Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

John J Alexander

Showing results (1-10 of 35) with videos related to

Pageof 4
Sort By:
Advances in Experimental Medicine and Biology|January 15, 2008
Adeno-associated viral vectors and the retinaJohn J Alexander, William W Hauswirth
Drug News & Perspectives|July 4, 2008
Prospects for retinal cone-targeted gene therapyJohn J Alexander, William W Hauswirth
Journal of Child Neurology|September 15, 2006
Stroke associated with central nervous system vasculitis after West Nile virus infectionJohn J Alexander, Andrew S Lasky, William D Graf
American Journal of Medical Genetics. Part A|July 29, 2018
Is exon 8 the most critical or the only dispensable exon of the VCAN gene? Insights into VCAN variants and clinical spectrum of Wagner syndromeArunkanth Ankala, Nieraj Jain, Baker Hubbard, et al.
Pediatric Neurology|October 24, 2017
Diagnostic Yield From 339 Epilepsy Patients Screened on a Clinical Gene PanelKameryn M Butler, Cristina da Silva, John J Alexander, et al.
Pediatrics|October 8, 2008
Neuroimaging-use trends in nonacute pediatric headache before and after clinical practice parametersWilliam D Graf, Husam R Kayyali, John J Alexander, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 21, 2019
SubILM Injection of AAV for Gene Delivery to the RetinaPaul D Gamlin, John J Alexander, Sanford L Boye, et al.
Case Reports in Genetics|November 10, 2018
Epileptic Encephalopathy and Cerebellar Atrophy Resulting from Compound Heterozygous <i>CACNA2D2</i> VariantsKameryn M Butler, Philip J Holt, Sarah S Milla, et al.
Brain : a Journal of Neurology|July 3, 2018
De novo variants in GABRA2 and GABRA5 alter receptor function and contribute to early-onset epilepsyKameryn M Butler, Olivia A Moody, Elisabeth Schuler, et al.
American Journal of Human Genetics|November 16, 2016
Reassessment of Genomic Sequence Variation to Harmonize Interpretation for Personalized MedicineKathryn B Garber, Lisa M Vincent, John J Alexander, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Advances in Experimental Medicine and Biology|January 15, 2008
Adeno-associated viral vectors and the retinaJohn J Alexander, William W Hauswirth
Drug News & Perspectives|July 4, 2008
Prospects for retinal cone-targeted gene therapyJohn J Alexander, William W Hauswirth
Journal of Child Neurology|September 15, 2006
Stroke associated with central nervous system vasculitis after West Nile virus infectionJohn J Alexander, Andrew S Lasky, William D Graf
American Journal of Medical Genetics. Part A|July 29, 2018
Is exon 8 the most critical or the only dispensable exon of the VCAN gene? Insights into VCAN variants and clinical spectrum of Wagner syndromeArunkanth Ankala, Nieraj Jain, Baker Hubbard, et al.
Pediatric Neurology|October 24, 2017
Diagnostic Yield From 339 Epilepsy Patients Screened on a Clinical Gene PanelKameryn M Butler, Cristina da Silva, John J Alexander, et al.
Pediatrics|October 8, 2008
Neuroimaging-use trends in nonacute pediatric headache before and after clinical practice parametersWilliam D Graf, Husam R Kayyali, John J Alexander, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 21, 2019
SubILM Injection of AAV for Gene Delivery to the RetinaPaul D Gamlin, John J Alexander, Sanford L Boye, et al.
Case Reports in Genetics|November 10, 2018
Epileptic Encephalopathy and Cerebellar Atrophy Resulting from Compound Heterozygous <i>CACNA2D2</i> VariantsKameryn M Butler, Philip J Holt, Sarah S Milla, et al.
Brain : a Journal of Neurology|July 3, 2018
De novo variants in GABRA2 and GABRA5 alter receptor function and contribute to early-onset epilepsyKameryn M Butler, Olivia A Moody, Elisabeth Schuler, et al.
American Journal of Human Genetics|November 16, 2016
Reassessment of Genomic Sequence Variation to Harmonize Interpretation for Personalized MedicineKathryn B Garber, Lisa M Vincent, John J Alexander, et al.
Pageof 4