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Journal of Neuroinflammation, ISSN 1742-2094, 12/2009, Volume 6, Issue 1, pp. 38 - 38
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 03/2018, Volume 128, Issue 3, pp. 1141 - 1153
Dravet syndrome (DS) is a severe childhood-onset epilepsy commonly due to mutations of the sodium channel gene SCN1A. Patients with DS have a high risk of... 
MEDICINE, RESEARCH & EXPERIMENTAL | INHIBITORY INTERNEURONS | RISK-FACTORS | HEART-RATE-VARIABILITY | SODIUM-CHANNELS | UNEXPLAINED DEATH | MOUSE MODEL | EPILEPTIC SEIZURES | MECHANISMS | SUDDEN UNEXPECTED DEATH | SEROTONIN NEURONS | Humans | NAV1.1 Voltage-Gated Sodium Channel - genetics | Male | Receptors, Muscarinic - metabolism | Electroencephalography | Epilepsy - physiopathology | Hypoventilation - complications | Muscarinic Antagonists - pharmacology | Electrocardiography | Female | Electromyography | Child | Seizures | Respiration Disorders - pathology | Respiration Disorders - physiopathology | Bradycardia - physiopathology | Epilepsies, Myoclonic - physiopathology | Genotype | Parasympathetic Nervous System | Respiration, Artificial | Death, Sudden | Epilepsies, Myoclonic - complications | Mice, Inbred C3H | Epilepsy - complications | Hypoventilation - physiopathology | Animals | Video Recording | Mice | Mutation | Plethysmography | Respiration Disorders - complications | Complications and side effects | Respiratory insufficiency | Epilepsy | Sudden death | Patient outcomes | Risk factors | Genetic aspects | Seizures (Medicine) | Cardiac arrhythmia | Acetylcholine receptors (muscarinic) | Sleep disorders | Airway management | Apnea | Hypoxemia | Hypoventilation | Blood-brain barrier | Rodents | Sodium channels (voltage-gated) | Children | Heart diseases | Drug dosages | Sodium channels | Cardiac muscle | EEG | Heart rate | Bradycardia | Ventilation | Death | Respiration | Laboratory animals | Hyperthermia | Parasympathetic nervous system | Index Medicus | Abridged Index Medicus
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 8736 - 9
The ketogenic diet (KD) is an effective treatment option for intractable epilepsy. Here, we reviewed the last 10 years of our experience with the KD and... 
TRIAL | EFFICACY | MULTIDISCIPLINARY SCIENCES | INFANTS | GROWTH | Convulsions & seizures | Diet | Ketogenesis | Etiology | Epilepsy | Medical records | Infants | Drug resistance | Patients | Age
Journal Article
06/2014, ISBN 145113195X, 660
Whether you're new to electroencephalography or are looking to sharpen your EEG skills, this new 4th edition will be your go-to reference for EEG know-how.... 
Electroencephalography
eBook
Epilepsia, ISSN 0013-9580, 09/2012, Volume 53, Issue 9, pp. 1471 - 1480
Journal Article
Journal Article
Epileptic Disorders, ISSN 1294-9361, 09/2016, Volume 18, Issue 3, pp. 289 - 296
Aim . To describe the occurrence of epileptic spasms in epilepsy with myoclonic‐atonic seizures (EMAS) or Doose syndrome. Methods . Case descriptions of... 
drop‐attacks | Doose syndrome | epileptic spasms | myoclonic‐atonic seizures | Myoclonic-atonic seizures | Epileptic spasms | Drop-attacks | Seizures - physiopathology | Humans | Adolescent | Male | Electroencephalography | Muscle Weakness - physiopathology | Child | Syndrome | Myoclonus - physiopathology | Epilepsy | Index Medicus
Journal Article
2014, Fourth edition., ISBN 9781451131956
"Current Practice of Clinical Electroencephalography, 4e, covers the full range of applications of EEG and evoked potentials in contemporary neurophysiology.... 
methods | Electroencephalography
Web Resource
by Baldassari, Sara and Picard, Fabienne and Verbeek, Nienke E and van Kempen, Marjan and Brilstra, Eva H and Lesca, Gaetan and Conti, Valerio and Guerrini, Renzo and Bisulli, Francesca and Licchetta, Laura and Pippucci, Tommaso and Tinuper, Paolo and Hirsch, Edouard and de Saint Martin, Anne and Chelly, Jamel and Rudolf, Gabrielle and Chipaux, Mathilde and Ferrand-Sorbets, Sarah and Dorfmüller, Georg and Sisodiya, Sanjay and Balestrini, Simona and Schoeler, Natasha and Hernandez-Hernandez, Laura and Krithika, S and Oegema, Renske and Hagebeuk, Eveline and Gunning, Boudewijn and Deckers, Charles and Berghuis, Bianca and Wegner, Ilse and Niks, Erik and Jansen, Floor E and Braun, Kees and de Jong, Daniëlle and Rubboli, Guido and Talvik, Inga and Sander, Valentin and Uldall, Peter and Jacquemont, Marie-Line and Nava, Caroline and Leguern, Eric and Julia, Sophie and Gambardella, Antonio and d’Orsi, Giuseppe and Crichiutti, Giovanni and Faivre, Laurence and Darmency, Veronique and Benova, Barbora and Krsek, Pavel and Biraben, Arnaud and Lebre, Anne-Sophie and Jennesson, Mélanie and Sattar, Shifteh and Marchal, Cécile and Nordli, Douglas R and Lindstrom, Kristin and Striano, Pasquale and Lomax, Lysa Boissé and Kiss, Courtney and Bartolomei, Fabrice and Lepine, Anne Fabienne and Schoonjans, An-Sofie and Stouffs, Katrien and Jansen, Anna and Panagiotakaki, Eleni and Ricard-Mousnier, Brigitte and Thevenon, Julien and de Bellescize, Julitta and Catenoix, Hélène and Dorn, Thomas and Zenker, Martin and Müller-Schlüter, Karen and Brandt, Christian and Krey, Ilona and Polster, Tilman and Wolff, Markus and Balci, Meral and Rostasy, Kevin and Achaz, Guillaume and Zacher, Pia and Becher, Thomas and Cloppenborg, Thomas and Yuskaitis, Christopher J and Weckhuysen, Sarah and Poduri, Annapurna and Lemke, Johannes R and Møller, Rikke S and Baulac, Stéphanie
Genetics in Medicine, ISSN 1098-3600, 02/2019, Volume 21, Issue 2, pp. 398 - 408
Purpose: To define the phenotypic and mutational spectrum of epilepsies related to DEPDC5, NPRL2 and NPRL3 genes encoding the GATOR1 complex, a negative... 
Genetic focal epilepsy | mTORC1 pathway | Focal cortical dysplasia | SUDEP | DEPDC5 | FAMILIAL FOCAL EPILEPSY | MAMMALIAN TARGET | CORTICAL DYSPLASIA | COMPLEX | DEPDC5 MUTATIONS | MODEL | SUDDEN UNEXPECTED DEATH | GTPASES | GENETICS | GENES | GENETICS & HEREDITY | Convulsions & seizures | Epilepsy | Index Medicus | Life Sciences | Genetics | Human genetics | focal cortical dysplasia | genetic focal epilepsy
Journal Article