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Michael F Waters

Showing results (51-60 of 64) with videos related to

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JAMA Neurology|January 10, 2016
Factors Associated With Recurrent Ischemic Stroke in the Medical Group of the SAMMPRIS TrialMichael F Waters, Brian L Hoh, Michael J Lynn, et al.
Neurobiology of Disease|August 26, 2014
KCNC3(R420H), a K(+) channel mutation causative in spinocerebellar ataxia 13 displays aberrant intracellular traffickingCarolina Gallego-Iradi, Justin S Bickford, Swati Khare, et al.
Stroke|December 25, 2018
Hemodynamic Markers in the Anterior Circulation as Predictors of Recurrent Stroke in Patients With Intracranial StenosisAshley M Wabnitz, Colin P Derdeyn, David J Fiorella, et al.
Nature Genetics|February 28, 2006
Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypesMichael F Waters, Natali A Minassian, Giovanni Stevanin, et al.
Annals of Neurology|October 9, 2018
Fingolimod enhances the efficacy of delayed alteplase administration in acute ischemic stroke by promoting anterograde reperfusion and retrograde collateral flowDe-Cai Tian, Kaibin Shi, Zilong Zhu, et al.
Science Advances|June 12, 2020
Neutrophil extracellular traps exacerbate neurological deficits after traumatic brain injuryKumar Vaibhav, Molly Braun, Katelyn Alverson, et al.
Cell|March 22, 2016
Kv3.3 Channels Bind Hax-1 and Arp2/3 to Assemble a Stable Local Actin Network that Regulates Channel GatingYalan Zhang, Xiao-Feng Zhang, Matthew R Fleming, et al.
Journal of the American Heart Association|February 16, 2017
Racial-Ethnic Disparities in Acute Stroke Care in the Florida-Puerto Rico Collaboration to Reduce Stroke Disparities StudyRalph L Sacco, Hannah Gardener, Kefeng Wang, et al.
Journal of Neurosurgery|November 21, 2015
CYP2C19 and CES1 polymorphisms and efficacy of clopidogrel and aspirin dual antiplatelet therapy in patients with symptomatic intracranial atherosclerotic diseaseBrian L Hoh, Yan Gong, Caitrin W McDonough, et al.
Plos One|May 4, 2017
A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR traffickingSwati Khare, Jerelyn A Nick, Yalan Zhang, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
JAMA Neurology|January 10, 2016
Factors Associated With Recurrent Ischemic Stroke in the Medical Group of the SAMMPRIS TrialMichael F Waters, Brian L Hoh, Michael J Lynn, et al.
Neurobiology of Disease|August 26, 2014
KCNC3(R420H), a K(+) channel mutation causative in spinocerebellar ataxia 13 displays aberrant intracellular traffickingCarolina Gallego-Iradi, Justin S Bickford, Swati Khare, et al.
Stroke|December 25, 2018
Hemodynamic Markers in the Anterior Circulation as Predictors of Recurrent Stroke in Patients With Intracranial StenosisAshley M Wabnitz, Colin P Derdeyn, David J Fiorella, et al.
Nature Genetics|February 28, 2006
Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypesMichael F Waters, Natali A Minassian, Giovanni Stevanin, et al.
Annals of Neurology|October 9, 2018
Fingolimod enhances the efficacy of delayed alteplase administration in acute ischemic stroke by promoting anterograde reperfusion and retrograde collateral flowDe-Cai Tian, Kaibin Shi, Zilong Zhu, et al.
Science Advances|June 12, 2020
Neutrophil extracellular traps exacerbate neurological deficits after traumatic brain injuryKumar Vaibhav, Molly Braun, Katelyn Alverson, et al.
Cell|March 22, 2016
Kv3.3 Channels Bind Hax-1 and Arp2/3 to Assemble a Stable Local Actin Network that Regulates Channel GatingYalan Zhang, Xiao-Feng Zhang, Matthew R Fleming, et al.
Journal of the American Heart Association|February 16, 2017
Racial-Ethnic Disparities in Acute Stroke Care in the Florida-Puerto Rico Collaboration to Reduce Stroke Disparities StudyRalph L Sacco, Hannah Gardener, Kefeng Wang, et al.
Journal of Neurosurgery|November 21, 2015
CYP2C19 and CES1 polymorphisms and efficacy of clopidogrel and aspirin dual antiplatelet therapy in patients with symptomatic intracranial atherosclerotic diseaseBrian L Hoh, Yan Gong, Caitrin W McDonough, et al.
Plos One|May 4, 2017
A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR traffickingSwati Khare, Jerelyn A Nick, Yalan Zhang, et al.
Pageof 7