugues Chabriat, Katayoun Vahedi, M G Bousser et al. · The Lancet · 1995 · 674 citations

Medicine, Pathology, Clinical Medicine +2

Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

M M Ruchoux, Djelloul Guerouaou, B Vandenhaute et al. · Acta Neuropathologica · 1995 · 326 citations

Life Sciences, Neurology, Neuroscience +13