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Anna Rylova

Showing results (1-10 of 6) with videos related to

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Journal of Neurosurgical Anesthesiology|February 23, 2018
Protecting the Brain With Xenon Anesthesia for Neurosurgical ProceduresAnna Rylova, Mervyn Maze
Journal of Neurosurgical Anesthesiology|February 28, 2012
Awake craniotomy under xenon anesthesia: first experienceAlexander Kulikov, Anna Rylova, Andrey Lubnin
Journal of Molecular Neuroscience : MN|May 21, 2011
Comparative analysis of the behavioral and biomolecular parameters of four mouse strainsElimelech Nesher, Vladimir Peskov, Anna Rylova, et al.
Journal of Anaesthesiology, Clinical Pharmacology|November 11, 2021
Intravenous lidocaine infusion in a case of severe COVID-19 infectionAnna Rylova, Seema Chowdhury, Houman Amirfarzan, et al.
Immunological Investigations|January 29, 2019
Neutrophil Functions in Immunodeficiency Due to DOCK8 DeficiencyAmarilla B Mandola, Jacov Levy, Amit Nahum, et al.
The Journal of Experimental Medicine|July 20, 2016
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defectsAmos J Simon, Atar Lev, Yong Zhang, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Journal of Neurosurgical Anesthesiology|February 23, 2018
Protecting the Brain With Xenon Anesthesia for Neurosurgical ProceduresAnna Rylova, Mervyn Maze
Journal of Neurosurgical Anesthesiology|February 28, 2012
Awake craniotomy under xenon anesthesia: first experienceAlexander Kulikov, Anna Rylova, Andrey Lubnin
Journal of Molecular Neuroscience : MN|May 21, 2011
Comparative analysis of the behavioral and biomolecular parameters of four mouse strainsElimelech Nesher, Vladimir Peskov, Anna Rylova, et al.
Journal of Anaesthesiology, Clinical Pharmacology|November 11, 2021
Intravenous lidocaine infusion in a case of severe COVID-19 infectionAnna Rylova, Seema Chowdhury, Houman Amirfarzan, et al.
Immunological Investigations|January 29, 2019
Neutrophil Functions in Immunodeficiency Due to DOCK8 DeficiencyAmarilla B Mandola, Jacov Levy, Amit Nahum, et al.
The Journal of Experimental Medicine|July 20, 2016
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defectsAmos J Simon, Atar Lev, Yong Zhang, et al.
Pageof 1