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Bone Marrow Transplantation|August 11, 2001
Successful HLA-identical bone marrow transplantation in a patient with PNP deficiency using busulfan and fludarabine for conditioningC F Classen, A S Schulz, M Sigl-Kraetzig, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|November 1, 1991
[Macrocephaly as the initial manifestation of glutaryl-CoA-dehydrogenase deficiency (glutaric aciduria type I)]F K Trefz, G F Hoffmann, E Mayatepek, et al.
Journal of Inherited Metabolic Disease|September 13, 2014
Understanding cerebral L-lysine metabolism: the role of L-pipecolate metabolism in Gcdh-deficient mice as a model for glutaric aciduria type IRoland Posset, Silvana Opp, Eduard A Struys, et al.
European Journal of Pediatrics|March 16, 2022
Sudden neonatal death in individuals with medium-chain acyl-coenzyme A dehydrogenase deficiency: limit of newborn screeningUlrike Mütze, Uta Nennstiel, Birgit Odenwald, et al.
International Journal of Environmental Research and Public Health|March 6, 2021
Maternal Food and Beverage Consumption Behaviors and Discrepant Phthalate Exposure by RaceMary E Sterrett, Michael S Bloom, Erica L Jamro, et al.
The Journal of Organic Chemistry|November 26, 2024
Brønsted Acid-Catalyzed, Asymmetric Allenoate Claisen ReactionRachael E Hamilton, Ellen A Berkley, Iain K Laufer, et al.
The Journal of Clinical Psychiatry|August 17, 2016
Effects of Restricted Time in Bed on Antidepressant Treatment Response: A Randomized Controlled TrialJ Todd Arnedt, Leslie M Swanson, Richard R Dopp, et al.
Neuropediatrics|June 15, 2006
The first case of 3-methylcrotonyl-CoA carboxylase (MCC) deficiency responsive to biotinD Friebel, M von der Hagen, E R Baumgartner, et al.
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