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

M Maier

Showing results (851-860 of 863) with videos related to

Pageof 87
Sort By:
Pediatric Research|April 28, 2006
Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiencyStefan Kölker, Sven F Garbade, Cheryl R Greenberg, et al.
Journal of Inherited Metabolic Disease|September 2, 2022
Impact of pregnancy planning and preconceptual dietary training on metabolic control and offspring's outcome in phenylketonuriaKarina Grohmann-Held, Peter Burgard, Christoph G O Baerwald, et al.
Journal of Inherited Metabolic Disease|October 11, 2022
Recommendations for diagnosing and managing individuals with glutaric aciduria type 1: Third revisionNikolas Boy, Chris Mühlhausen, Esther M Maier, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 7, 2022
An integrative skeletal and paleogenomic analysis of stature variation suggests relatively reduced health for early European farmersStephanie Marciniak, Christina M Bergey, Ana Maria Silva, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 22, 2021
Direct field evidence of autocatalytic iodine release from atmospheric aerosolYee Jun Tham, Xu-Cheng He, Qinyi Li, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 25, 2009
The role of the CD58 locus in multiple sclerosisPhilip L De Jager, Clare Baecher-Allan, Lisa M Maier, et al.
Journal of Medical Virology|December 29, 2019
A European multicentre evaluation of detection and typing methods for human enteroviruses and parechoviruses using RNA transcriptsA Hayes, D Nguyen, M Andersson, et al.
American Journal of Human Genetics|July 2, 2019
Mutations in PIGB Cause an Inherited GPI Biosynthesis Defect with an Axonal Neuropathy and Metabolic Abnormality in Severe CasesYoshiko Murakami, Thi Tuyet Mai Nguyen, Nissan Baratang, et al.
Brain : a Journal of Neurology|August 8, 2020
Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorderPauline E Schneeberger, Fanny Kortüm, Georg Christoph Korenke, et al.
Nature|July 15, 2026
Magnetic character of the low-energy enhancement in <sup>70</sup>ZnE K Ronning, A L Richard, S N Liddick, et al.
Pageof 87

Showing results (851-860 of 863) with videos related to

Sort By:
Pageof 87
Pediatric Research|April 28, 2006
Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiencyStefan Kölker, Sven F Garbade, Cheryl R Greenberg, et al.
Journal of Inherited Metabolic Disease|September 2, 2022
Impact of pregnancy planning and preconceptual dietary training on metabolic control and offspring's outcome in phenylketonuriaKarina Grohmann-Held, Peter Burgard, Christoph G O Baerwald, et al.
Journal of Inherited Metabolic Disease|October 11, 2022
Recommendations for diagnosing and managing individuals with glutaric aciduria type 1: Third revisionNikolas Boy, Chris Mühlhausen, Esther M Maier, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 7, 2022
An integrative skeletal and paleogenomic analysis of stature variation suggests relatively reduced health for early European farmersStephanie Marciniak, Christina M Bergey, Ana Maria Silva, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 22, 2021
Direct field evidence of autocatalytic iodine release from atmospheric aerosolYee Jun Tham, Xu-Cheng He, Qinyi Li, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 25, 2009
The role of the CD58 locus in multiple sclerosisPhilip L De Jager, Clare Baecher-Allan, Lisa M Maier, et al.
Journal of Medical Virology|December 29, 2019
A European multicentre evaluation of detection and typing methods for human enteroviruses and parechoviruses using RNA transcriptsA Hayes, D Nguyen, M Andersson, et al.
American Journal of Human Genetics|July 2, 2019
Mutations in PIGB Cause an Inherited GPI Biosynthesis Defect with an Axonal Neuropathy and Metabolic Abnormality in Severe CasesYoshiko Murakami, Thi Tuyet Mai Nguyen, Nissan Baratang, et al.
Brain : a Journal of Neurology|August 8, 2020
Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorderPauline E Schneeberger, Fanny Kortüm, Georg Christoph Korenke, et al.
Nature|July 15, 2026
Magnetic character of the low-energy enhancement in <sup>70</sup>ZnE K Ronning, A L Richard, S N Liddick, et al.
Pageof 87