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

Priya S Kishnani

Showing results (1-10 of 368) with videos related to

Pageof 37
Sort By:
Current Gene Therapy|October 8, 2009
Immunomodulatory gene therapy in lysosomal storage disordersDwight D Koeberl, Priya S Kishnani
Pediatric Endocrinology Reviews : PER|October 28, 2014
New therapeutic approaches for Pompe disease: enzyme replacement therapy and beyondPriya S Kishnani, Alexandra A Beckemeyer
Pediatrics|November 23, 2017
Introduction to the Newborn Screening, Diagnosis, and Treatment for Pompe Disease Guidance SupplementPriya S Kishnani, Wuh-Liang Hwu,
Annals of Translational Medicine|August 9, 2019
Liver depot gene therapy for Pompe diseasePriya S Kishnani, Dwight D Koeberl
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 19, 2006
Clinical manifestations of hematologic and oncologic disorders in patients with Down syndromeNatalia Dixon, Priya S Kishnani, Sherri Zimmerman
Muscle & Nerve|January 17, 2012
How common is misdiagnosis in late-onset Pompe disease?Lisa D Hobson-Webb, Priya S Kishnani
Molecular Genetics and Metabolism Reports|November 30, 2016
Right frontal lobe encephalomalacia in an adult propionic acidemia patient with neuropsychiatric manifestationsPankaj Prasun, Lauren A Bailey, Priya S Kishnani
JCI Insight|October 20, 2022
Suppression of pullulanase-induced cytotoxic T cell response with a dual promoter in GSD IIIa miceJeong-A Lim, Priya S Kishnani, Baodong Sun
Human Molecular Genetics|June 23, 2019
Gene therapy for glycogen storage diseasesPriya S Kishnani, Baodong Sun, Dwight D Koeberl
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 19, 2012
The new era of Pompe disease: advances in the detection, understanding of the phenotypic spectrum, pathophysiology, and managementPriya S Kishnani, Alexandra A Beckemeyer, Nancy J Mendelsohn
Pageof 37

Showing results (1-10 of 368) with videos related to

Sort By:
Pageof 37
Current Gene Therapy|October 8, 2009
Immunomodulatory gene therapy in lysosomal storage disordersDwight D Koeberl, Priya S Kishnani
Pediatric Endocrinology Reviews : PER|October 28, 2014
New therapeutic approaches for Pompe disease: enzyme replacement therapy and beyondPriya S Kishnani, Alexandra A Beckemeyer
Pediatrics|November 23, 2017
Introduction to the Newborn Screening, Diagnosis, and Treatment for Pompe Disease Guidance SupplementPriya S Kishnani, Wuh-Liang Hwu,
Annals of Translational Medicine|August 9, 2019
Liver depot gene therapy for Pompe diseasePriya S Kishnani, Dwight D Koeberl
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 19, 2006
Clinical manifestations of hematologic and oncologic disorders in patients with Down syndromeNatalia Dixon, Priya S Kishnani, Sherri Zimmerman
Muscle & Nerve|January 17, 2012
How common is misdiagnosis in late-onset Pompe disease?Lisa D Hobson-Webb, Priya S Kishnani
Molecular Genetics and Metabolism Reports|November 30, 2016
Right frontal lobe encephalomalacia in an adult propionic acidemia patient with neuropsychiatric manifestationsPankaj Prasun, Lauren A Bailey, Priya S Kishnani
JCI Insight|October 20, 2022
Suppression of pullulanase-induced cytotoxic T cell response with a dual promoter in GSD IIIa miceJeong-A Lim, Priya S Kishnani, Baodong Sun
Human Molecular Genetics|June 23, 2019
Gene therapy for glycogen storage diseasesPriya S Kishnani, Baodong Sun, Dwight D Koeberl
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 19, 2012
The new era of Pompe disease: advances in the detection, understanding of the phenotypic spectrum, pathophysiology, and managementPriya S Kishnani, Alexandra A Beckemeyer, Nancy J Mendelsohn
Pageof 37