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

Peter Bauer

Showing results (221-230 of 585) with videos related to

Pageof 59
Sort By:
International Journal of Molecular Sciences|February 25, 2023
Contribution of Glucosylsphingosine (Lyso-Gb1) to Treatment Decisions in Patients with Gaucher DiseaseTama Dinur, Peter Bauer, Christian Beetz, et al.
European Journal of Human Genetics : EJHG|October 13, 2006
Repeat expansion in spinocerebellar ataxia type 17 alleles of the TATA-box binding protein gene: an evolutionary approachJürgen Tomiuk, Lutz Bachmann, Claudia Bauer, et al.
Caries Research|May 23, 2015
Lactotransferrin Gene Polymorphism Associated with Caries ExperienceAndrea D Doetzer, João A Brancher, Giovana D Pecharki, et al.
Neurology. Genetics|June 30, 2025
A Retrospective Cohort Study of the GLA c.937G > T, p.Asp313Tyr Variant With No Evidence of an Association With Fabry DiseaseTobias Boettcher, Christian Beetz, Daniel Schulze, et al.
NPJ Parkinson'S Disease|January 10, 2026
Metabolomic breath landscape analysis unravels lipid biomarker candidates in patients with genetic and idiopathic Parkinson's diseaseMadiha Malik, Norbert Brüggemann, Tatiana Usnich, et al.
Allergy|December 15, 2020
Long-term effects of hydrolyzed formulae on atopic diseases in the GINI studyMonika Gappa, Birgit Filipiak-Pittroff, Lars Libuda, et al.
Journal of Neurology|March 13, 2024
Moyamoya disease in Southeast Asians: genetic and autopsy data, new cases, systematic review, and meta-analysis of all patients from the literatureDaniel Strunk, Peter Bauer, Kathy Keyvani, et al.
Scientific Reports|October 30, 2023
Neuronal progenitor cells-based metabolomics study reveals dysregulated lipid metabolism and identifies putative biomarkers for CLN6 diseaseCorina-Marcela Rus, Daniel L Polla, Sebastiano Di Bucchianico, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|October 20, 2005
Diagnostic value of quantitative hepatic copper determination in patients with Wilson's DiseasePeter Ferenci, Petra Steindl-Munda, Wolfgang Vogel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 18, 2015
Mutations in CIZ1 are not a major cause for dystonia in GermanyClaudia Dufke, Ann-Kathrin Hauser, Marc Sturm, et al.
Pageof 59

Showing results (221-230 of 585) with videos related to

Sort By:
Pageof 59
International Journal of Molecular Sciences|February 25, 2023
Contribution of Glucosylsphingosine (Lyso-Gb1) to Treatment Decisions in Patients with Gaucher DiseaseTama Dinur, Peter Bauer, Christian Beetz, et al.
European Journal of Human Genetics : EJHG|October 13, 2006
Repeat expansion in spinocerebellar ataxia type 17 alleles of the TATA-box binding protein gene: an evolutionary approachJürgen Tomiuk, Lutz Bachmann, Claudia Bauer, et al.
Caries Research|May 23, 2015
Lactotransferrin Gene Polymorphism Associated with Caries ExperienceAndrea D Doetzer, João A Brancher, Giovana D Pecharki, et al.
Neurology. Genetics|June 30, 2025
A Retrospective Cohort Study of the GLA c.937G > T, p.Asp313Tyr Variant With No Evidence of an Association With Fabry DiseaseTobias Boettcher, Christian Beetz, Daniel Schulze, et al.
NPJ Parkinson'S Disease|January 10, 2026
Metabolomic breath landscape analysis unravels lipid biomarker candidates in patients with genetic and idiopathic Parkinson's diseaseMadiha Malik, Norbert Brüggemann, Tatiana Usnich, et al.
Allergy|December 15, 2020
Long-term effects of hydrolyzed formulae on atopic diseases in the GINI studyMonika Gappa, Birgit Filipiak-Pittroff, Lars Libuda, et al.
Journal of Neurology|March 13, 2024
Moyamoya disease in Southeast Asians: genetic and autopsy data, new cases, systematic review, and meta-analysis of all patients from the literatureDaniel Strunk, Peter Bauer, Kathy Keyvani, et al.
Scientific Reports|October 30, 2023
Neuronal progenitor cells-based metabolomics study reveals dysregulated lipid metabolism and identifies putative biomarkers for CLN6 diseaseCorina-Marcela Rus, Daniel L Polla, Sebastiano Di Bucchianico, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|October 20, 2005
Diagnostic value of quantitative hepatic copper determination in patients with Wilson's DiseasePeter Ferenci, Petra Steindl-Munda, Wolfgang Vogel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 18, 2015
Mutations in CIZ1 are not a major cause for dystonia in GermanyClaudia Dufke, Ann-Kathrin Hauser, Marc Sturm, et al.
Pageof 59