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Sleep Medicine|January 17, 2009
Childhood narcolepsy with partial facial cataplexy: a diagnostic dilemmaKarlien Dhondt, Helene Verhelst, Dirk Pevernagie, et al.Pediatrics|August 14, 2013
Hypocretin-1 deficiency in a girl with ROHHAD syndromeKarlien Dhondt, Patrick Verloo, Hélène Verhelst, et al.Electrophoresis|September 5, 2002
Mass spectrometric identification of mitochondrial oxidative phosphorylation subunits separated by two-dimensional blue-native polyacrylamide gel electrophoresisBart Devreese, Frank Vanrobaeys, Joél Smet, et al.Plos One|September 9, 2022
Urine lactate concentration as a non-invasive screener for metabolic abnormalities: Findings in children with autism spectrum disorder and regressionSofie Boterberg, Elise Vantroys, Boel De Paepe, et al.The American Journal of Forensic Medicine and Pathology|April 16, 2002
An inherited metabolic disorder presenting as ethylene glycol intoxication in a young adultKaren Pien, Bruno van Vlem, Rudy van Coster, et al.Journal of Proteome Research|December 13, 2005
Profiling of myelin proteins by 2D-gel electrophoresis and multidimensional liquid chromatography coupled to MALDI TOF-TOF mass spectrometryFrank Vanrobaeys, Rudy Van Coster, Goedele Dhondt, et al.Journal of Child Psychology and Psychiatry, and Allied Disciplines|May 23, 2006
Event rate and event-related potentials in ADHDRoeljan Wiersema, Jaap van der Meere, Herbert Roeyers, et al.Analytica Chimica Acta|August 29, 2007
Gas chromatographic-mass spectrometric analysis of N-acetylated amino acids: the first case of aminoacylase I deficiencyErik Gerlo, Rudy Van Coster, Willy Lissens, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 8, 2016
Multiple sclerosis in Belgian children: A multicentre retrospective studyHelene Verhelst, Liesbeth De Waele, Nicolas Deconinck, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 9, 2012
X-linked sideroblastic anemia and ataxia: a new family with identification of a fourth ABCB7 gene mutationMarc D'Hooghe, Dominik Selleslag, Geert Mortier, et al.Pageof 13