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R Baumgartner

Showing results (601-610 of 770) with videos related to

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The International Journal of Neuropsychopharmacology|November 1, 2017
Social Cognition and Interaction in Chronic Users of 3,4-Methylenedioxymethamphetamine (MDMA, "Ecstasy")Michael D Wunderli, Matthias Vonmoos, Lorena Treichler, et al.
European Journal of Pediatrics|March 1, 1990
Methylmalonic aciduria with homocystinuria: biochemical studies, treatment, and clinical course of a Cbl-C patientA Ribes, P Briones, M A Vilaseca, et al.
JIMD Reports|March 6, 2024
Non-Hodgkin lymphoma in a kidney transplanted patient with methylmalonic acidemia: Metabolic susceptibility and the role of immunosuppressionAlberto B Burlina, Alessandro P Burlina, Renzo Mignani, et al.
International Journal of Colorectal Disease|April 20, 1999
Detection of colonic dysplasia by light-induced fluorescence endoscopy: a pilot studyS Brand, H Stepp, T Ochsenkühn, et al.
Blood|November 15, 1992
Reversible conformational changes induced in glycoprotein IIb-IIIa by a potent and selective peptidomimetic inhibitorW C Kouns, D Kirchhofer, P Hadváry, et al.
Thrombosis Research|January 1, 1995
Thrombomodulin and ristocetincofactor in homocystinuria: a study in two siblingsH W Schienle, R Seitz, P Nawroth, et al.
Biological Psychiatry|September 11, 2012
Increased sensorimotor gating in recreational and dependent cocaine users is modulated by craving and attention-deficit/hyperactivity disorder symptomsKatrin H Preller, Nina Ingold, Lea M Hulka, et al.
JAMA|August 1, 1986
The management of ruptured abdominal aortic aneurysms in rural Colorado. With a historical note on Kit Carson's deathC M Abernathy, R Baumgartner, H G Butler, et al.
The New England Journal of Medicine|April 4, 2008
Gene identification for the cblD defect of vitamin B12 metabolismDavid Coelho, Terttu Suormala, Martin Stucki, et al.
The Journal of Clinical Endocrinology and Metabolism|April 28, 2005
Pyruvate dehydrogenase phosphatase deficiency: identification of the first mutation in two brothers and restoration of activity by protein complementationMary C Maj, Neviana MacKay, Valeriy Levandovskiy, et al.
Pageof 77

Showing results (601-610 of 770) with videos related to

Sort By:
Pageof 77
The International Journal of Neuropsychopharmacology|November 1, 2017
Social Cognition and Interaction in Chronic Users of 3,4-Methylenedioxymethamphetamine (MDMA, "Ecstasy")Michael D Wunderli, Matthias Vonmoos, Lorena Treichler, et al.
European Journal of Pediatrics|March 1, 1990
Methylmalonic aciduria with homocystinuria: biochemical studies, treatment, and clinical course of a Cbl-C patientA Ribes, P Briones, M A Vilaseca, et al.
JIMD Reports|March 6, 2024
Non-Hodgkin lymphoma in a kidney transplanted patient with methylmalonic acidemia: Metabolic susceptibility and the role of immunosuppressionAlberto B Burlina, Alessandro P Burlina, Renzo Mignani, et al.
International Journal of Colorectal Disease|April 20, 1999
Detection of colonic dysplasia by light-induced fluorescence endoscopy: a pilot studyS Brand, H Stepp, T Ochsenkühn, et al.
Blood|November 15, 1992
Reversible conformational changes induced in glycoprotein IIb-IIIa by a potent and selective peptidomimetic inhibitorW C Kouns, D Kirchhofer, P Hadváry, et al.
Thrombosis Research|January 1, 1995
Thrombomodulin and ristocetincofactor in homocystinuria: a study in two siblingsH W Schienle, R Seitz, P Nawroth, et al.
Biological Psychiatry|September 11, 2012
Increased sensorimotor gating in recreational and dependent cocaine users is modulated by craving and attention-deficit/hyperactivity disorder symptomsKatrin H Preller, Nina Ingold, Lea M Hulka, et al.
JAMA|August 1, 1986
The management of ruptured abdominal aortic aneurysms in rural Colorado. With a historical note on Kit Carson's deathC M Abernathy, R Baumgartner, H G Butler, et al.
The New England Journal of Medicine|April 4, 2008
Gene identification for the cblD defect of vitamin B12 metabolismDavid Coelho, Terttu Suormala, Martin Stucki, et al.
The Journal of Clinical Endocrinology and Metabolism|April 28, 2005
Pyruvate dehydrogenase phosphatase deficiency: identification of the first mutation in two brothers and restoration of activity by protein complementationMary C Maj, Neviana MacKay, Valeriy Levandovskiy, et al.
Pageof 77