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Journal of Medical Genetics|September 6, 2005
Genetic and clinical aspects of Zellweger spectrum patients with PEX1 mutationsH Rosewich, A Ohlenbusch, J GärtnerJournal of Inherited Metabolic Disease|April 17, 2008
Cerebral MRI as a valuable diagnostic tool in Zellweger spectrum patientsS Weller, H Rosewich, J GärtnerJournal of Inherited Metabolic Disease|August 5, 2016
Diagnostic and prognostic value of in vivo proton MR spectroscopy for Zellweger syndrome spectrum patientsH Rosewich, P Dechent, C Krause, et al.European Journal of Neurology|December 17, 2013
Clinical presentation of pediatric multiple sclerosis before pubertyB Huppke, D Ellenberger, H Rosewich, et al.Neuropediatrics|June 15, 2006
Pitfall in metabolic screening in a patient with fatal peroxisomal beta-oxidation defectH Rosewich, H R Waterham, R J A Wanders, et al.Journal of Lipid Research|January 23, 2010
Rapid quantification of conjugated and unconjugated bile acids and C27 precursors in dried blood spots and small volumes of serumN Janzen, S Sander, M Terhardt, et al.Neuropediatrics|June 10, 2005
Prosaposin deficiency -- a rarely diagnosed, rapidly progressing, neonatal neurovisceral lipid storage disease. Report of a further patientM Elleder, M Jerábková, A Befekadu, et al.Free Radical Biology & Medicine|November 2, 2025
Mitochondrial dysfunction and impaired oxidative stress defense as potential trigger of cerebral X-linked adrenoleukodystrophyL M Marten, M S Lüttgens, B Berečić, et al.Pageof 1