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A Ducros

Showing results (31-40 of 64) with videos related to

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Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Implications of prenatal diagnosis of sickle cell diseaseM de Montalembert, M Guilloud-Bataille, A Ducros, et al.
Neurology|February 11, 2000
Decreased hemispheric water mobility in hemiplegic migraine related to mutation of CACNA1A geneH Chabriat, K Vahedi, C A Clark, et al.
Neuropediatrics|November 24, 1999
Recurrent episodes of coma: an unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1B Echenne, A Ducros, F Rivier, et al.
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.
Revue Neurologique|June 22, 2014
[French guidelines for diagnosis and treatment of cluster headache (French Headache Society)]A Donnet, G Demarquay, A Ducros, 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.
Pageof 7

Showing results (31-40 of 64) with videos related to

Sort By:
Pageof 7
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Implications of prenatal diagnosis of sickle cell diseaseM de Montalembert, M Guilloud-Bataille, A Ducros, et al.
Neurology|February 11, 2000
Decreased hemispheric water mobility in hemiplegic migraine related to mutation of CACNA1A geneH Chabriat, K Vahedi, C A Clark, et al.
Neuropediatrics|November 24, 1999
Recurrent episodes of coma: an unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1B Echenne, A Ducros, F Rivier, et al.
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.
Revue Neurologique|June 22, 2014
[French guidelines for diagnosis and treatment of cluster headache (French Headache Society)]A Donnet, G Demarquay, A Ducros, 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.
Pageof 7