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Alfred L George

Showing results (141-150 of 296) with videos related to

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Neurobiology of Disease|March 24, 2018
Direct evidence of impaired neuronal Na/K-ATPase pump function in alternating hemiplegia of childhoodChristine Q Simmons, Christopher H Thompson, Bryan E Cawthon, et al.
Biorxiv : the Preprint Server for Biology|March 3, 2023
Epilepsy-associated <i>SCN2A</i> (Na <sub>V</sub> 1.2) Variants Exhibit Diverse and Complex Functional PropertiesChristopher H Thompson, Franck Potet, Tatiana V Abramova, et al.
Neurobiology of Disease|April 30, 2020
Neuronal modeling of alternating hemiplegia of childhood reveals transcriptional compensation and replicates a trigger-induced phenotypeJohn P Snow, Grant Westlake, Lindsay K Klofas, et al.
Experimental Neurology|August 13, 2013
Functional characterization of ClC-1 mutations from patients affected by recessive myotonia congenita presenting with different clinical phenotypesJean-François Desaphy, Gianluca Gramegna, Concetta Altamura, et al.
Journal of Hypertension|February 21, 2009
CLCNKB-T481S and essential hypertension in a Ghanaian populationSaba Sile, Digna R Velez, Niloufar B Gillani, et al.
International Journal of Cardiology|September 18, 2012
Novel deletion mutation in the cardiac sodium channel inactivation gate causes long QT syndromeNicola Detta, Giulia Frisso, Alberto Zullo, et al.
Heart Rhythm|April 27, 2005
Polymorphic ventricular tachycardia and KCNJ2 mutationsTerrence U H Chun, Michael R Epstein, Macdonald Dick, et al.
International Journal of Molecular Sciences|July 28, 2017
Allelic Complexity in Long QT Syndrome: A Family-Case StudyAlberto Zullo, Giulia Frisso, Nicola Detta, et al.
Journal of Clinical Psychopharmacology|February 29, 2024
Concentrations of Fluoxetine Enantiomers Decline During Pregnancy and Increase After BirthKatherine L Wisner, Michael J Avram, Alfred L George, et al.
The Journal of Clinical Investigation|October 3, 2003
Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)D Woodrow Benson, Dao W Wang, Macaira Dyment, et al.
Pageof 30

Showing results (141-150 of 296) with videos related to

Sort By:
Pageof 30
Neurobiology of Disease|March 24, 2018
Direct evidence of impaired neuronal Na/K-ATPase pump function in alternating hemiplegia of childhoodChristine Q Simmons, Christopher H Thompson, Bryan E Cawthon, et al.
Biorxiv : the Preprint Server for Biology|March 3, 2023
Epilepsy-associated <i>SCN2A</i> (Na <sub>V</sub> 1.2) Variants Exhibit Diverse and Complex Functional PropertiesChristopher H Thompson, Franck Potet, Tatiana V Abramova, et al.
Neurobiology of Disease|April 30, 2020
Neuronal modeling of alternating hemiplegia of childhood reveals transcriptional compensation and replicates a trigger-induced phenotypeJohn P Snow, Grant Westlake, Lindsay K Klofas, et al.
Experimental Neurology|August 13, 2013
Functional characterization of ClC-1 mutations from patients affected by recessive myotonia congenita presenting with different clinical phenotypesJean-François Desaphy, Gianluca Gramegna, Concetta Altamura, et al.
Journal of Hypertension|February 21, 2009
CLCNKB-T481S and essential hypertension in a Ghanaian populationSaba Sile, Digna R Velez, Niloufar B Gillani, et al.
International Journal of Cardiology|September 18, 2012
Novel deletion mutation in the cardiac sodium channel inactivation gate causes long QT syndromeNicola Detta, Giulia Frisso, Alberto Zullo, et al.
Heart Rhythm|April 27, 2005
Polymorphic ventricular tachycardia and KCNJ2 mutationsTerrence U H Chun, Michael R Epstein, Macdonald Dick, et al.
International Journal of Molecular Sciences|July 28, 2017
Allelic Complexity in Long QT Syndrome: A Family-Case StudyAlberto Zullo, Giulia Frisso, Nicola Detta, et al.
Journal of Clinical Psychopharmacology|February 29, 2024
Concentrations of Fluoxetine Enantiomers Decline During Pregnancy and Increase After BirthKatherine L Wisner, Michael J Avram, Alfred L George, et al.
The Journal of Clinical Investigation|October 3, 2003
Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)D Woodrow Benson, Dao W Wang, Macaira Dyment, et al.
Pageof 30