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BMC Medical Genetics|July 24, 2020
Severe syndromic ID and skewed X-inactivation in a girl with NAA10 dysfunction and a novel heterozygous de novo NAA10 p.(His16Pro) variant - a case reportIngrid Bader, Nina McTiernan, Christine Darbakk, et al.Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|June 28, 2000
Further evidence that behavioral tests and neuropeptide mRNA and tissue level alterations can differentiate between typical and atypical antipsychotic drugsR Bauer, A Mayr, W Lederer, et al.Mitochondrion|November 12, 2015
Deficiency of respiratory chain complex I in Hashimoto thyroiditisFranz A Zimmermann, Daniel Neureiter, René G Feichtinger, et al.Chemsuschem|March 8, 2024
Effect of Salts on Laccase-Catalyzed Polymerization of LignosulfonateSebastian A Mayr, Harald Rennhofer, Lars Gille, et al.Neuropediatrics|August 26, 2004
Mitochondrial DNA depletion in Alpers syndromeM Tesarova, J A Mayr, L Wenchich, et al.Molecular & Cellular Proteomics : MCP|April 13, 2013
Protein sets define disease states and predict in vivo effects of drug treatmentDavid Meierhofer, Christopher Weidner, Ludger Hartmann, et al.Journal of Internal Medicine|July 8, 2000
Acute respiratory failure associated with catastrophic antiphospholipid syndromeF J Wiedermann, A Mayr, W Schobersberger, et al.Molecular Genetics and Metabolism|July 21, 2009
A novel mutation of the RRM2B gene in an infant with early fatal encephalomyopathy, central hypomyelination, and tubulopathyBirgit Acham-Roschitz, Barbara Plecko, Franz Lindbichler, et al.Molecular Genetics and Metabolism|December 3, 2025
Lysinuric protein intolerance: Allogeneic peripheral blood stem cell transplantation for an inborn error of metabolism and immunityNatalia Zubarovskaya, Johannes A Mayr, Elmar Aigner, et al.The Laryngoscope|February 21, 2022
Mitochondrial Disease and Hearing Loss in Children: A Systematic ReviewSebastian Roesch, Anna O'Sullivan, Georg Zimmermann, et al.Pageof 56