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

Barbara K Burton

Showing results (1-10 of 122) with videos related to

Pageof 13
Sort By:
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 19, 2012
Newborn screening for Pompe disease: an update, 2011Barbara K Burton
European Journal of Pediatrics|March 3, 2012
Diagnosing Hunter syndrome in pediatric practice: practical considerations and common pitfallsBarbara K Burton, Roberto Giugliani
Molecular Genetics and Metabolism|November 3, 2007
Risk of sudden death and acute life-threatening events in patients with glutaric acidemia type IIBrad Angle, Barbara K Burton
American Journal of Medical Genetics. Part A|June 9, 2012
Survey of health status and complications among propionic acidemia patientsLoren Pena, Barbara K Burton
Molecular Genetics and Metabolism|July 20, 2010
Reaching out to the lost generation of adults with early-treated phenylketonuria (PKU)Barbara K Burton, Lauren Leviton
Molecular Genetics and Metabolism|November 19, 2013
Increased incidence of neonatal respiratory distress in infants with mucopolysaccharidosis type II (MPS II, Hunter syndrome)Charlotte Dodsworth, Barbara K Burton
Touchreviews in Endocrinology|February 4, 2022
Diagnosis and Clinical Management of Long-chain Fatty-acid Oxidation Disorders: A ReviewJoshua J Baker, Barbara K Burton
Current Medical Research and Opinion|March 22, 2017
Progression of liver disease in children and adults with lysosomal acid lipase deficiencyBarbara K Burton, Nancy Silliman, Sachin Marulkar
Molecular Genetics and Metabolism|March 29, 2011
Incidence and timing of infusion-related reactions in patients with mucopolysaccharidosis type II (Hunter syndrome) on idursulfase therapy in the real-world setting: a perspective from the Hunter Outcome Survey (HOS)Barbara K Burton, David A H Whiteman,
International Journal of Neonatal Screening|October 29, 2020
Newborn Screening for Mucopolysaccharidosis Type II in Illinois: An UpdateBarbara K Burton, Rachel Hickey, Lauren Hitchins
Pageof 13

Showing results (1-10 of 122) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 19, 2012
Newborn screening for Pompe disease: an update, 2011Barbara K Burton
European Journal of Pediatrics|March 3, 2012
Diagnosing Hunter syndrome in pediatric practice: practical considerations and common pitfallsBarbara K Burton, Roberto Giugliani
Molecular Genetics and Metabolism|November 3, 2007
Risk of sudden death and acute life-threatening events in patients with glutaric acidemia type IIBrad Angle, Barbara K Burton
American Journal of Medical Genetics. Part A|June 9, 2012
Survey of health status and complications among propionic acidemia patientsLoren Pena, Barbara K Burton
Molecular Genetics and Metabolism|July 20, 2010
Reaching out to the lost generation of adults with early-treated phenylketonuria (PKU)Barbara K Burton, Lauren Leviton
Molecular Genetics and Metabolism|November 19, 2013
Increased incidence of neonatal respiratory distress in infants with mucopolysaccharidosis type II (MPS II, Hunter syndrome)Charlotte Dodsworth, Barbara K Burton
Touchreviews in Endocrinology|February 4, 2022
Diagnosis and Clinical Management of Long-chain Fatty-acid Oxidation Disorders: A ReviewJoshua J Baker, Barbara K Burton
Current Medical Research and Opinion|March 22, 2017
Progression of liver disease in children and adults with lysosomal acid lipase deficiencyBarbara K Burton, Nancy Silliman, Sachin Marulkar
Molecular Genetics and Metabolism|March 29, 2011
Incidence and timing of infusion-related reactions in patients with mucopolysaccharidosis type II (Hunter syndrome) on idursulfase therapy in the real-world setting: a perspective from the Hunter Outcome Survey (HOS)Barbara K Burton, David A H Whiteman,
International Journal of Neonatal Screening|October 29, 2020
Newborn Screening for Mucopolysaccharidosis Type II in Illinois: An UpdateBarbara K Burton, Rachel Hickey, Lauren Hitchins
Pageof 13