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Klinische Padiatrie|February 28, 2001
[Hyperthyroidism in early childhood and a very rare variant of glutaric aciduria: coincidence or causal relation?]P Müller, J Buschmann, L Wagner, et al.Journal of Inherited Metabolic Disease|July 31, 2009
Epilepsy and inborn errors of metabolism in childrenN I Wolf, A García-Cazorla, G F HoffmannEuropean Journal of Pediatrics|January 1, 1994
Screening for defects of branched-chain amino acid metabolismK M Gibson, C F Lee, G F HoffmannPediatric Research|April 12, 2000
Maturation-dependent neurotoxicity of 3-hydroxyglutaric and glutaric acids in vitro: a new pathophysiologic approach to glutaryl-CoA dehydrogenase deficiencyS Kölker, B Ahlemeyer, J Krieglstein, et al.Neuropediatrics|June 25, 1998
Cerebrospinal fluid investigations for neurometabolic disordersG F Hoffmann, R A Surtees, R A WeversJournal of Medical Genetics|March 4, 2000
Mutation analysis in glutaric aciduria type IJ Zschocke, E Quak, P Guldberg, et al.Neuropediatrics|April 25, 2000
5-Lipoxygenase inhibition: a new treatment strategy for Sjögren-Larsson syndromeM A Willemsen, J J Rotteveel, P M Steijlen, et al.Clinical Pediatrics|December 8, 2004
Propionic acidemia revisited: a workshop reportJ O Sass, M Hofmann, D Skladal, et al.The British Journal of Dermatology|January 20, 2005
Toxic epidermal necrolysis in a premature infant of 27 weeks' gestational ageK Lohmeier, M Megahed, K W Schulte, et al.Diabetologia|August 10, 1999
Impaired deformability of erythrocytes and neutrophils in children with newly diagnosed insulin-dependent diabetes mellitusO Linderkamp, P Ruef, E P Zilow, et al.Pageof 28