MARC Record from harvard_bibliographic_metadata

LEADER: 03566pam a22003374a 4500
001 010732375-3
005 20070810110427.0
008 070731s2005 pauac b 001 0 eng
010 $a 2004016011
020 $a9780781752480 (hardcover)
020 $a0781752485 (hardcover)
035 0 $aocm56823490
040 $aDNLM$cDNLM
041 0 $aeng
042 $apcc
060 00 $aW1$bAD684H v.95 2005
060 10 $aWL 385$bM9955 2005
245 00 $aMyoclonic epilepsies /$ceditors, Antonio V. Delgado-Escueta ... [et al.].
260 $aPhiladelphia :$bLippincott Williams & Wilkins,$c2005.
300 $axxiii, 331 p. :$bill., ports. ;$c27 cm.
440 0 $aAdvances in neurology,$x0091-3952 ;$vv. 95
504 $aIncludes bibliographical references and index.
505 0 $aHistory and classification of "myoclonic" epilepsies: from seizures to syndromes to diseases / Pierre Genton ... [et al.] -- Ontogeny of the reticular formation: its possible relation to the myoclonic epilepsies / Harvey B. Sarnat -- Pathophysiology of myoclonic epilepsies / Renzo Guerrini ... [et al.] -- Progressive myoclonus epilepsies: EPM1, EPM2A, EPM2B / Elayne M. Chan -- Myoclonic status in non-progressive encephalopathies / Bernardo Dalla Bernardina -- Severe myoclonic epilepsy in infancy: Dravet syndrome / Charlotte Dravet ... [et al.].
505 8 $aSevere myoclonic epilepsy in infancy: clinical analysis and relation to SCN1A mutations in a Japanese cohort / Hirokazu Oguni ... [et al.] -- Myoclonic seizures in the context of generalized epilepsy with febrile seizures plus (GEFS+) / Michel Baulac ... [et al.] -- Benign myoclonic epilepsy in infancy / Charlotte Dravet and Michelle Bureau -- Autosomal recessive benign myoclonic epilepsy of infancy / Federico Zara and Fabrizio A. De Falco -- Myoclonic-astatic epilepsy of early childhood-definition, course, nosography, genetics / B.A. Neubauer ... [et al.].
505 8 $aIdiopathic myoclonic-astatic epilepsy of early childhood-nosology based on electrophysiological and long-term follow-up study of patients / Hirokazu Oguni ... [et al.] -- Myoclonic absences: the seizure and the syndrome / Michelle Bureau and Carlo Alberto Tassinari -- Eyelid myoclonia and absence / Athanasios Covanis -- Childhood absence epilepsy evolving to juvenile myoclonic epilepsy: electroclinical and genetic features / Marco T. Medina ... [et al.] -- Photosensitivity: genetics and clinical significance / B.A. Neubauer ... [et al.] -- Familial juvenile myoclonic epilepsy / Maria Elisa Alonso ... [et al.].
505 8 $aGenetics of juvenile myoclonic epilepsy: faulty components and faulty wiring? / Martina Durner, Deb Pal, and David Greenberg -- Autosomal dominant juvenile myoclonic epilepsy and GABRA1 / Patrick Cossette ... [et al.] -- CLCN2 and idiopathic generalized epilepsy / Armin Heils -- Autosomal dominant cortical myoclonus and epilepsy (ADCME) with linkage to chromosome 2p11.1-Q12.2 / Renzo Guerrini ... [et al.] -- Familial adult myoclonic epilepsy (FAME) / Eiichiro Uyama, Ying-Hui Fu, and Louis J. Ptácek -- Treatment of myoclonic epilepsies in infancy and early childhood / Raman Sankar ... [et al.].
505 8 $aKetogenic diet in patients with Dravet syndrome and myoclonic epilepsies in infancy and early childhood / Natalio Fejerman, Roberto Caraballo, and Ricardo Cersosimo -- Treatment of myoclonic epilepsies of childhood, adolescence, and adulthood / Marco T. Medina ... [et al.].
650 12 $aEpilepsies, Myoclonic.
700 1 $aDelgado-Escueta, Antonio V.
988 $a20070731
906 $0OCLC