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Renzo Guerrini

Showing results (391-400 of 611) with videos related to

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Cerebral Cortex (New York, N.Y. : 1991)|July 10, 2023
CDKL5 deficiency disorder: progressive brain atrophy may be part of the syndromeNicola Specchio, Marina Trivisano, Matteo Lenge, et al.
Scientific Reports|November 29, 2019
Pre-diagnosing and managing patients with GM1 gangliosidosis and related disorders by the evaluation of GM1 ganglioside contentRodolfo Tonin, Anna Caciotti, Elena Procopio, et al.
Epilepsia|August 6, 2023
Fenfluramine in the treatment of Dravet syndrome: Results of a third randomized, placebo-controlled clinical trialJoseph Sullivan, Lieven Lagae, J Helen Cross, et al.
Annals of Neurology|July 3, 2003
Nonsyndromic mental retardation and cryptogenic epilepsy in women with doublecortin gene mutationsRenzo Guerrini, Francesca Moro, Eva Andermann, et al.
Epilepsy & Behavior : E&B|February 20, 2019
Outcome after hemispherotomy in patients with intractable epilepsy: Comparison of techniques in the Italian experienceLuca de Palma, Nicola Pietrafusa, Francesca Gozzo, et al.
Lancet (London, England)|December 22, 2019
Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trialLieven Lagae, Joseph Sullivan, Kelly Knupp, et al.
European Journal of Human Genetics : EJHG|February 22, 2018
Clinical and genetic spectrum of AMPD2-related pontocerebellar hypoplasia type 9Fanny Kortüm, Rami Abou Jamra, Malik Alawi, et al.
Epilepsia|January 6, 2011
A duplication in 1q21.3 in a family with early onset and childhood absence epilepsyHiltrud Muhle, Ines Steinich, Sarah von Spiczak, et al.
Cell Reports|December 6, 2018
A Primate-Specific Isoform of PLEKHG6 Regulates Neurogenesis and Neuronal MigrationAdam C O'Neill, Christina Kyrousi, Johannes Klaus, et al.
Neurology|March 7, 2014
Role of the phosphoinositide phosphatase FIG4 gene in familial epilepsy with polymicrogyriaStéphanie Baulac, Guy M Lenk, Béatrice Dufresnois, et al.
Pageof 62

Showing results (391-400 of 611) with videos related to

Sort By:
Pageof 62
Cerebral Cortex (New York, N.Y. : 1991)|July 10, 2023
CDKL5 deficiency disorder: progressive brain atrophy may be part of the syndromeNicola Specchio, Marina Trivisano, Matteo Lenge, et al.
Scientific Reports|November 29, 2019
Pre-diagnosing and managing patients with GM1 gangliosidosis and related disorders by the evaluation of GM1 ganglioside contentRodolfo Tonin, Anna Caciotti, Elena Procopio, et al.
Epilepsia|August 6, 2023
Fenfluramine in the treatment of Dravet syndrome: Results of a third randomized, placebo-controlled clinical trialJoseph Sullivan, Lieven Lagae, J Helen Cross, et al.
Annals of Neurology|July 3, 2003
Nonsyndromic mental retardation and cryptogenic epilepsy in women with doublecortin gene mutationsRenzo Guerrini, Francesca Moro, Eva Andermann, et al.
Epilepsy & Behavior : E&B|February 20, 2019
Outcome after hemispherotomy in patients with intractable epilepsy: Comparison of techniques in the Italian experienceLuca de Palma, Nicola Pietrafusa, Francesca Gozzo, et al.
Lancet (London, England)|December 22, 2019
Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trialLieven Lagae, Joseph Sullivan, Kelly Knupp, et al.
European Journal of Human Genetics : EJHG|February 22, 2018
Clinical and genetic spectrum of AMPD2-related pontocerebellar hypoplasia type 9Fanny Kortüm, Rami Abou Jamra, Malik Alawi, et al.
Epilepsia|January 6, 2011
A duplication in 1q21.3 in a family with early onset and childhood absence epilepsyHiltrud Muhle, Ines Steinich, Sarah von Spiczak, et al.
Cell Reports|December 6, 2018
A Primate-Specific Isoform of PLEKHG6 Regulates Neurogenesis and Neuronal MigrationAdam C O'Neill, Christina Kyrousi, Johannes Klaus, et al.
Neurology|March 7, 2014
Role of the phosphoinositide phosphatase FIG4 gene in familial epilepsy with polymicrogyriaStéphanie Baulac, Guy M Lenk, Béatrice Dufresnois, et al.
Pageof 62