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Ulrike Mütze

Showing results (1-10 of 52) with videos related to

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Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|October 10, 2023
[Evaluation and optimization of newborn screening by structured long-term follow-up-using the example of inherited metabolic diseases]Ulrike Mütze, Stefan Kölker
Frontiers in Endocrinology|March 23, 2022
Rare Disease Registries Are Key to Evidence-Based Personalized Medicine: Highlighting the European ExperienceStefan Kölker, Florian Gleich, Ulrike Mütze, et al.
Orphanet Journal of Rare Diseases|March 25, 2016
Ten years of specialized adult care for phenylketonuria - a single-centre experienceUlrike Mütze, Alena Gerlinde Thiele, Christoph Baerwald, et al.
JIMD Reports|April 18, 2022
Opportunities and challenges in machine learning-based newborn screening-A systematic literature reviewElaine Zaunseder, Saskia Haupt, Ulrike Mütze, et al.
Journal of Inherited Metabolic Disease|January 17, 2018
Organic acidurias in adults: late complications and managementAli Tunç Tuncel, Nikolas Boy, Marina A Morath, et al.
Journal of Inherited Metabolic Disease|April 30, 2022
How longitudinal observational studies can guide screening strategy for rare diseasesUlrike Mütze, Katharina Mengler, Nikolas Boy, et al.
Journal of Inherited Metabolic Disease|October 24, 2025
Trial Readiness: Understanding the Natural History of Rare DiseasesThomas Opladen, Ulrike Mütze, Florian Gleich, et al.
JIMD Reports|January 13, 2023
Neonatal screening for isovaleric aciduria: Reducing the increasingly high false-positive rate in GermanySimona Murko, Asra Dadkhah Aseman, Friederike Reinhardt, et al.
Cell Metabolism|June 4, 2024
Personalized metabolic whole-body models for newborns and infants predict growth and biomarkers of inherited metabolic diseasesElaine Zaunseder, Ulrike Mütze, Jürgen G Okun, et al.
Journal of Inherited Metabolic Disease|February 10, 2011
Transition of young adults with phenylketonuria from pediatric to adult careUlrike Mütze, Annika Roth, Johannes F W Weigel, et al.
Pageof 6

Showing results (1-10 of 52) with videos related to

Sort By:
Pageof 6
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|October 10, 2023
[Evaluation and optimization of newborn screening by structured long-term follow-up-using the example of inherited metabolic diseases]Ulrike Mütze, Stefan Kölker
Frontiers in Endocrinology|March 23, 2022
Rare Disease Registries Are Key to Evidence-Based Personalized Medicine: Highlighting the European ExperienceStefan Kölker, Florian Gleich, Ulrike Mütze, et al.
Orphanet Journal of Rare Diseases|March 25, 2016
Ten years of specialized adult care for phenylketonuria - a single-centre experienceUlrike Mütze, Alena Gerlinde Thiele, Christoph Baerwald, et al.
JIMD Reports|April 18, 2022
Opportunities and challenges in machine learning-based newborn screening-A systematic literature reviewElaine Zaunseder, Saskia Haupt, Ulrike Mütze, et al.
Journal of Inherited Metabolic Disease|January 17, 2018
Organic acidurias in adults: late complications and managementAli Tunç Tuncel, Nikolas Boy, Marina A Morath, et al.
Journal of Inherited Metabolic Disease|April 30, 2022
How longitudinal observational studies can guide screening strategy for rare diseasesUlrike Mütze, Katharina Mengler, Nikolas Boy, et al.
Journal of Inherited Metabolic Disease|October 24, 2025
Trial Readiness: Understanding the Natural History of Rare DiseasesThomas Opladen, Ulrike Mütze, Florian Gleich, et al.
JIMD Reports|January 13, 2023
Neonatal screening for isovaleric aciduria: Reducing the increasingly high false-positive rate in GermanySimona Murko, Asra Dadkhah Aseman, Friederike Reinhardt, et al.
Cell Metabolism|June 4, 2024
Personalized metabolic whole-body models for newborns and infants predict growth and biomarkers of inherited metabolic diseasesElaine Zaunseder, Ulrike Mütze, Jürgen G Okun, et al.
Journal of Inherited Metabolic Disease|February 10, 2011
Transition of young adults with phenylketonuria from pediatric to adult careUlrike Mütze, Annika Roth, Johannes F W Weigel, et al.
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