𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Clinical spectrum of CADASIL: a study of 7 families

✍ Scribed by H Chabriat; K Vahedi; M.G Bousser; M.T Iba-Zizen; A Joutel; A Nibbio; T.G Nagy; E Tournier Lasserve; M.O Krebs; J Julien; X Ducrocq; M Levasseur; J.L Mas; B Dubois; P Homeyer; O Lyon-Caen


Book ID
118558586
Publisher
The Lancet
Year
1995
Tongue
English
Weight
879 KB
Volume
346
Category
Article
ISSN
0140-6736

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


CADASIL presenting with a movement disor
✍ Marcelo Miranda; Martin Dichgans; Andrea Slachevsky; Francisco Urbina; Ismael Me πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 265 KB

## Abstract Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary vascular disease that usually begins with migraine, followed by repeated strokes and progressive dementia. We describe an unusual clinical presentation of this condition

X-linked mental retardation: A study of
✍ Jacobs, Patricia A. ;Glover, Thomas W. ;Mayer, Martha ;Fox, Patricia ;Gerrard, J πŸ“‚ Article πŸ“… 1980 πŸ› John Wiley and Sons 🌐 English βš– 1002 KB

## Abstract Seven families with X‐linked mental retardation (MR) have been studied clinically and cytogenetically. All affected males in six of the families were found to have a fragile site on Xq in a number of their peripheral lymphocytes. The fragile site was not seen in any of the affected male