Inventaire - your friends and communities are your best library

Fever, genes, and epilepsy

author

Stéphanie Baulac

1975 -

Michel Baulac

published in: Lancet Neurology

date of publication: 2004-07-01

Cites articles 120

Date

Title

Authors

2004-04-01

Monogenic idiopathic epilepsies

Alexis Brice, Michel Baulac
2004-02-01

Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations

Davide Mei, Francesca Moro, Elena Parrini, Sarah E Heron, Federico Zara, Renzo Guerrini, Daniela Buti, Pierangelo Veggiotti, Anna Volzone
2004-02-01

Mutations of neuronal voltage-gated Na+ channel alpha 1 subunit gene SCN1A in core severe myoclonic epilepsy in infancy (SMEI) and in borderline SMEI (SMEB)

Shinichi Hirose
2003-02-01

Phenotypic features of familial febrile seizures: case-control study
2003-06-01

Failure to find causal mutations in the GABA(A)-receptor gamma2 subunit (GABRG2) gene in Japanese febrile seizure patients
2003-04-01

The lack of association between febrile convulsions and polymorphisms in SCN1A

Chao-Ching Huang
2003-02

Functional characterization of the D188V mutation in neuronal voltage-gated sodium channel causing generalized epilepsy with febrile seizures plus (GEFS)

Guy A. Rouleau, Patrick Cossette
2003-06-24

Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy

Elena Fontana, Federico Zara, Enrico Bertini, Federico Vigevano, Bernardo Dalla Bernardina
2003-03-01

Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures
2003-09-01

Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus

Antonio Gambardella, Angelo Labate, Angela Aurora Pasqua, Donatella Civitelli, Elvira Valeria De Marco, Umberto Aguglia, Aldo Quattrone, Grazia Annesi, Patrizia Tarantino, Sara Carrideo, Mario Zappia
2003-09-23

A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy

Christine Van Broeckhoven
2003-01-01

Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutation,Childhood absence epilepsy and febrile seizures: a family with a GABAA receptor mutation

Carla Marini, Ingrid Scheffer, Samuel Berkovic
2003

Generalized epilepsy with febrile seizures plus type 2 mutation W1204R alters voltage-dependent gating of Na(v)1.1 sodium channels

Alan Goldin
2003-09-01

Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms

Robyn Wallace, Ingrid Scheffer, Leanne Dibbens
2003-03-01

No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy

Maurizio Elia, Anna Rita Ferrari, Elena Fontana, Tiziana Granata, Margherita Santucci, Federico Zara, Bernardo Dalla Bernardina
2003-03-01

Severe infantile epilepsies: molecular genetics challenge clinical classification.

Ingrid Scheffer
2003-01-28

Febrile seizures and mesial temporal sclerosis: No association in a long-term follow-up study
2003-06-01

Increased frequency of interleukin-1beta-511T allele in patients with temporal lobe epilepsy, hippocampal sclerosis, and prolonged febrile convulsion.
2003-11-01

Surgical outcome in mesial temporal sclerosis correlates with prion protein gene variant.

Lauro Wichert-Ana, Vilma R Martins
2003-02-01

GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy

Antonio Gambardella
2003-09-01

Prodynorphin gene promoter polymorphism and temporal lobe epilepsy

Antonio Gambardella, Ida Manna, Angelo Labate, Umberto Aguglia, Aldo Quattrone, Mario Zappia
2003-10-01

Association Analysis of a Polymorphism of Interleukin 1β (IL‐1β) Gene with Temporal Lobe Epilepsy in a Chinese Population
2003-02-01

Prodynorphin gene promoter polymorphism and temporal lobe epilepsy

Peter Propping
2003-06-01

Mutation analysis of the leucine-rich, glioma inactivated 1 gene (LGI1) in Japanese febrile seizure patients
2003-02-01

Hippocampal atrophy and T2-weighted signal changes in familial mesial temporal lobe epilepsy.

Fernando Cendes
2003-10-01

Paroxysms of excitement: sodium channel dysfunction in heart and brain
2003-04

Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies

Holger Lerche, Snezana Maljevic, Peter Propping, Christian Kubisch, Gerhard Müller-Newen, Alexi K Alekov, Christoph Fahlke, Alfredo Ramirez, Steve Horvath
2003-10-01

Cold induces shifts of voltage dependence in mutant SCN4A, causing hypokalemic periodic paralysis
2002-01

Febrile Seizures
2002-12-01

A locus for simple pure febrile seizures maps to chromosome 6q22-q24.
2002-05-01

Lack of SCN1A mutations in familial febrile seizures

Federico Zara, Giuseppe Gobbi, Bernardo Dalla Bernardina
2002-01

Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1A

Kazuhiro Yamakawa, Hidehiko Okazawa

Article - wd:Q35811060

Welcome to Inventaire

the library of your friends and communities

learn more