PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy-Reference-Cited by-同舟云学术

PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy

Published:2015-07-03 Issue:8 Volume:2 Page:821-830
ISSN:2328-9503
Container-title:Annals of Clinical and Translational Neurology
language:en
Short-container-title:Ann Clin Transl Neurol

Author:

Hildebrand Michael S.¹,Tankard Rick²,Gazina Elena V.³,Damiano John A.¹,Lawrence Kate M.¹,Dahl Hans‐Henrik M.¹,Regan Brigid M.¹,Shearer Aiden Eliot⁴,Smith Richard J. H.⁴,Marini Carla⁵,Guerrini Renzo⁵,Labate Angelo⁶⁷,Gambardella Antonio⁶⁷,Tinuper Paolo⁸,Lichetta Laura⁸,Baldassari Sara⁸,Bisulli Francesca⁸,Pippucci Tommaso⁸,Scheffer Ingrid E.¹⁹,Reid Christopher A.³,Petrou Steven³,Bahlo Melanie²,Berkovic Samuel F.¹

Affiliation:

1. Epilepsy Research Centre Department of Medicine Austin Health University of Melbourne Melbourne Victoria Australia

2. Bioinformatics Division The Walter and Eliza Hall Institute Melbourne Victoria Australia

3. The Florey Institute for Neuroscience and Mental Health The University of Melbourne Melbourne Victoria Australia

4. Molecular Otolaryngology & Renal Research Laboratories Department of Otolaryngology‐Head and Neck Surgery University of Iowa Hospitals and Clinics Iowa City Iowa

5. Pediatric Neurology and Neurogenetics Unit and Laboratories A. Meyer Children's Hospital‐University of Florence Florence Italy

6. Institute of Neurology University Magna Græcia Catanzaro Italy

7. Institute of Molecular Bioimaging and Physiology of the National Research Council (IBFM‐CNR) Germaneto CZ Italy

8. Medical Genetics Unit Polyclinic Sant'Orsola‐Malpighi and Department of Medical and Surgical Sciences University of Bologna Bologna Italy

9. Department of Paediatrics Royal Children's Hospital University of Melbourne Melbourne Victoria Australia

Funder

National Health and Medical Research Council (NHMRC)

Australian Research Council (ARC)

Victorian State Government Operational Infrastructure Support

Australian Government NHMRC IRIISS

Telethon Foundation

Publisher

Wiley

Subject

Clinical Neurology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.224

Reference35 articles.

1. Autosomal dominant nocturnal frontal lobe epilepsy

2. Distinguishing Sleep Disorders From Seizures

3. A Korean Kindred With Autosomal Dominant Nocturnal Frontal Lobe Epilepsy and Mental Retardation

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

5. Increased Sensitivity of the Neuronal Nicotinic Receptor α2 Subunit Causes Familial Epilepsy with Nocturnal Wandering and Ictal Fear

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