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Alexandre N Datta

Showing results (41-50 of 57) with videos related to

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Communications Medicine|May 23, 2022
Personalised therapeutic management of epileptic patients guided by pathway-driven breath metabolomicsKapil Dev Singh, Martin Osswald, Victoria C Ziesenitz, et al.
Journal of Sleep Research|June 10, 2024
Hyperarousal features in the sleep architecture of individuals with and without insomniaTobias Di Marco, Thomas E Scammell, Kolia Sadeghi, et al.
Annals of Neurology|April 22, 2018
Feasibility, safety, and outcome of recanalization treatment in childhood strokeSandra Bigi, Andrea Dulcey, Jan Gralla, et al.
Molecular Genetics and Metabolism Reports|February 3, 2021
Co-therapy with S-adenosylmethionine and nicotinamide riboside improves t-cell survival and function in Arts Syndrome (PRPS1 deficiency)Nina Lenherr, John Christodoulou, John Duley, et al.
Pediatrics|April 22, 2015
Incidence and outcomes of symptomatic neonatal arterial ischemic strokeSebastian Grunt, Lea Mazenauer, Sarah E Buerki, et al.
Sleep|April 22, 2024
Effect of daridorexant on sleep architecture in patients with chronic insomnia disorder: a pooled post hoc analysis of two randomized phase 3 clinical studiesTobias Di Marco, Ina Djonlagic, Yves Dauvilliers, et al.
Stroke|August 20, 2020
Risk Factors for Postprocedural Arterial Ischemic Stroke in Children With Cardiac DiseaseBettina C Henzi, Barbara Brotschi, Christian Balmer, et al.
Epilepsy Research|October 21, 2022
EEG parameters as endpoints in epilepsy clinical trials - An expert panel opinion paperJeffrey Buchhalter, Caroline Neuray, Jocelyn Y Cheng, et al.
Human Molecular Genetics|January 2, 2015
MTO1 mediates tissue specificity of OXPHOS defects via tRNA modification and translation optimization, which can be bypassed by dietary interventionChristin Tischner, Annette Hofer, Veronika Wulff, et al.
Brain : a Journal of Neurology|November 20, 2016
De novo GABRG2 mutations associated with epileptic encephalopathiesDingding Shen, Ciria C Hernandez, Wangzhen Shen, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Communications Medicine|May 23, 2022
Personalised therapeutic management of epileptic patients guided by pathway-driven breath metabolomicsKapil Dev Singh, Martin Osswald, Victoria C Ziesenitz, et al.
Journal of Sleep Research|June 10, 2024
Hyperarousal features in the sleep architecture of individuals with and without insomniaTobias Di Marco, Thomas E Scammell, Kolia Sadeghi, et al.
Annals of Neurology|April 22, 2018
Feasibility, safety, and outcome of recanalization treatment in childhood strokeSandra Bigi, Andrea Dulcey, Jan Gralla, et al.
Molecular Genetics and Metabolism Reports|February 3, 2021
Co-therapy with S-adenosylmethionine and nicotinamide riboside improves t-cell survival and function in Arts Syndrome (PRPS1 deficiency)Nina Lenherr, John Christodoulou, John Duley, et al.
Pediatrics|April 22, 2015
Incidence and outcomes of symptomatic neonatal arterial ischemic strokeSebastian Grunt, Lea Mazenauer, Sarah E Buerki, et al.
Sleep|April 22, 2024
Effect of daridorexant on sleep architecture in patients with chronic insomnia disorder: a pooled post hoc analysis of two randomized phase 3 clinical studiesTobias Di Marco, Ina Djonlagic, Yves Dauvilliers, et al.
Stroke|August 20, 2020
Risk Factors for Postprocedural Arterial Ischemic Stroke in Children With Cardiac DiseaseBettina C Henzi, Barbara Brotschi, Christian Balmer, et al.
Epilepsy Research|October 21, 2022
EEG parameters as endpoints in epilepsy clinical trials - An expert panel opinion paperJeffrey Buchhalter, Caroline Neuray, Jocelyn Y Cheng, et al.
Human Molecular Genetics|January 2, 2015
MTO1 mediates tissue specificity of OXPHOS defects via tRNA modification and translation optimization, which can be bypassed by dietary interventionChristin Tischner, Annette Hofer, Veronika Wulff, et al.
Brain : a Journal of Neurology|November 20, 2016
De novo GABRG2 mutations associated with epileptic encephalopathiesDingding Shen, Ciria C Hernandez, Wangzhen Shen, et al.
Pageof 6