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

Mary Seeterlin

Showing results (1-10 of 5) with videos related to

Pageof 1
Sort By:
JIMD Reports|February 23, 2013
Case Report of Argininemia: The Utility of the Arginine/Ornithine Ratio for Newborn Screening (NBS)Allison Jay, Mary Seeterlin, Eleanor Stanley, et al.
European Journal of Medical Genetics|September 27, 2020
Methionine adenosyltransferase I/III deficiency: Long-term follow-up and treatment of 3 adult siblingsAllison Bannick, Sara Chase, Alyson Miner, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
Newborn screening for dihydrolipoamide dehydrogenase deficiency: Citrulline as a useful analyteShane C Quinonez, Andrea H Seeley, Mary Seeterlin, et al.
International Journal of Neonatal Screening|October 30, 2020
Harmonizing Newborn Screening Laboratory Proficiency Test Results Using the CDC NSQAP Reference MaterialsCharles Austin Pickens, Maya Sternberg, Mary Seeterlin, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 2015
Heptadecanoylcarnitine (C17) a novel candidate biomarker for newborn screening of propionic and methylmalonic acidemiasSabrina Malvagia, Christopher A Haynes, Laura Grisotto, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
JIMD Reports|February 23, 2013
Case Report of Argininemia: The Utility of the Arginine/Ornithine Ratio for Newborn Screening (NBS)Allison Jay, Mary Seeterlin, Eleanor Stanley, et al.
European Journal of Medical Genetics|September 27, 2020
Methionine adenosyltransferase I/III deficiency: Long-term follow-up and treatment of 3 adult siblingsAllison Bannick, Sara Chase, Alyson Miner, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
Newborn screening for dihydrolipoamide dehydrogenase deficiency: Citrulline as a useful analyteShane C Quinonez, Andrea H Seeley, Mary Seeterlin, et al.
International Journal of Neonatal Screening|October 30, 2020
Harmonizing Newborn Screening Laboratory Proficiency Test Results Using the CDC NSQAP Reference MaterialsCharles Austin Pickens, Maya Sternberg, Mary Seeterlin, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 2015
Heptadecanoylcarnitine (C17) a novel candidate biomarker for newborn screening of propionic and methylmalonic acidemiasSabrina Malvagia, Christopher A Haynes, Laura Grisotto, et al.
Pageof 1