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Jacinta M Mcmahon

Showing results (1-10 of 38) with videos related to

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Developmental Medicine and Child Neurology|November 8, 2017
Sleep problems in Dravet syndrome: a modifiable comorbidityShane H Licheni, Jacinta M Mcmahon, Amy L Schneider, et al.
Archives of Neurology|March 14, 2012
Progressive gait deterioration in adolescents with Dravet syndromeJill M Rodda, Ingrid E Scheffer, Jacinta M McMahon, et al.
Epilepsia|December 22, 2017
ADGRV1 is implicated in myoclonic epilepsyKenneth A Myers, Steven Nasioulas, Amber Boys, et al.
Epilepsia|April 10, 2013
Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathiesSarah E Heron, Yeh Sze Ong, Simone C Yendle, et al.
Pediatrics|March 24, 2017
Fatal Cerebral Edema With Status Epilepticus in Children With Dravet Syndrome: Report of 5 CasesKenneth A Myers, Jacinta M McMahon, Simone A Mandelstam, et al.
The New England Journal of Medicine|October 1, 2010
Timing of de novo mutagenesis--a twin study of sodium-channel mutationsLata Vadlamudi, Leanne M Dibbens, Kate M Lawrence, et al.
Developmental Medicine and Child Neurology|April 28, 2015
Favourable response to ketogenic dietary therapies: undiagnosed glucose 1 transporter deficiency syndrome is only one factorNatasha E Schoeler, Judith Helen Cross, Suzanne Drury, et al.
Journal of Medical Genetics|July 11, 2009
De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal originSarah E Heron, Ingrid E Scheffer, Xenia Iona, et al.
Developmental Medicine and Child Neurology|December 17, 2013
Atypical multifocal Dravet syndrome lacks generalized seizures and may show later cognitive declineYoung Ok Kim, Susannah Bellows, Jacinta M McMahon, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 21, 2010
Detection of microchromosomal aberrations in refractory epilepsy: a pilot studyJacinta M McMahon, Ingrid E Scheffer, Jillian K Nicholl, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
Developmental Medicine and Child Neurology|November 8, 2017
Sleep problems in Dravet syndrome: a modifiable comorbidityShane H Licheni, Jacinta M Mcmahon, Amy L Schneider, et al.
Archives of Neurology|March 14, 2012
Progressive gait deterioration in adolescents with Dravet syndromeJill M Rodda, Ingrid E Scheffer, Jacinta M McMahon, et al.
Epilepsia|December 22, 2017
ADGRV1 is implicated in myoclonic epilepsyKenneth A Myers, Steven Nasioulas, Amber Boys, et al.
Epilepsia|April 10, 2013
Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathiesSarah E Heron, Yeh Sze Ong, Simone C Yendle, et al.
Pediatrics|March 24, 2017
Fatal Cerebral Edema With Status Epilepticus in Children With Dravet Syndrome: Report of 5 CasesKenneth A Myers, Jacinta M McMahon, Simone A Mandelstam, et al.
The New England Journal of Medicine|October 1, 2010
Timing of de novo mutagenesis--a twin study of sodium-channel mutationsLata Vadlamudi, Leanne M Dibbens, Kate M Lawrence, et al.
Developmental Medicine and Child Neurology|April 28, 2015
Favourable response to ketogenic dietary therapies: undiagnosed glucose 1 transporter deficiency syndrome is only one factorNatasha E Schoeler, Judith Helen Cross, Suzanne Drury, et al.
Journal of Medical Genetics|July 11, 2009
De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal originSarah E Heron, Ingrid E Scheffer, Xenia Iona, et al.
Developmental Medicine and Child Neurology|December 17, 2013
Atypical multifocal Dravet syndrome lacks generalized seizures and may show later cognitive declineYoung Ok Kim, Susannah Bellows, Jacinta M McMahon, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 21, 2010
Detection of microchromosomal aberrations in refractory epilepsy: a pilot studyJacinta M McMahon, Ingrid E Scheffer, Jillian K Nicholl, et al.
Pageof 4