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

E Christ

Showing results (151-160 of 162) with videos related to

Pageof 17
Sort By:
Neuropsychology|March 24, 2020
Executive function in phenylketonuria (PKU): Insights from the Behavior Rating Inventory of Executive Function (BRIEF) and a large sample of individuals with PKUShawn E Christ, Hayley E Clocksin, Barbara K Burton, et al.
Journal of Endocrinological Investigation|April 13, 2021
First-line surgery in prolactinomas: lessons from a long-term follow-up study in a tertiary referral centerL Andereggen, J Frey, R H Andres, et al.
Pediatrics|June 1, 1997
Prevalence of retinal hemorrhages in pediatric patients after in-hospital cardiopulmonary resuscitation: a prospective studyA Odom, E Christ, N Kerr, et al.
Journal of Neuroendocrinology|September 15, 2025
Controversies in NEN: An ENETS position statement on the management of locally advanced neuroendocrine neoplasia of the small intestine and pancreas without distant metastasesM E T Tesselaar, S Partelli, A J A T Braat, et al.
Molecular Genetics and Metabolism|December 8, 2014
Prolonged exposure to high and variable phenylalanine levels over the lifetime predicts brain white matter integrity in children with phenylketonuriaAnna Hood, Jo Ann V Antenor-Dorsey, Jerrel Rutlin, et al.
Molecular Genetics and Metabolism|July 26, 2024
Initial results from the PHEFREE longitudinal natural history study: Cross-sectional observations in a cohort of individuals with phenylalanine hydroxylase (PAH) deficiencyShawn E Christ, Georgianne Arnold, Uta Lichter-Konecki, et al.
The American Journal of Clinical Nutrition|March 5, 2025
Phenylketonuria in adults: we know plenty, but there is much more to learnCary O Harding, Georgianne Arnold, Gerard T Berry, et al.
Molecular Genetics and Metabolism|August 1, 2024
Neurocognitive assessment platform for clinical trials in PKU: White paper developed by the NPKUA neurocognitive workgroupSusan E Waisbren, Shawn E Christ, Deborah A Bilder, et al.
Environmental Science. Processes & Impacts|October 2, 2023
Chemical characterization of microplastic particles formed in airborne waste discharged from sewer pipe repairsBrianna N Peterson, Ana C Morales, Jay M Tomlin, et al.
Molecular Genetics and Metabolism|August 26, 2022
Management of early treated adolescents and young adults with phenylketonuria: Development of international consensus recommendations using a modified Delphi approachBarbara K Burton, Álvaro Hermida, Amaya Bélanger-Quintana, et al.
Pageof 17

Showing results (151-160 of 162) with videos related to

Sort By:
Pageof 17
Neuropsychology|March 24, 2020
Executive function in phenylketonuria (PKU): Insights from the Behavior Rating Inventory of Executive Function (BRIEF) and a large sample of individuals with PKUShawn E Christ, Hayley E Clocksin, Barbara K Burton, et al.
Journal of Endocrinological Investigation|April 13, 2021
First-line surgery in prolactinomas: lessons from a long-term follow-up study in a tertiary referral centerL Andereggen, J Frey, R H Andres, et al.
Pediatrics|June 1, 1997
Prevalence of retinal hemorrhages in pediatric patients after in-hospital cardiopulmonary resuscitation: a prospective studyA Odom, E Christ, N Kerr, et al.
Journal of Neuroendocrinology|September 15, 2025
Controversies in NEN: An ENETS position statement on the management of locally advanced neuroendocrine neoplasia of the small intestine and pancreas without distant metastasesM E T Tesselaar, S Partelli, A J A T Braat, et al.
Molecular Genetics and Metabolism|December 8, 2014
Prolonged exposure to high and variable phenylalanine levels over the lifetime predicts brain white matter integrity in children with phenylketonuriaAnna Hood, Jo Ann V Antenor-Dorsey, Jerrel Rutlin, et al.
Molecular Genetics and Metabolism|July 26, 2024
Initial results from the PHEFREE longitudinal natural history study: Cross-sectional observations in a cohort of individuals with phenylalanine hydroxylase (PAH) deficiencyShawn E Christ, Georgianne Arnold, Uta Lichter-Konecki, et al.
The American Journal of Clinical Nutrition|March 5, 2025
Phenylketonuria in adults: we know plenty, but there is much more to learnCary O Harding, Georgianne Arnold, Gerard T Berry, et al.
Molecular Genetics and Metabolism|August 1, 2024
Neurocognitive assessment platform for clinical trials in PKU: White paper developed by the NPKUA neurocognitive workgroupSusan E Waisbren, Shawn E Christ, Deborah A Bilder, et al.
Environmental Science. Processes & Impacts|October 2, 2023
Chemical characterization of microplastic particles formed in airborne waste discharged from sewer pipe repairsBrianna N Peterson, Ana C Morales, Jay M Tomlin, et al.
Molecular Genetics and Metabolism|August 26, 2022
Management of early treated adolescents and young adults with phenylketonuria: Development of international consensus recommendations using a modified Delphi approachBarbara K Burton, Álvaro Hermida, Amaya Bélanger-Quintana, et al.
Pageof 17