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2. List of Contributors

Author

Aaen, Gregory, primary, Abroms, Israel F., additional, Ådén, Ulrika, additional, Ahlsten, Gunnar, additional, Aird, Robert B., additional, Al-Zaidy, Samiah A., additional, Andermann, Fred, additional, Anlar, Banu, additional, Arzimanoglou, Alexis, additional, Ashwal, Stephen, additional, Augustine, Erika, additional, Ballaban-Gil, Karen, additional, Bamford, Nigel S., additional, Barlow, Charles F., additional, Bast, Thomas, additional, Bates, David, additional, Baumann, Robert J., additional, Bertini, Enrico, additional, Beya, Alidor, additional, Blaw, Michael, additional, Bodensteiner, John, additional, Bonthius, Daniel J., additional, Brin, Amy E., additional, Brockmann, Knut, additional, Brown, John Keith, additional, Brown, Stuart B., additional, Brumback, Audrey Christine, additional, Bureau, Michelle, additional, Burke, James R., additional, Bye, Annie, additional, Camfield, Carol, additional, Camfield, Peter, additional, Campistol Plana, Jaume, additional, Canale, Dee James, additional, Caneris, Onasis, additional, Caraballo, Roberto H., additional, Caviness, Alison Chantal, additional, Chao, Hsiao-Tuan, additional, Chapman, Catherine A., additional, Chaves-Carballo, Enrique, additional, Cho, Yoon-Jae, additional, Christen, Hans-Jürgen, additional, Chugani, Harry T., additional, Cioni, Giovanni, additional, Clark, David, additional, Cliff, Edward Robert Scheffer, additional, Cochran, Frederick B., additional, Cohen, Bruce H., additional, Cohen, Maynard M., additional, Collins, Kevin, additional, Covanis, Athanasios, additional, Critchley, Macdonald, additional, Cross, J. Helen, additional, Crumrine, Patricia K., additional, Curatolo, Paolo, additional, Davies, Pamela A., additional, deVeber, Gabrielle, additional, De Vivo, Darryl C., additional, de Vries, Linda S., additional, De Waele, Liesbeth, additional, DeMyer, William, additional, Devlin, Anita, additional, Dobyns, William B., additional, Dodson, W. Edwin, additional, Donald, Kirsty, additional, Duffy, Frank H., additional, Dunn, David W., additional, Dunn, Henry G., additional, Dure, Leon S., additional, Dyken, Paul Richard, additional, Encha-Razavi, Férechté, additional, Erenberg, Gerald, additional, Estes, Melinda L., additional, Evrard, Philippe, additional, Ferriero, Donna, additional, Ferry, Peggy, additional, Fine, Archie, additional, Fine, Edward J., additional, Fine, John S., additional, Finkel, Richard S., additional, Fischer, Alain, additional, Fischer, Christine, additional, Fogan, Lance, additional, Fowler, Glenn W., additional, Frank, Yitzchak, additional, Fullerton, Heather J., additional, Furukawa, Tetsuo, additional, Gabriel, Ronald S., additional, Galanopoulou, Aristea S., additional, Gardner-Medwin, David, additional, Garg, Bhuwan, additional, Genton, Pierre, additional, George, Mark S., additional, Gineste, Thierry, additional, Giza, Christopher C., additional, Goemans, Nathalie, additional, Golden, Gerald S., additional, Golden, Jeffrey Alan, additional, Goldstein, Gary W., additional, Gomez, Christopher, additional, Gomez, Manuel R., additional, Gomez, Timothy, additional, Goodkin, Howard P., additional, Gordon, Neil, additional, Gressens, Pierre, additional, Groger, Helmut, additional, Guerrini, Renzo, additional, Gurnett, Christina A., additional, Gussoni, Emanuela, additional, Haas, Richard, additional, Hagberg, Bengt, additional, Haller, Jerome S., additional, Hartman, Adam L., additional, Haruda, Fred, additional, Hirtz, Deborah, additional, Hogan, Gwendolyn R., additional, Hunt, Guy M., additional, Iannaccone, Susan T., additional, Eleanor Inder, Terrie, additional, Ionasescu, Victor, additional, Jansen, Katrien, additional, Jiang, Yuwu, additional, Kaminski, Henry J., additional, Kamoshita, Shigehiko, additional, Kang, Peter B., additional, Kaufman, David M., additional, Kaufmann, Walter E., additional, Kaye, Edward M., additional, Kellaway, Peter, additional, Kelley, Rhona S., additional, Kennedy, Charles, additional, Kim, Young-Min, additional, Kirby, Michael, additional, Kirton, Adam, additional, Kobayashi, Eliane, additional, Kossoff, Eric H., additional, Koutroumanidis, Michail, additional, Krupp, Lauren, additional, Lange, Bernadette M., additional, Lanska, Douglas J., additional, Lanska, Mary Jo, additional, Larsen, Paul D., additional, Lassoff, Samuel J., additional, Laterra, John, additional, Lemieux, Bernard, additional, Lenn, Nicholas J., additional, Logan, William J., additional, Lomax, Elizabeth, additional, Longo, Lawrence D., additional, Lorris Betz, A., additional, Manyam, Bala V., additional, Marks, Warren A., additional, Massey, E. Wayne, additional, Mate, Laszlo J., additional, McKinlay, Ian, additional, McLean, William T., additional, McLellan, Ailsa, additional, Mehler, Mark F., additional, Melchior, Johannes C., additional, Michelson, David J., additional, Miller, Steven P., additional, Miller, Suzanne L., additional, Millichap, J. Gordon, additional, Minns, Robert A., additional, Mizrahi, Eli M., additional, Moser, Ann B., additional, Moshé, Solomon L., additional, Muhle, Hiltrud, additional, Muntoni, Francesco, additional, Naidu, Sakkubai, additional, Narayanan, Vinodh, additional, Nardocci, Nardo, additional, Neil, Jeffrey J., additional, Neumeyer, Ann, additional, Noetzel, Michael J., additional, Nomura, Yoshiko, additional, Nordli, Douglas R., additional, North, Kathryn, additional, Ohtsuka, Yoko, additional, O’Callaghan, Finbar J.K., additional, Packer, Roger J., additional, Pastores, Gregory M., additional, Patterson, Marc C., additional, Pearl, Phillip L., additional, Philippart, Michel, additional, Pihko, Helena S., additional, Piller, Gordon, additional, Platz, Thomas F., additional, Poduri, Annapurna, additional, Pollack, Michael A., additional, Porter, Brenda E., additional, Provis, Michèle, additional, Rating, Dietz, additional, Reich, Harold, additional, Remler, Bernd, additional, Rho, Jong M., additional, Richards, Peter, additional, Richardson, Edward P., additional, Richardson, Sylvia O., additional, Roach, E. Steve, additional, Rose, Arthur L., additional, Rozear, Marvin P., additional, Rubinstein, Lucien J., additional, Rust, Robert S., additional, Saini, Arushi Gahlot, additional, Saint-Anne Dargassies, Suzanne, additional, Sarnat, Harvey B., additional, Sarwar, Mohammad, additional, Satran, Richard, additional, Schneider, Sanford, additional, Schrank, Waltraud, additional, Scott, Rodney C., additional, Seinfeld, Syndi, additional, Selcen, Duygu, additional, Sestan, Nenad, additional, Shapiro, Steven, additional, Sherr, Elliott H., additional, Shevell, Michael, additional, Shield, Lloyd, additional, Sidman, Richard L., additional, Silverstein, Faye S., additional, Sinnreich, Michael, additional, Snead, O. Carter, additional, Solomons, Regan, additional, Soria-Duran, Emilio, additional, Stafstrom, Carl E., additional, Steven Roach, E., additional, Stevens, Harold, additional, Strassburg, Hans Michael, additional, Stumpf, David A., additional, Sullivan, Thomas, additional, Swick, Herbert M., additional, Swisher, Charles N., additional, Takahashi, Takao, additional, Tein, Ingrid, additional, Tochen, Laura, additional, Thomas, Eva E., additional, Thompson, Alan, additional, Toor, Svinder S., additional, Tyler, H. Richard, additional, Uldall, Peter, additional, Urion, David K., additional, Valappil, Ahsan Moosa Naduvil, additional, Van Toorn, Ronald, additional, Vermilion, Jennifer, additional, Vidaver, Doris, additional, Vohr, Betty R., additional, Vollmer, Brigitte, additional, Volpe, Joseph J., additional, Waber, Deborah P., additional, Wainwright, Mark S., additional, Waites, Lucius, additional, Walsh, Christopher, additional, Weindl, Adolf, additional, Whelan, Mary Anne, additional, White, Larry E., additional, Whittemore, Vicky Holets, additional, Wilmshurst, Jo, additional, Wirrell, Elaine, additional, Wolf, Nicole I., additional, Youssef, Paul, additional, Zempel, John, additional, Zoghbi, Huda Y., additional, Zuberi, Sameer M., additional, and Zupanc, Mary, additional

Published
2021
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6. Epileptic Syndromes in Infancy, Childhood and Adolescence Ed. 6

Author

Bureau, Michelle, Genton, Pierre, Dravet, Charlotte, Bureau, Michelle, Bureau, Michelle, Genton, Pierre, Dravet, Charlotte, and Bureau, Michelle

Abstract

Since 1984, the year of the publication of its first edition, the famous “Blue Guide” has been the international reference for paediatricians and neuropaediatricians with regard to epileptic syndromes in infants, children and adolescents. This 6th edition reviews some of the most noteworthy developments in the field, particularly in epileptic syndromes, but also focuses on the genetic aspects of the syndromes and their development. Progress brought about by advances in neuroimaging is also discussed in addition to specific etiologies such as parasitic diseases and immune and autoimmune diseases. The different backgrounds of the contributors - coordinators and authors – ensure that the book’s longstanding reputation for objectivity and seriousness, built over almost 35 years, remain well-deserved. This book written by the current leading specialists is recognized worldwide as the international reference in epilepsy.

Published
2019

11. EEG - The Epilepsies : EEG and epileptic syndromes Ed. 2

Author

Gélisse, Philippe, Crespel, Arielle, Bureau, Michelle, Gélisse, Philippe, Gélisse, Philippe, Crespel, Arielle, Bureau, Michelle, and Gélisse, Philippe

Abstract

Fully revised and updated, this second edition of the second volume of the Atlases of electroencephalography series includes more than 2/3 new high-quality digital figures. A new Classification approach to epileptic seizures and to the epilepsies became official in 2017. Several aspects in terms of terminology have been included in this book and most of the chapters have been rewritten. The second volume of this series on the practical use and interpretation of EEG focuses on epilepsies in their diversity. It is richly illustrated, and each EEG plate is analyzed in order to highlight the most significant elements to be used both for the diagnosis and interpretation. The originality of this textbook lies in its patient-based approach, thereby avoiding the pitfall of a formal presentation of EEG documents without their clinical context. Hence electroencephalography is placed at the core of the diagnostic and therapeutic discussion concerning patients with epilepsy. Given the practical orientation of this Atlas, the focus is on common forms of epilepsies; nevertheless, some less common, more intriguing forms have also been illustrated. A synthetic text summarizes the present approach to the main epilepsy categories. This Atlas is designed for all the actors who may be involved with patients with epilepsy. Physicians who deal with EEG will find it a valuable tool to improve the education of their early years, to help them with their interpretations later on, and for teaching purposes when more experienced. But it will also prove useful for all the physicians interested in epilepsy, as well as EEG technologists intent on providing quality recordings, and other professionals. Thorough understanding of human epilepsies requires extensive knowledge of their EEG correlates.

Published
2019

13. Síndromes epilépticos en lactantes, niños y adolescentes Ed. 5

Author

Bureau, Michelle, Genton, Pierre, Dravet, Charlotte, Bureau, Michelle, Bureau, Michelle, Genton, Pierre, Dravet, Charlotte, and Bureau, Michelle

Abstract

La herramienta de referencia para la epilepsia clínica y teórica. La epileptología se desarrolla. El enfoque sindrómico se complementa con un enfoque etiológico, basado sobre todo en los avances de la genética. Nuevas entidades han surgido, y un enfoque puramente electro-clínico no es ya suficiente en numerosas situaciones. Al igual que sus predecesores, la quinta edición de la Guía Azul incluye las recientes proyecciones que hicieron progresar nuestra comprensión de las epilepsias. Nos pareció necesario justificar los enfoques fisiológicos, epidemiológicos, genéticos y terapéuticos, y colocarlos en el contexto de los recientes esfuerzos de reclasificación de las epilepsias. A pesar de todo, la descripción de los síndromes epilépticos constituye siempre el corazón de esta obra. Un contenido ricamente ilustrado, con imagines de EEG, IRM, tablas comparativas,...

Published
2016

19. Consensus on diagnosis and management of JME: From founder's observations to current trends

Author

Kasteleijn- Nolst Trenité, Dorothée G.A., primary, Schmitz, Bettina, additional, Janz, Dieter, additional, Delgado-Escueta, Antonio V., additional, Thomas, Pierre, additional, Hirsch, Edouard, additional, Lerche, Holger, additional, Camfield, Carol, additional, Baykan, Betul, additional, Feucht, Martha, additional, Martínez-Juárez, Iris E., additional, Duron, Reyna M., additional, Medina, Marco T., additional, Rubboli, Guido, additional, Jerney, Judith, additional, Hermann, Bruce, additional, Yacubian, Elza, additional, Koutroumanidis, Michael, additional, Stephani, Ulrich, additional, Salas-Puig, Javier, additional, Reed, Ronald C., additional, Woermann, Friedrich, additional, Wandschneider, Britta, additional, Bureau, Michelle, additional, Gambardella, Antonio, additional, Koepp, Matthias J., additional, Gelisse, Philippe, additional, Gurses, Cardan, additional, Crespel, Arielle, additional, Nguyen-Michel, Vi Huong, additional, Ferlazzo, Edoardo, additional, Grisar, Thierry, additional, Helbig, Ingo, additional, Koeleman, Bobby P.C., additional, Striano, Pasquale, additional, Trimble, Michael, additional, Buono, Russel, additional, Cossette, Patrick, additional, Represa, Alfonso, additional, Dravet, Charlotte, additional, Serafini, Anna, additional, Berglund, Ivanka Savic-, additional, Sisodiya, Sanjay M., additional, Yamakawa, Kazuhiro, additional, and Genton, Pierre, additional

Published
2013
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21. Corrigendum to “Lennox–Gastaut syndrome in adulthood: Clinical and EEG features” [Epilepsy Res. 89 (2–3) (2010) 271–277]

Author

Ferlazzo, Edoardo, primary, Nikanorova, Marina, additional, Italiano, Domenico, additional, Bureau, Michelle, additional, Dravet, Charlotte, additional, Calarese, Tiziana, additional, Viallat, Danielle, additional, Kölmel, Margarethe, additional, Bramanti, Placido, additional, De Santi, Lorenzo, additional, and Genton, Pierre, additional

Published
2010
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25. Atlas d'électroencéphalographie - Volume 2

Author

Crespel Arielle, Gélisse Philippe, Bureau Michelle, Crespel Arielle, Gélisse Philippe, and Bureau Michelle

Subjects
Epilepsy, Electroencephalography, Electroencephalography--Atlases, Nervous system--Diseases--Atlases, Nervous system--Diseases
Abstract

Le deuxième tome de la série d'atlas d'électroencéphalographie est consacré aux épilepsies, qui sont abordées dans leur vaste diversité, selon les critères modernes de classification : épilepsies focales, épilepsies généralisées, encéphalopathies épileptiques, situations et étiologies particulières, crises réflexes. Comme dans le tome I, chaque planche d'EEG représentée est analysée pour en extraire les éléments significatifs, utiles au diagnostic et à l'interprétation. Les épilepsies les plus courantes sont privilégiées, en raison de l'orientation pratique de l'ouvrage, mais certaines formes moins communes, plus déroutantes, sont également illustrées. Un texte synthétique résume les conceptions actuelles des principales catégories d'épilepsies. Les médecins qui pratiquent l'EEG y trouveront une aide à l'interprétation. Cet ouvrage s'adresse également à tous les médecins qui prennent en charge les patients épileptiques, ainsi qu'aux techniciens des laboratoires de neurophysiologie.

Published
2006

32. Cortical myoclonus in angelman syndrome

Author

Guerrini, Renzo, primary, Bonanni, Paolo, additional, de Lorey, Timothy M., additional, Serratosa, Jos� M., additional, Moncla, Anne, additional, Malzac, Perrine, additional, Dravet, Charlotte, additional, Igvet, Marie Odile, additional, Bureau, Michelle, additional, Genton, Pierre, additional, Suisse, Georges, additional, Thomas, Pierre, additional, Sartucci, Ferdinando, additional, and Simi, Paolo, additional

Published
1996
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41. Les épilepsies myocloniques progressives : mythe ou réalité ?

Author

Genton, Pierre and Bureau, Michelle

Abstract

Les épilepsies myocloniques progressives (EMP) sont des maladies rares, et leur individualisation comme catégorie diagnostique et pronostique, bien qu'elle ait été reconnue par la dernière proposition de classification de la Ligue internationale contre l'épilepsie, peut sembler bien théorique à des cliniciens qui ont peu de chances d'en rencontrer dans leur pratique. Les EMP se définissent par l'association : 1) d'une épilepsie de type généralisé (bien que des crises focales soient possibles dans certaines étiologies), 2) d'un syndrome myoclonique souvent invalidant et 3) d'autres atteintes neurologiques (ataxie, démence, atteintes sensorielles), qui varient énormément en fonction de l'étiologie. Il s'agit en effet d'un groupe hétérogène de maladies répondant à des étiologies diverses. Leur prévalence varie en fonction du contexte ethnique et elles peuvent être relativement fréquentes sous certains climats, en raison de facteurs génétiques (isolat et/ou consanguinité, par exemple, pour les formes liées à une transmission récessive). Les anomalies génétiques et biochimiques responsables des EMP sont de mieux en mieux connues. Il faut, de nos jours, aborder le diagnostic des EMP de manière rationnelle, en tenant compte du contexte ethnique et génétique, de l'âge de survenue et du poids respectif des différents symptômes. Des outils thérapeutiques originaux sont en cours de développement et les traitements purement symptomatiques disponibles actuellement sont efficaces s'ils sont bien utilisés. Il est donc possible de reconnaître les EMP comme un groupe de maladies s'exprimant préférentiellement soit par une épilepsie, soit par un mouvement anormal, soit encore par des symptômes neurologiques ou cognitifs, et de prendre en charge ces affections rares de manière logique et globale. The progressive myoclonus epilepsies (PME) are rare diseases and many clinicians, who have only few opportunities to encounter such patients, may think of them as mythical. However, the category of PME has been retained by the latest classification scheme proposal of the International League Against Epilepsy. PMEs are defined by 1) generalized epileptic seizures (focal seizures may also occur in certain etiologies), 2) a sometimes invalidating myoclonus, and 3) other neurological symptoms (ataxia, dementia, sensory deficits) that vary according to etiology. Indeed, PMEs are a heterogenous group of conditions, with diverse etiologies. Their prevalence varies according to the ethnic context, and PMEs may appear as fairly frequent in some settings, because of genetic factors (isolate and/or inbreeding, for instance, in PMEs with recessive inheritance). The genetic and biochemical mechanisms underlying PMEs are increasingly recognized. We must nowadays follow a logical diagnostic scheme that will take into account the ethnic and genetic context, the age at onset of symptoms and the respective weight of symptoms. New therapeutic approaches are under development, and the available purely symptomatic treatments can be used to best possible effect. It is thus possible to recognize PMEs as a group of conditions appearing either as epilepsy, or as a movement disorder, or still under the mask of various neurological or cognitive symptoms. It is also possible to organize a logical, comprehensive care for patients with PME.

Published
2004
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43. Negative mycolonus.

Author

Guerrini, Renzo, Dravet, Charlotte, Genton, Pierre, Bureau, Michelle, Roger, Joseph, Rubboli, Guido, and Tassinari, Carlo Alberto

Published
1994
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45. Treatment of myoclonic epilepsies in infancy and early childhood.

Author

Sankar R, Wheless JW, Dravet C, Guerrini R, Medina MT, Bureau M, Genton P, and Delgado-Escueta AV

Subjects
Animals, Epilepsies, Myoclonic classification, Humans, Infant, Infant, Newborn, Spasms, Infantile drug therapy, Anticonvulsants therapeutic use, Epilepsies, Myoclonic drug therapy, Myoclonic Epilepsy, Juvenile drug therapy
Published
2005

46. Benign myoclonic epilepsy in infancy.

Author

Dravet C and Bureau M

Subjects
Age of Onset, Anticonvulsants therapeutic use, Child, Preschool, Epilepsies, Myoclonic drug therapy, Epilepsies, Myoclonic epidemiology, Female, Follow-Up Studies, Humans, Infant, Male, Mental Disorders physiopathology, Prognosis, Sex Distribution, Time Factors, Treatment Outcome, Valproic Acid therapeutic use, Electroencephalography methods, Epilepsies, Myoclonic classification, Epilepsies, Myoclonic physiopathology
Published
2005

47. Treatment of myoclonic epilepsies of childhood, adolescence, and adulthood.

Author

Medina MT, Martínez-Juárez IE, Durón RM, Genton P, Guerrini R, Dravet C, Bureau M, Perez-Gosiengfiao KT, Amador C, Bailey JN, Chaves-Sell F, and Delgado-Escueta AV

Subjects
Adolescent, Adult, Algorithms, Child, Child, Preschool, Drug Interactions, Drug Therapy, Combination, Epilepsies, Myoclonic classification, Epilepsies, Myoclonic complications, Female, Follow-Up Studies, Humans, Infant, Longitudinal Studies, Male, Myoclonic Epilepsy, Juvenile classification, Myoclonic Epilepsy, Juvenile etiology, Quality of Life, Review Literature as Topic, Risk Factors, Seizures drug therapy, Treatment Outcome, Anticonvulsants therapeutic use, Epilepsies, Myoclonic drug therapy, Myoclonic Epilepsy, Juvenile drug therapy
Published
2005

48. Severe myoclonic epilepsy in infancy: Dravet syndrome.

Author

Dravet C, Bureau M, Oguni H, Fukuyama Y, and Cokar O

Subjects
Age of Onset, Brain Mapping, Diagnosis, Differential, Electroencephalography classification, Epilepsies, Myoclonic epidemiology, Epilepsies, Myoclonic genetics, Epilepsies, Myoclonic therapy, Epilepsy, Absence physiopathology, Female, Functional Laterality physiology, Humans, Infant, Infant, Newborn, Male, Mortality, Psychomotor Performance physiology, Seizures classification, Seizures physiopathology, Syndrome, Treatment Outcome, Electroencephalography methods, Epilepsies, Myoclonic physiopathology
Published
2005

49. Myoclonic absences: the seizure and the syndrome.

Author

Bureau M and Tassinari CA

Subjects
Anticonvulsants therapeutic use, Autonomic Nervous System physiopathology, Child, Child, Preschool, Diagnosis, Differential, Electroencephalography methods, Electromyography methods, Epilepsies, Myoclonic diagnosis, Epilepsies, Myoclonic drug therapy, Female, Functional Laterality physiology, Humans, Male, Motor Activity physiology, Syndrome, Epilepsies, Myoclonic physiopathology, Seizures physiopathology
Published
2005

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