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R Baumgartner

Showing results (521-530 of 770) with videos related to

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European Journal of Pediatrics|May 1, 1996
Atypical vitamin B12-unresponsive methylmalonic aciduria in sibship with severe progressive encephalomyelopathy: a new genetic disease?E Mayatepek, G F Hoffmann, R Baumgartner, et al.
Molecular Genetics and Metabolism|October 26, 2019
Tricarboxylic acid cycle enzyme activities in a mouse model of methylmalonic aciduriaParith Wongkittichote, Gary Cunningham, Marshall L Summar, et al.
Molecular Genetics and Metabolism|May 15, 2001
Mutation analysis of the MCM gene in Israeli patients with mut(0) diseaseI Berger, A Shaag, Y Anikster, et al.
European Journal of Pediatrics|September 15, 1999
Metabolic stroke in isolated 3-methylcrotonyl-CoA carboxylase deficiencyC Steen, E R Baumgartner, M Duran, et al.
Journal of Inherited Metabolic Disease|October 13, 2001
CblC/D defect combined with haemodynamically highly relevant VSDM Tomaske, A Bosk, M K Heinemann, et al.
Journal of Inherited Metabolic Disease|May 16, 2020
Organic acidurias: Major gaps, new challenges, and a yet unfulfilled promiseBianca Dimitrov, Femke Molema, Monique Williams, et al.
Archives of General Psychiatry|November 1, 1984
Haloperidol. Plasma levels and prolactin response as predictors of clinical improvement in schizophrenia: chemical v radioreceptor plasma level assaysR C Smith, R Baumgartner, C H Misra, et al.
Biomed Research International|March 31, 2015
An open-label uncontrolled, multicenter study for the evaluation of the efficacy and safety of the dermal filler Princess VOLUME in the treatment of nasolabial foldsDaisy Kopera, Michael Palatin, Rolf Bartsch, et al.
BMC Veterinary Research|June 24, 2016
Erratum to: Long-term monitoring of opioid, sedative and anti-inflammatory drugs in horse hair using a selective and sensitive LC-MS/MS procedureMilena M Madry, Barbara S Spycher, Jacqueline Kupper, et al.
Journal of Inherited Metabolic Disease|March 13, 2015
Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelinesMartina Huemer, Viktor Kožich, Piero Rinaldo, et al.
Pageof 77

Showing results (521-530 of 770) with videos related to

Sort By:
Pageof 77
European Journal of Pediatrics|May 1, 1996
Atypical vitamin B12-unresponsive methylmalonic aciduria in sibship with severe progressive encephalomyelopathy: a new genetic disease?E Mayatepek, G F Hoffmann, R Baumgartner, et al.
Molecular Genetics and Metabolism|October 26, 2019
Tricarboxylic acid cycle enzyme activities in a mouse model of methylmalonic aciduriaParith Wongkittichote, Gary Cunningham, Marshall L Summar, et al.
Molecular Genetics and Metabolism|May 15, 2001
Mutation analysis of the MCM gene in Israeli patients with mut(0) diseaseI Berger, A Shaag, Y Anikster, et al.
European Journal of Pediatrics|September 15, 1999
Metabolic stroke in isolated 3-methylcrotonyl-CoA carboxylase deficiencyC Steen, E R Baumgartner, M Duran, et al.
Journal of Inherited Metabolic Disease|October 13, 2001
CblC/D defect combined with haemodynamically highly relevant VSDM Tomaske, A Bosk, M K Heinemann, et al.
Journal of Inherited Metabolic Disease|May 16, 2020
Organic acidurias: Major gaps, new challenges, and a yet unfulfilled promiseBianca Dimitrov, Femke Molema, Monique Williams, et al.
Archives of General Psychiatry|November 1, 1984
Haloperidol. Plasma levels and prolactin response as predictors of clinical improvement in schizophrenia: chemical v radioreceptor plasma level assaysR C Smith, R Baumgartner, C H Misra, et al.
Biomed Research International|March 31, 2015
An open-label uncontrolled, multicenter study for the evaluation of the efficacy and safety of the dermal filler Princess VOLUME in the treatment of nasolabial foldsDaisy Kopera, Michael Palatin, Rolf Bartsch, et al.
BMC Veterinary Research|June 24, 2016
Erratum to: Long-term monitoring of opioid, sedative and anti-inflammatory drugs in horse hair using a selective and sensitive LC-MS/MS procedureMilena M Madry, Barbara S Spycher, Jacqueline Kupper, et al.
Journal of Inherited Metabolic Disease|March 13, 2015
Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelinesMartina Huemer, Viktor Kožich, Piero Rinaldo, et al.
Pageof 77