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

R Baumgartner

Showing results (621-630 of 770) with videos related to

Pageof 77
Sort By:
Biochimica Et Biophysica Acta. Molecular Basis of Disease|June 20, 2021
Absence of MMACHC in peripheral retinal cells does not lead to an ocular phenotype in miceEva Kiessling, Sarah Nötzli, Vyara Todorova, et al.
Behavioural Brain Research|November 29, 2019
Sensitivity to gains during risky decision-making differentiates chronic cocaine users from stimulant-naïve controlsB Kluwe-Schiavon, A Kexel, G Manenti, et al.
European Journal of Pediatrics|June 5, 2001
Clinical and neuropsychological outcome in 33 patients with biotinidase deficiency ascertained by nationwide newborn screening and family studies in AustriaD Möslinger, S Stöckler-Ipsiroglu, S Scheibenreiter, et al.
Public Health Reports (Washington, D.C. : 1974)|March 6, 2021
Columbia University Master of Public Health Core Curriculum: Implementation, Student Experience, and Learning Outcomes, 2013-2018Samantha Garbers, Dana March, Julie Kornfeld, et al.
Neurology|November 18, 1998
Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann diseaseM R Baumgartner, N M Verhoeven, C Jakobs, et al.
Addiction Biology|January 21, 2015
Glutamatergic and neurometabolic alterations in chronic cocaine users measured with (1) H-magnetic resonance spectroscopyLea M Hulka, Milan Scheidegger, Matthias Vonmoos, et al.
International Journal of Cardiology. Heart & Vessels|February 17, 2018
Cardiac disease in children and young adults with various lysosomal storage diseases: Comparison of echocardiographic and ECG changes among clinical groupsP Mueller, C H Attenhofer Jost, M Rohrbach, et al.
Human Molecular Genetics|November 25, 2000
Hyperammonemia with reduced ornithine, citrulline, arginine and proline: a new inborn error caused by a mutation in the gene encoding delta(1)-pyrroline-5-carboxylate synthaseM R Baumgartner, C A Hu, S Almashanu, et al.
Plos One|September 16, 2017
Simultaneous determination of 3-hydroxypropionic acid, methylmalonic acid and methylcitric acid in dried blood spots: Second-tier LC-MS/MS assay for newborn screening of propionic acidemia, methylmalonic acidemias and combined remethylation disordersPéter Monostori, Glynis Klinke, Sylvia Richter, et al.
Comprehensive Psychoneuroendocrinology|November 17, 2022
Associations of different hormonal contraceptive methods with hair concentrations of cortisol, cortisone, and testosterone in young womenMariana Carrillo Vázquez, Lydia Johnson-Ferguson, Josua Zimmermann, et al.
Pageof 77

Showing results (621-630 of 770) with videos related to

Sort By:
Pageof 77
Biochimica Et Biophysica Acta. Molecular Basis of Disease|June 20, 2021
Absence of MMACHC in peripheral retinal cells does not lead to an ocular phenotype in miceEva Kiessling, Sarah Nötzli, Vyara Todorova, et al.
Behavioural Brain Research|November 29, 2019
Sensitivity to gains during risky decision-making differentiates chronic cocaine users from stimulant-naïve controlsB Kluwe-Schiavon, A Kexel, G Manenti, et al.
European Journal of Pediatrics|June 5, 2001
Clinical and neuropsychological outcome in 33 patients with biotinidase deficiency ascertained by nationwide newborn screening and family studies in AustriaD Möslinger, S Stöckler-Ipsiroglu, S Scheibenreiter, et al.
Public Health Reports (Washington, D.C. : 1974)|March 6, 2021
Columbia University Master of Public Health Core Curriculum: Implementation, Student Experience, and Learning Outcomes, 2013-2018Samantha Garbers, Dana March, Julie Kornfeld, et al.
Neurology|November 18, 1998
Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann diseaseM R Baumgartner, N M Verhoeven, C Jakobs, et al.
Addiction Biology|January 21, 2015
Glutamatergic and neurometabolic alterations in chronic cocaine users measured with (1) H-magnetic resonance spectroscopyLea M Hulka, Milan Scheidegger, Matthias Vonmoos, et al.
International Journal of Cardiology. Heart & Vessels|February 17, 2018
Cardiac disease in children and young adults with various lysosomal storage diseases: Comparison of echocardiographic and ECG changes among clinical groupsP Mueller, C H Attenhofer Jost, M Rohrbach, et al.
Human Molecular Genetics|November 25, 2000
Hyperammonemia with reduced ornithine, citrulline, arginine and proline: a new inborn error caused by a mutation in the gene encoding delta(1)-pyrroline-5-carboxylate synthaseM R Baumgartner, C A Hu, S Almashanu, et al.
Plos One|September 16, 2017
Simultaneous determination of 3-hydroxypropionic acid, methylmalonic acid and methylcitric acid in dried blood spots: Second-tier LC-MS/MS assay for newborn screening of propionic acidemia, methylmalonic acidemias and combined remethylation disordersPéter Monostori, Glynis Klinke, Sylvia Richter, et al.
Comprehensive Psychoneuroendocrinology|November 17, 2022
Associations of different hormonal contraceptive methods with hair concentrations of cortisol, cortisone, and testosterone in young womenMariana Carrillo Vázquez, Lydia Johnson-Ferguson, Josua Zimmermann, et al.
Pageof 77