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European Journal of Clinical Investigation|February 1, 1994
The diagnosis of pulmonary tuberculosis by gaschromatographic detection of tuberculostearic acid using flame ionisation detectorsA Herz, M Leichsenring, M Felten, et al.The Journal of Pediatrics|February 5, 1999
Treatment of ataxia in isolated vitamin E deficiency caused by alpha-tocopherol transfer protein deficiencyM Schuelke, E Mayatepek, M Inter, et al.Archives of Disease in Childhood|February 24, 2001
Exercise induced hypoglycaemic hyperinsulinismT Meissner, T Otonkoski, R Feneberg, et al.Klinische Padiatrie|November 26, 1999
[Application of indirect calorimetry in monitoring feeding of low birth-weight preterm infants]T Krämer, T Böhler, A R Janecke, et al.Journal of Inherited Metabolic Disease|March 18, 2003
Emergency management of inherited metabolic diseasesV Prietsch, M Lindner, J Zschocke, et al.Early Human Development|May 13, 1999
Increased energy expenditure and fecal fat excretion do not impair weight gain in small-for-gestational-age preterm infantsT Böhler, T Krämer, A R Janecke, et al.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|July 1, 1990
[Pre- and postnatal diagnosis of organoacidopathies]G F Hoffmann, C Jakobs, D Rating, et al.Journal of Inherited Metabolic Disease|June 10, 2006
Neonatal screening for glutaric aciduria type I: strategies to proceedM Lindner, S Ho, J Fang-Hoffmann, et al.Chest|May 16, 2000
Urinary leukotriene E(4) levels are not increased prior to high-altitude pulmonary edemaP Bärtsch, U Eichenberger, P E Ballmer, et al.Journal of Inherited Metabolic Disease|November 8, 2003
Silent and symptomatic primary carnitine deficiency within the same family due to identical mutations in the organic cation/carnitine transporter OCTN2U Spiekerkoetter, G Huener, T Baykal, et al.Pageof 28