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Current Molecular Medicine|April 13, 2002
Fanconi-Bickel syndrome--a congenital defect of facilitative glucose transportR Santer, B Steinmann, J SchaubMonatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|June 1, 1991
[Brain abnormality within the scope of a VACTERL association]W Nikischin, I Krolikowski, R SanterApplied Optics|March 22, 2008
Radiative transfer model for the computation of radiance and polarization in an ocean-atmosphere system: polarization properties of suspended matter for remote sensingM Chami, R Santer, E DilligeardActa Paediatrica (Oslo, Norway : 1992)|August 1, 1996
Cerebrospinal fluid concentrations of leukotriene B4 in bacterial meningitisR Santer, E Sievers, J SchaubEuropean Journal of Pediatrics|March 27, 1999
Treatment of hyperinsulinaemic hypoglycaemia with nifedipineD Eichmann, M Hufnagel, P Quick, et al.Journal of Inherited Metabolic Disease|May 10, 2002
Tetrahydrobiopterin responsiveness in phenylketonuria. Two new cases and a review of molecular genetic findingsU Lässker, J Zschocke, N Blau, et al.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|July 1, 1993
[Williams-Beuren syndrome in combination with celiac disease]R Pankau, C J Partsch, A Gosch, et al.Annals of Hematology|April 23, 2003
Neutrophil aggregates in a 13-year-old girl: a rare hematological phenomenonA Claviez, H-A Horst, R Santer, et al.Archives of Disease in Childhood|June 27, 2000
Hereditary fructose intolerance and alpha(1) antitrypsin deficiencyG Hillebrand, R Schneppenheim, H D Oldigs, et al.Pediatric Nephrology (Berlin, Germany)|January 17, 2002
Laboratory signs of activated coagulation are common in Henoch-Schönlein purpuraK Brendel-Müller, A Hahn, R Schneppenheim, et al.Pageof 133