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Epilepsy Research and Treatment
|
September 8, 2012
Genetics of temporal lobe epilepsy: a review
Annick 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 disorder
Anthony Carrard, Annick Salzmann, Alain Malafosse, et al.
Epilepsia
|
July 19, 2011
Replication of association between a SCN1A splice variant and febrile seizures
François 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 study
Annick 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 polymorphism
Anthony Carrard, Annick Salzmann, Nader Perroud, et al.
Epilepsia
|
June 11, 2005
GABA receptor 1 polymorphism (G1465A) and temporal lobe epilepsy
Annick 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 epilepsy
Matthew 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 family
Samia 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 epilepsy
Matthew 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 family
Nejla Belhedi, Frédérique Bena, Amel Mrabet, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Epilepsy Research and Treatment
|
September 8, 2012
Genetics of temporal lobe epilepsy: a review
Annick 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 disorder
Anthony Carrard, Annick Salzmann, Alain Malafosse, et al.
Epilepsia
|
July 19, 2011
Replication of association between a SCN1A splice variant and febrile seizures
François 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 study
Annick 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 polymorphism
Anthony Carrard, Annick Salzmann, Nader Perroud, et al.
Epilepsia
|
June 11, 2005
GABA receptor 1 polymorphism (G1465A) and temporal lobe epilepsy
Annick 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 epilepsy
Matthew 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 family
Samia 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 epilepsy
Matthew 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 family
Nejla Belhedi, Frédérique Bena, Amel Mrabet, et al.
Page
of 2