Gerhard Kluger

Overview

Best Publications

• Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.

  Markus Wolff;Katrine M Johannesen;Ulrike B S Hedrich;Silvia Masnada

  570
  Citations

• Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology

  Alexis Arzimanoglou;Jacqueline French;Warren T. Blume;J. Helen Cross

  553
  Citations

• Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

  Johannes R Lemke;Dennis Lal;Eva M Reinthaler;Isabelle Steiner

  501
  Citations

• Rufinamide for generalized seizures associated with Lennox–Gastaut syndrome

  T. Glauser;G. Kluger;R. Sachdeo;G. Krauss

  433
  Citations

• Febrile infection-related epilepsy syndrome (FIRES): pathogenesis, treatment, and outcome: a multicenter study on 77 children.

  Uri Kramer;Ching Shiang Chi;Kuang Lin Lin;Nicola Specchio

  379
  Citations

• STXBP1 encephalopathy A neurodevelopmental disorder including epilepsy

  Hannah Stamberger;Marina Nikanorova;Marjolein H. Willemsen;Patrizia Accorsi

  335
  Citations

• The phenotypic spectrum of SCN8A encephalopathy

  Jan Larsen;Gemma L Carvill;Elena Gardella;Gerhard Kluger

  300
  Citations

• Febrile infection-related epilepsy syndrome (FIRES): a nonencephalitic encephalopathy in childhood.

  Andreas Van Baalen;Martin Häusler;Rainer Boor;Axel Rohr

  286
  Citations

• De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome

  Arvid Suls;Johanna A. Jaehn;Angela Kecskés;Yvonne Weber

  263
  Citations

• Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy

  Cyril Mignot;Celina von Stülpnagel;Caroline Nava;Dorothée Ville

  213
  Citations

• Febrile Infection-Related Epilepsy Syndrome: Clinical Review and Hypotheses of Epileptogenesis.

  Andreas van Baalen;Annamaria Vezzani;Martin Häusler;Gerhard Kluger

  156
  Citations

• Adjunctive rufinamide in Lennox-Gastaut syndrome: a long-term, open-label extension study.

  G. Kluger;T. Glauser;G. Krauss;R. Seeruthun

  144
  Citations

• Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease.

  Sara Zagaglia;Sara Zagaglia;Christina Selch;Jelena Radic Nisevic;Davide Mei

  142
  Citations

• DEPDC5 mutations in genetic focal epilepsies of childhood

  Dennis Lal;Eva M. Reinthaler;Julian Schubert;Hiltrud Muhle

  133
  Citations

• Mutations in GABRB3: From febrile seizures to epileptic encephalopathies

  Rikke S Møller;Thomas V Wuttke;Ingo Helbig;Carla Marini

  122
  Citations

• Effectiveness and Tolerability of Perampanel in Children and Adolescents with Refractory Epilepsies: First Experiences

  Anna Biró;Ulrich Stephani;Tiziana Tarallo;Thomas Bast

  119
  Citations

• Valproic acid-induced hepatopathy: nine new fatalities in Germany from 1994 to 2003.

  Stephan A. Koenig;Deike Buesing;Elke Longin;Randi Oehring

  117
  Citations

• 47 patients with FLNA associated periventricular nodular heterotopia

  Max Lange;Burkhard Kasper;Axel Bohring;Frank Rutsch

  116
  Citations

• Heterotopic ossification in childhood and adolescence.

  Gerhard Kluger;Andreas Kochs;Hans Holthausen

  110
  Citations

• Co-occurring malformations of cortical development and SCN1A gene mutations

  Carmen Barba;Elena Parrini;Roland Coras;Anna Galuppi

  106
  Citations

• Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU

  Christel Depienne;Caroline Nava;Boris Keren;Solveig Heide

  91
  Citations