E. Andermann

Best Publications

• Early childhood prolonged febrile convulsions, atrophy and sclerosis of mesial structures, and temporal lobe epilepsy: An MRI volumetric study

  F. Cendes;F. Andermann;F. Dubeau;P. Gloor

  560
  Citations

• Congenital malformations due to antiepileptic drugs

  S Kaneko;D Battino;E Andermann;K Wada

  533
  Citations

• Atrophy of mesial structures in patients with temporal lobe epilepsy: cause or consequence of repeated seizures?

  F. Cendes;F. Andermann;F. Andermann;P. Gloor;P. Gloor;I. Lopes-Cendes;I. Lopes-Cendes

  327
  Citations

• Autosomal Dominant Nocturnal Frontal-Lobe Epilepsy: Genetic Heterogeneity and Evidence for a Second Locus at 15q24

  H.A. Phillips;I.E. Scheffer;K.M. Crossland;K.P. Bhatia

  297
  Citations

• X-linked malformations of neuronal migration

  W. B. Dobyns;E. Andermann;F. Andermann;D. Czapansky-Beilman

  284
  Citations

• Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?

  R. Singh;E. Andermann;W. P. A. Whitehouse;A. S. Harvey

  281
  Citations

• MYOCLONUS EPILEPSY AND RAGGED-RED FIBRES (MERRF)1. A CLINICAL, PATHOLOGICAL, BIOCHEMICAL, MAGNETIC RESONANCE SPECTROGRAPHIC AND POSITRON EMISSION TOMOGRAPHIC STUDY

  S. F. Berkovic;S. Carpenter;A. Evans;G. Karpati

  276
  Citations

• Levetiracetam for the treatment of idiopathic generalized epilepsy with myoclonic seizures

  S. Noachtar;E. Andermann;P. Meyvisch;F. Andermann

  272
  Citations

• Sodium channel α1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms

  R. H. Wallace;B. L. Hodgson;B. E. Grinton;R. M. Gardiner

  241
  Citations

• Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome

  V. L. Sheen;A. Jansen;M. H. Chen;E. Parrini

  206
  Citations

• Excitatory amino acids are elevated in human epileptic cerebral cortex

  A. Sherwin;Y. Robitaille;F. Quesney;A. Olivier

  194
  Citations

• Surgical treatment of epilepsy in tuberous sclerosis: Strategic and results in 18 patients

  M. M. Guerreiro;F. Andermann;E. Andermann;A. Palmini

  177
  Citations

• Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment.

  M. M. Guerreiro;E. Andermann;R. Guerrini;W. B. Dobyns

  171
  Citations

• Familial Temporal Lobe Epilepsy: A Clinically Heterogeneous Syndrome

  F. Cendes;I. Lopes-Cendes;E. Andermann;F. Andermann

  168
  Citations

• Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis

  Katherine R. Smith;Hans Henrik M Dahl;Laura Canafoglia;Eva Andermann

  158
  Citations

• Pathophysiological Mechanisms of Dominant and Recessive GLRA1 Mutations in Hyperekplexia

  Seo-Kyung Chung;Jean-Francois Vanbellinghen;Jonathan G. L. Mullins;Angela Robinson

  155
  Citations

• Mutation spectrum and predicted function of laforin in Lafora's progressive myoclonus epilepsy.

  B. A. Minassian;L. Ianzano;M. Meloche;E. Andermann

  147
  Citations

• Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients

  I. Silveira;I. Lopes-Cendes;S. Kish;P. Maciel;P. Maciel

  146
  Citations

• Integrative cortical dysfunction and pervasive motion perception deficit in fragile X syndrome

  C. S. Kogan;A. Bertone;K. Cornish;I. Boutet

  144
  Citations

• Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene.

  J M Pinard;J Motte;C Chiron;R Brian

  143
  Citations