Showing results (1-10 of 39) with videos related to
Sort By:
Pageof 4
Journal of Biomedicine & Biotechnology|April 17, 2010
Mitochondrial translation and beyond: processes implicated in combined oxidative phosphorylation deficienciesPaulien Smits, Jan Smeitink, Lambert van den HeuvelHuman Genetics|April 6, 2002
CIA30 complex I assembly factor: a candidate for human complex I deficiency?Rolf Janssen, Jan Smeitink, Roel Smeets, et al.Drug Discovery Today|February 19, 2013
Cysteamine: an old drug with new potentialMartine Besouw, Rosalinde Masereeuw, Lambert van den Heuvel, et al.Pediatric Transplantation|December 27, 2023
A longitudinal study of long-term renal outcome after pediatric liver transplantation in relation to CNI exposureSimon Vandewiele, Jean Herman, Lambert van den Heuvel, et al.Current Opinion in Neurology|March 17, 2004
Complex I assembly: a puzzling problemRutger Vogel, Leo Nijtmans, Cristina Ugalde, et al.Molecular Genetics and Metabolism|April 11, 2024
Plasma chitotriosidase enzyme activity as a novel therapeutic monitor for cysteamine treatment in nephropathic cystinosis: A retrospective validation studyKoenraad Veys, Mohamed A Elmonem, Lambert van den Heuvel, et al.Mitochondrion|May 23, 2006
Females with PDHA1 gene mutations: a diagnostic challengeMarjolein Willemsen, Richard J T Rodenburg, Alexandra Teszas, et al.Journal of Inherited Metabolic Disease|March 5, 2015
Whole exome sequencing of suspected mitochondrial patients in clinical practiceSaskia B Wortmann, David A Koolen, Jan A Smeitink, et al.Pediatric Nephrology (Berlin, Germany)|June 7, 2012
Novel C3 mutation p.Lys65Gln in aHUS affects complement factor H bindingElena Volokhina, Dineke Westra, Xiaoguang Xue, et al.European Journal of Pediatrics|January 23, 2017
Occurrence of atypical HUS associated with influenza BKaren van Hoeve, Corinne Vandermeulen, Marc Van Ranst, et al.Pageof 4