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Showing results (81-90 of 96) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|November 12, 2003
Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic interventionBrian P Zambrowicz, Alejandro Abuin, Ramiro Ramirez-Solis, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|June 13, 2021
Super-Refractory Status Epilepticus in Children: A Retrospective Cohort StudyAlejandra Vasquez, Raquel Farias-Moeller, Iván Sánchez-Fernández, et al.
Annals of Neurology|June 10, 2019
Autism and developmental disability caused by KCNQ3 gain-of-function variantsTristan T Sands, Francesco Miceli, Gaetan Lesca, et al.
Cold Spring Harbor Symposia on Quantitative Biology|September 2, 2004
High-throughput mouse knockouts provide a functional analysis of the genomeC J Friddle, A Abuin, R Ramirez-Solis, et al.
Neurology|July 3, 2020
Association of guideline publication and delays to treatment in pediatric status epilepticusIván Sánchez Fernández, Nicholas S Abend, Marta Amengual-Gual, et al.
Pediatric Neurology|May 22, 2021
Time to Treatment in Pediatric Convulsive Refractory Status Epilepticus: The Weekend EffectCristina Barcia Aguilar, Marta Amengual-Gual, Iván Sánchez Fernández, et al.
Nature Genetics|September 2, 2004
The knockout mouse projectChristopher P Austin, James F Battey, Allan Bradley, et al.
Epilepsia|July 12, 2021
Factors associated with long-term outcomes in pediatric refractory status epilepticusMarina Gaínza-Lein, Cristina Barcia Aguilar, Juan Piantino, et al.
Epilepsia|August 21, 2021
Benzodiazepine administration patterns before escalation to second-line medications in pediatric refractory convulsive status epilepticusTheodore Sheehan, Marta Amengual-Gual, Alejandra Vasquez, et al.
American Journal of Medical Genetics. Part A|September 9, 2018
Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literatureParisa Hemati, Anya Revah-Politi, Haim Bassan, et al.
Pageof 10

Showing results (81-90 of 96) with videos related to

Sort By:
Pageof 10
Proceedings of the National Academy of Sciences of the United States of America|November 12, 2003
Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic interventionBrian P Zambrowicz, Alejandro Abuin, Ramiro Ramirez-Solis, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|June 13, 2021
Super-Refractory Status Epilepticus in Children: A Retrospective Cohort StudyAlejandra Vasquez, Raquel Farias-Moeller, Iván Sánchez-Fernández, et al.
Annals of Neurology|June 10, 2019
Autism and developmental disability caused by KCNQ3 gain-of-function variantsTristan T Sands, Francesco Miceli, Gaetan Lesca, et al.
Cold Spring Harbor Symposia on Quantitative Biology|September 2, 2004
High-throughput mouse knockouts provide a functional analysis of the genomeC J Friddle, A Abuin, R Ramirez-Solis, et al.
Neurology|July 3, 2020
Association of guideline publication and delays to treatment in pediatric status epilepticusIván Sánchez Fernández, Nicholas S Abend, Marta Amengual-Gual, et al.
Pediatric Neurology|May 22, 2021
Time to Treatment in Pediatric Convulsive Refractory Status Epilepticus: The Weekend EffectCristina Barcia Aguilar, Marta Amengual-Gual, Iván Sánchez Fernández, et al.
Nature Genetics|September 2, 2004
The knockout mouse projectChristopher P Austin, James F Battey, Allan Bradley, et al.
Epilepsia|July 12, 2021
Factors associated with long-term outcomes in pediatric refractory status epilepticusMarina Gaínza-Lein, Cristina Barcia Aguilar, Juan Piantino, et al.
Epilepsia|August 21, 2021
Benzodiazepine administration patterns before escalation to second-line medications in pediatric refractory convulsive status epilepticusTheodore Sheehan, Marta Amengual-Gual, Alejandra Vasquez, et al.
American Journal of Medical Genetics. Part A|September 9, 2018
Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literatureParisa Hemati, Anya Revah-Politi, Haim Bassan, et al.
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