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Annick Salzmann

Showing results (1-10 of 14) with videos related to

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Epilepsy Research and Treatment|September 8, 2012
Genetics of temporal lobe epilepsy: a reviewAnnick Salzmann, Alain Malafosse
Journal of Affective Disorders|April 2, 2011
Increased DNA methylation status of the serotonin receptor 5HTR1A gene promoter in schizophrenia and bipolar disorderAnthony Carrard, Annick Salzmann, Alain Malafosse, et al.
Epilepsia|July 19, 2011
Replication of association between a SCN1A splice variant and febrile seizuresFrançois Le Gal, Annick Salzmann, Arielle Crespel, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 11, 2008
Candidate genes for temporal lobe epilepsy: a replication studyAnnick Salzmann, Nader Perroud, Arielle Crespel, et al.
Brain and Behavior|March 9, 2012
Genetic association of the Phosphoinositide-3 kinase in schizophrenia and bipolar disorder and interaction with a BDNF gene polymorphismAnthony Carrard, Annick Salzmann, Nader Perroud, et al.
Epilepsia|June 11, 2005
GABA receptor 1 polymorphism (G1465A) and temporal lobe epilepsyAnnick Salzmann, Bruno Moulard, Arielle Crespel, et al.
Plos One|April 16, 2015
Novel carboxypeptidase A6 (CPA6) mutations identified in patients with juvenile myoclonic and generalized epilepsyMatthew R Sapio, Monique Vessaz, Pierre Thomas, et al.
Epilepsy Research|April 10, 2010
Genetic linkage study of an autosomal recessive form of juvenile myoclonic epilepsy in a consanguineous Tunisian familySamia Layouni, Annick Salzmann, Michel Guipponi, et al.
The Journal of Biological Chemistry|October 30, 2012
Naturally occurring carboxypeptidase A6 mutations: effect on enzyme function and association with epilepsyMatthew R Sapio, Annick Salzmann, Monique Vessaz, et al.
BMC Genetics|September 27, 2013
A new locus on chromosome 22q13.31 linked to recessive genetic epilepsy with febrile seizures plus (GEFS+) in a Tunisian consanguineous familyNejla Belhedi, Frédérique Bena, Amel Mrabet, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Epilepsy Research and Treatment|September 8, 2012
Genetics of temporal lobe epilepsy: a reviewAnnick Salzmann, Alain Malafosse
Journal of Affective Disorders|April 2, 2011
Increased DNA methylation status of the serotonin receptor 5HTR1A gene promoter in schizophrenia and bipolar disorderAnthony Carrard, Annick Salzmann, Alain Malafosse, et al.
Epilepsia|July 19, 2011
Replication of association between a SCN1A splice variant and febrile seizuresFrançois Le Gal, Annick Salzmann, Arielle Crespel, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 11, 2008
Candidate genes for temporal lobe epilepsy: a replication studyAnnick Salzmann, Nader Perroud, Arielle Crespel, et al.
Brain and Behavior|March 9, 2012
Genetic association of the Phosphoinositide-3 kinase in schizophrenia and bipolar disorder and interaction with a BDNF gene polymorphismAnthony Carrard, Annick Salzmann, Nader Perroud, et al.
Epilepsia|June 11, 2005
GABA receptor 1 polymorphism (G1465A) and temporal lobe epilepsyAnnick Salzmann, Bruno Moulard, Arielle Crespel, et al.
Plos One|April 16, 2015
Novel carboxypeptidase A6 (CPA6) mutations identified in patients with juvenile myoclonic and generalized epilepsyMatthew R Sapio, Monique Vessaz, Pierre Thomas, et al.
Epilepsy Research|April 10, 2010
Genetic linkage study of an autosomal recessive form of juvenile myoclonic epilepsy in a consanguineous Tunisian familySamia Layouni, Annick Salzmann, Michel Guipponi, et al.
The Journal of Biological Chemistry|October 30, 2012
Naturally occurring carboxypeptidase A6 mutations: effect on enzyme function and association with epilepsyMatthew R Sapio, Annick Salzmann, Monique Vessaz, et al.
BMC Genetics|September 27, 2013
A new locus on chromosome 22q13.31 linked to recessive genetic epilepsy with febrile seizures plus (GEFS+) in a Tunisian consanguineous familyNejla Belhedi, Frédérique Bena, Amel Mrabet, et al.
Pageof 2