Charlotte Dravet - bibliography

Bibliography

• C. Dravet:
  Les epilepsies graves de l’enfant. Vie Médicale 1978, 8: 543–548.
  
  
• C. Dravet, J. Roger, M. Bureau, B. Dalla Bernardina:
  Myoclonic epilepsies in childhood.
  In H. Aki-moto, H. Kazamatsuri, M. Seino, A. A. Ward Jr, editors: Advances in Epileptology, The XII-Ith Epilepsy International Symposium. New York, Raven Press 1982: 135–140
• P. Genton, M. T. Medina, J. Roger, C. Dravet et al.
  The spectrum of idiopathic generalized epilepsies: study of 230 prospectively clasified consecutive cases. Epilepsia, 1991, 32 (supplement 3): 45.
• C. Dravet, C. Julian, C. Legras, A. Magaudda, R, Guerrini, P. Genton, S. Soulayrol, N Giraud, E. Mesdjian, G. Trentin, et al.
  Epilepsy, antiepileptic drugs, and malformations in children of women with epilepsy: a French prospective cohort study.
  Neurology, Minneapolis, 1992, 42 (No. 4: Supplement 5): 75-82.
• P. Lerman:
  Benign partial epilepsy with centrotemporal spikes.
  In J. Roger, M. Bureau, C. Dravet, et al, editors: Epileptic syndromes in infancy, childhood and adolescence. 2nd edition pp. 189-200. London: John Libbey & Co. Ltd. 1992.
• J. Roger, P. Genton, M. Bureau, C. Dravet:
  Progressive myoclonus epilepsies in childhood and adolescence.
  In: J. Roger. M. Bureau, C. Dravet, F. E. Dreifuss, A. Perret , P. Wolf, editors: Epileptic syndromes in infancy: childhood and adolescence.
• J. Roger, M. Bureau, C. Dravet, Fritz Emanuel Dreifuss (1926-1997), A. Perret, P. Wolf, editors:
  Epileptic Syndromes in Infancy, Childhood and Adolescence.
  London: John Libbey, 1985. 2nd edition, 1992; 3rd edition 2002.
• P. Loiseau:
  Childhood absence epilepsy.
  In J. Roger, M. Bureau, C. Dravet, et al, editors: Epileptic syndromes in infancy, childhood and adolescence.
  2nd edition, 1992, London: John Libbey & Co. Ltd. Pp. 135-150.
• J. Roger, P. Genton, M. Bureau, M. T. Medina, C. Dravet:
  La nueva clasificación de las epilepsias y de los síndromes epilépticos adoptan en nueva Delhi en 1989. Revista ecuatoriana de neurologia, 1992, 1: 3-13.
• C. Dravet, R. Guerrini, J. Mancini, A. Saltarelli, M. O. Livet, and M. C. Galland:
  Different outcomes of epilepsy due to cortical dysplastic lesions.
  In R. Guerrini, editor: Dysplasias of Cerebral Cortex and Epilepsy. Philadelphia: Lippincott-Raven Publishers, 1996.
• R. Guerrini, T. M. DeLorey, P. Bonanni, A. Moncla, C. Dravet, G. Suise, Suisse, M. O. Livet, M. Bureau, P. Malzac, P. Genton, P. Thomas, F. Sartucci, P. Simi, and J. M. Serratosa:
  Cortical myoclonus of Angelman syndrome.
  Annals of Neurology, Boston, 1996, 40: 39-48.
• Pierre Labauge, Réda Ouazzani, Amel Mrabet, Djamel Grid, Pierre Genton, Charlotte Dravet, Taieb Chkili, Corrine Beck, Catherine Buresi, Michel Baldy Moulinier, Alain Malafosse:
  Allelic Heterogeneity of Mediterranean Myoclonus and the Cystatin B Gene.
  Annals of Neurology, Boston, 1997, 41 : 686-689.
• P. Wolf
  Epilepsy with grand mal on awakening.
  In J. Roger, M. Bureau, C. Dravet, et al. (Eds.), Epileptic syndromes in infancy, childhood and adolescence. London: John Libbey & Co.Ltd. 2nd edition, 1997, pp. 329-342.
• J. M. Serratosa, P. Gomez-Garre, M. E. Gallardo, B. Anta, D. Beltran-Valero deBernabe, D. Lindhout, P. B. Augustijn, C. A. Tassinari, R. Michelucci, R. M. A. Malafosse, M. Topcu, D. Grid, C. Dravet, S. F. Berkovic, S. Rodriguez de Cordoba:
  A novel proteintyrosine phosphatase gene is mutated in progressive myoclonusepilepsy of the Lafora type (EPM2).
  Human Molecular Genetics, Oxford, 1999, 8: 345-352.
• C. Dravet, M. Bureau, H. Oguni, Y. Fukuyama, O. Cokar:
  Severe myoclonic epilepsy in infancy (Dravet syndrome).
  In J. Roger, M. Bureau, Ch. Dravet, P. Genton, C. A. Tassinari, P. Wolf, editors: Epileptic Syndromes in Infancy, Childhood and Adolescence. 3rd edition. Eastleigh, John Libbey & Co Ltd 2002: 81–103.