Literature DB >> 9840354

A family with autosomal dominant nocturnal frontal lobe epilepsy and mental retardation.

R Khatami, M Neumann, H Schulz, H W Kölmel.   

Abstract

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Year:  1998        PMID： 9840354     DOI： 10.1007/s004150050291

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


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  4 in total

Review 1.  The sleep manifestations of frontal lobe epilepsy.

Authors:  Christopher P Derry
Journal:  Curr Neurol Neurosci Rep       Date:  2011-04       Impact factor: 5.081

2.  Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy.

Authors:  Sarah E Heron; Katherine R Smith; Melanie Bahlo; Lino Nobili; Esther Kahana; Laura Licchetta; Karen L Oliver; Aziz Mazarib; Zaid Afawi; Amos Korczyn; Giuseppe Plazzi; Steven Petrou; Samuel F Berkovic; Ingrid E Scheffer; Leanne M Dibbens
Journal:  Nat Genet       Date:  2012-10-21       Impact factor: 38.330

3.  PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy.

Authors:  Michael S Hildebrand; Rick Tankard; Elena V Gazina; John A Damiano; Kate M Lawrence; Hans-Henrik M Dahl; Brigid M Regan; Aiden Eliot Shearer; Richard J H Smith; Carla Marini; Renzo Guerrini; Angelo Labate; Antonio Gambardella; Paolo Tinuper; Laura Lichetta; Sara Baldassari; Francesca Bisulli; Tommaso Pippucci; Ingrid E Scheffer; Christopher A Reid; Steven Petrou; Melanie Bahlo; Samuel F Berkovic
Journal:  Ann Clin Transl Neurol       Date:  2015-07-03       Impact factor: 4.511

Review 4.  Sleep-related hypermotor epilepsy: prevalence, impact and management strategies.

Authors:  Veronica Menghi; Francesca Bisulli; Paolo Tinuper; Lino Nobili
Journal:  Nat Sci Sleep       Date:  2018-10-10
  4 in total

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