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Neurology|November 4, 2000
CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophyK Vahedi, C Denier, A Ducros, et al.
Annals of Neurology|March 1, 1995
A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19pK Vahedi, A Joutel, P Van Bogaert, et al.
American Journal of Human Genetics|December 1, 1994
Genetic heterogeneity of familial hemiplegic migraineA Joutel, A Ducros, K Vahedi, et al.
The New England Journal of Medicine|July 7, 2001
The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channelA Ducros, C Denier, A Joutel, et al.
Genomics|December 1, 1996
A human homolog of bacterial acetolactate synthase genes maps within the CADASIL critical regionA Joutel, A Ducros, S Alamowitch, et al.
Biochemistry|May 19, 2004
Structural studies of the beta-glycosidase from Sulfolobus solfataricus in complex with covalently and noncovalently bound inhibitorsTracey M Gloster, Shirley Roberts, Valérie M-A Ducros, et al.
Revue Neurologique|January 14, 2014
Subarachnoid and intra-cerebral hemorrhage in young adults: rare and underdiagnosedB Mathon, A Ducros, D Bresson, et al.
The Journal of Biological Chemistry|September 29, 2004
The use of forced protein evolution to investigate and improve stability of family 10 xylanases. The production of Ca2+-independent stable xylanasesSimon R Andrews, Edward J Taylor, Gavin Pell, et al.
European Journal of Neurology|August 19, 2020
Acute retinal arterial ischaemia: silent brain infarcts prevalence and short-term recurrenceX Ayrignac, C Zagroun, A Coget, et al.
Chemical Communications (Cambridge, England)|July 5, 2003
Expansion of the glycosynthase repertoire to produce defined manno-oligosaccharidesMichael Jahn, Dominik Stoll, R Antony J Warren, et al.
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