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

Laura E Case

Showing results (21-30 of 57) with videos related to

Pageof 6
Sort By:
Pediatrics|October 3, 2018
Rehabilitation Management of the Patient With Duchenne Muscular DystrophyLaura E Case, Susan D Apkon, Michelle Eagle, et al.
Molecular Genetics and Metabolism|September 21, 2011
The prevalence and impact of scoliosis in Pompe disease: lessons learned from the Pompe RegistryMark Roberts, Priya S Kishnani, Ans T van der Ploeg, et al.
Molecular Genetics and Metabolism|October 15, 2021
Physical therapy assessment and whole-body magnetic resonance imaging findings in children with glycogen storage disease type IIIa: A clinical study and review of the literatureAnna Paschall, Aleena A Khan, Syed Faaiz Enam, et al.
Molecular Genetics and Metabolism|July 9, 2016
Physical therapy management of infants and children with hypophosphatasiaDawn Phillips, Laura E Case, Donna Griffin, et al.
Pediatrics|October 3, 2018
A Transition Toolkit for Duchenne Muscular DystrophyChristina J Trout, Laura E Case, Paula R Clemens, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 21, 2014
Adjunctive albuterol enhances the response to enzyme replacement therapy in late-onset Pompe diseaseDwight D Koeberl, Stephanie Austin, Laura E Case, et al.
Stem Cells Translational Medicine|June 4, 2021
Sibling umbilical cord blood infusion is safe in young children with cerebral palsyJessica M Sun, Laura E Case, Mohamad A Mikati, et al.
Developmental Medicine and Child Neurology|July 11, 2022
Motor function and safety after allogeneic cord blood and cord tissue-derived mesenchymal stromal cells in cerebral palsy: An open-label, randomized trialJessica M Sun, Laura E Case, Colleen McLaughlin, et al.
Molecular Genetics and Metabolism|October 16, 2012
Bulbar muscle weakness and fatty lingual infiltration in glycogen storage disorder type IIIaJeffrey J Horvath, Stephanie L Austin, Harrison N Jones, et al.
Molecular Genetics and Metabolism|September 27, 2025
Quantitative muscle ultrasound as a window into disease progression in infantile-onset Pompe diseaseNeelam Makhijani, Myriam Boueri, Bijan Abar, et al.
Pageof 6

Showing results (21-30 of 57) with videos related to

Sort By:
Pageof 6
Pediatrics|October 3, 2018
Rehabilitation Management of the Patient With Duchenne Muscular DystrophyLaura E Case, Susan D Apkon, Michelle Eagle, et al.
Molecular Genetics and Metabolism|September 21, 2011
The prevalence and impact of scoliosis in Pompe disease: lessons learned from the Pompe RegistryMark Roberts, Priya S Kishnani, Ans T van der Ploeg, et al.
Molecular Genetics and Metabolism|October 15, 2021
Physical therapy assessment and whole-body magnetic resonance imaging findings in children with glycogen storage disease type IIIa: A clinical study and review of the literatureAnna Paschall, Aleena A Khan, Syed Faaiz Enam, et al.
Molecular Genetics and Metabolism|July 9, 2016
Physical therapy management of infants and children with hypophosphatasiaDawn Phillips, Laura E Case, Donna Griffin, et al.
Pediatrics|October 3, 2018
A Transition Toolkit for Duchenne Muscular DystrophyChristina J Trout, Laura E Case, Paula R Clemens, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 21, 2014
Adjunctive albuterol enhances the response to enzyme replacement therapy in late-onset Pompe diseaseDwight D Koeberl, Stephanie Austin, Laura E Case, et al.
Stem Cells Translational Medicine|June 4, 2021
Sibling umbilical cord blood infusion is safe in young children with cerebral palsyJessica M Sun, Laura E Case, Mohamad A Mikati, et al.
Developmental Medicine and Child Neurology|July 11, 2022
Motor function and safety after allogeneic cord blood and cord tissue-derived mesenchymal stromal cells in cerebral palsy: An open-label, randomized trialJessica M Sun, Laura E Case, Colleen McLaughlin, et al.
Molecular Genetics and Metabolism|October 16, 2012
Bulbar muscle weakness and fatty lingual infiltration in glycogen storage disorder type IIIaJeffrey J Horvath, Stephanie L Austin, Harrison N Jones, et al.
Molecular Genetics and Metabolism|September 27, 2025
Quantitative muscle ultrasound as a window into disease progression in infantile-onset Pompe diseaseNeelam Makhijani, Myriam Boueri, Bijan Abar, et al.
Pageof 6