Showing results (11-20 of 172) with videos related to

Sort By:
Pageof 18
Journal of Inherited Metabolic Disease|April 9, 2008
Liver cell transplantation for the treatment of inborn errors of metabolismJ Meyburg, G F Hoffmann
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 4, 2000
Novel splice site mutation of aspartoacylase gene in a Turkish patient with Canavan diseaseP L Rady, J M Penzien, T Vargas, et al.
European Journal of Pediatrics|December 10, 1997
Glutaric aciduria type 1 (glutaryl-CoA-dehydrogenase deficiency): advances and unanswered questions. Report from an international meetingA Superti-Furga, G F Hoffmann
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 21, 2010
Early onset epilepsy and inherited metabolic disorders: diagnosis and managementAsuri N Prasad, G F Hoffmann
Neuropediatrics|January 22, 2003
White matter disease in cerebral organic acid disorders: clinical implications and suggested pathomechanismsS Kölker, E Mayatepek, G F Hoffmann
Croatian Medical Journal|July 27, 2001
Inborn errors of metabolism at the turn of the millenniumI Barić, K Fumić, G F Hoffmann
Journal of Inherited Metabolic Disease|May 4, 2005
Disorders of intermediary metabolism: toxic leukoencephalopathiesF Hörster, R Surtees, G F Hoffmann
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 25, 2000
Analysis of leukotrienes in cerebrospinal fluid of a reference population and patients with inborn errors of metabolism: further evidence for a pathognomonic profile in LTC(4)-synthesis deficiencyE Mayatepek, R Zelezny, G F Hoffmann
Der Nervenarzt|March 31, 1999
[Enzyme defects of the urea cycle in differential acute encephalopathy diagnosis in adulthood. Diagnosis and current therapy concepts]S Schwarz, S Schwab, G F Hoffmann
European Journal of Pediatrics|May 1, 1994
Medium-chain acyl-CoA dehydrogenase deficiency does not correlate with apparent life-threatening events and the sudden infant death syndrome: results from phenylpropionate loading tests and DNA analysisJ M Penzien, G Molz, U N Wiesmann, et al.
Pageof 18