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Renzo Guerrini

Showing results (221-230 of 611) with videos related to

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Drugs|November 18, 2019
Drug Development for Rare Paediatric Epilepsies: Current State and Future DirectionsStéphane Auvin, Andreja Avbersek, Thomas Bast, et al.
Developmental Medicine and Child Neurology|September 8, 2015
The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathyElena Cellini, Aglaia Vignoli, Tiziana Pisano, et al.
Life Sciences|November 24, 2020
Thermal inactivation of SARS COVID-2 virus: Are steam inhalations a potential treatment?Giancarlo la Marca, Jacopo Barp, Stefano Frenos, et al.
Epilepsia|November 15, 2021
Distinct epilepsy phenotypes and response to drugs in KCNA1 gain- and loss-of function variantsFrancesco Miceli, Renzo Guerrini, Mario Nappi, et al.
Epilepsia|June 19, 2019
Advancing research toward faster diagnosis, better treatment, and end of stigma in epilepsyAsla Pitkänen, David C Henshall, J Helen Cross, et al.
Epilepsia|April 6, 2023
Genetics of familial adult myoclonus epilepsy: From linkage studies to noncoding repeat expansionsMark A Corbett, Christel Depienne, Liana Veneziano, et al.
Annals of Clinical and Translational Neurology|January 13, 2017
Unilobar surgery for symptomatic epileptic spasmsCarmen Barba, Roberto Mai, Laura Grisotto, et al.
American Journal of Medical Genetics. Part A|June 9, 2012
Periventricular heterotopia with white matter abnormalities associated with 6p25 deletionElena Cellini, Vittoria Disciglio, Francesca Novara, et al.
Developmental Medicine and Child Neurology|March 5, 2019
Perception of impact of Dravet syndrome on children and caregivers in multiple countries: looking beyond seizuresRima Nabbout, Stephane Auvin, Catherine Chiron, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 22, 2015
Biotinidase deficiency due to a de novo mutation or gonadal mosaicism in a first childRodolfo Tonin, Anna Caciotti, Silvia Funghini, et al.
Pageof 62

Showing results (221-230 of 611) with videos related to

Sort By:
Pageof 62
Drugs|November 18, 2019
Drug Development for Rare Paediatric Epilepsies: Current State and Future DirectionsStéphane Auvin, Andreja Avbersek, Thomas Bast, et al.
Developmental Medicine and Child Neurology|September 8, 2015
The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathyElena Cellini, Aglaia Vignoli, Tiziana Pisano, et al.
Life Sciences|November 24, 2020
Thermal inactivation of SARS COVID-2 virus: Are steam inhalations a potential treatment?Giancarlo la Marca, Jacopo Barp, Stefano Frenos, et al.
Epilepsia|November 15, 2021
Distinct epilepsy phenotypes and response to drugs in KCNA1 gain- and loss-of function variantsFrancesco Miceli, Renzo Guerrini, Mario Nappi, et al.
Epilepsia|June 19, 2019
Advancing research toward faster diagnosis, better treatment, and end of stigma in epilepsyAsla Pitkänen, David C Henshall, J Helen Cross, et al.
Epilepsia|April 6, 2023
Genetics of familial adult myoclonus epilepsy: From linkage studies to noncoding repeat expansionsMark A Corbett, Christel Depienne, Liana Veneziano, et al.
Annals of Clinical and Translational Neurology|January 13, 2017
Unilobar surgery for symptomatic epileptic spasmsCarmen Barba, Roberto Mai, Laura Grisotto, et al.
American Journal of Medical Genetics. Part A|June 9, 2012
Periventricular heterotopia with white matter abnormalities associated with 6p25 deletionElena Cellini, Vittoria Disciglio, Francesca Novara, et al.
Developmental Medicine and Child Neurology|March 5, 2019
Perception of impact of Dravet syndrome on children and caregivers in multiple countries: looking beyond seizuresRima Nabbout, Stephane Auvin, Catherine Chiron, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 22, 2015
Biotinidase deficiency due to a de novo mutation or gonadal mosaicism in a first childRodolfo Tonin, Anna Caciotti, Silvia Funghini, et al.
Pageof 62