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W Sperl

Showing results (21-30 of 112) with videos related to

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Padiatrie Und Padologie|January 1, 1988
[Changes in electrolyte and acid-base equilibrium in children with acute urinary tract infections]W Sperl, J P Guggenbichler, T Warter
Lancet (London, England)|December 1, 2001
Treatment of neonatal hyperammonaemiaJ O Sass, W Sperl, C Bachmann
Padiatrie Und Padologie|January 1, 1985
[Glycine encephalopathy: a non-ketotic disorder of glycine catabolism]W Sperl, J Parth, E Rumpl, et al.
Neuropediatrics|August 1, 1997
Metabolic stroke in carbamyl phosphate synthetase deficiencyW Sperl, S Felber, D Skladal, et al.
European Journal of Pediatrics|November 19, 1997
Stridor as the major presenting symptom in riboflavin-responsive multiple acyl-CoA dehydrogenation deficiencyW Sperl, R Geiger, W Lehnert, et al.
Padiatrie Und Padologie|January 1, 1987
[Severe course of osteopathy in Lowe's oculocerebrorenal syndrome]W Sperl, J Parth, I Gassner, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
On the differences between urinary metabolite excretion and odd-numbered fatty acid production in propionic and methylmalonic acidaemiasU Wendel, A Eissler, W Sperl, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Storage material from urine and tissues in the nephropathic phenotype of infantile sialic acid storage diseaseE Paschke, W Gruber, E Ring, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 1, 1997
Pre- and postnatal medical care and risk of sudden infant death syndromeU Kohlendorfer, E Haberlandt, S Kiechl, et al.
Lancet (London, England)|December 5, 1992
Umbilical cord blood progenitor cells for clinical transplantationB Meister, W Sperl, M Tötsch, et al.
Pageof 12

Showing results (21-30 of 112) with videos related to

Sort By:
Pageof 12
Padiatrie Und Padologie|January 1, 1988
[Changes in electrolyte and acid-base equilibrium in children with acute urinary tract infections]W Sperl, J P Guggenbichler, T Warter
Lancet (London, England)|December 1, 2001
Treatment of neonatal hyperammonaemiaJ O Sass, W Sperl, C Bachmann
Padiatrie Und Padologie|January 1, 1985
[Glycine encephalopathy: a non-ketotic disorder of glycine catabolism]W Sperl, J Parth, E Rumpl, et al.
Neuropediatrics|August 1, 1997
Metabolic stroke in carbamyl phosphate synthetase deficiencyW Sperl, S Felber, D Skladal, et al.
European Journal of Pediatrics|November 19, 1997
Stridor as the major presenting symptom in riboflavin-responsive multiple acyl-CoA dehydrogenation deficiencyW Sperl, R Geiger, W Lehnert, et al.
Padiatrie Und Padologie|January 1, 1987
[Severe course of osteopathy in Lowe's oculocerebrorenal syndrome]W Sperl, J Parth, I Gassner, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
On the differences between urinary metabolite excretion and odd-numbered fatty acid production in propionic and methylmalonic acidaemiasU Wendel, A Eissler, W Sperl, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Storage material from urine and tissues in the nephropathic phenotype of infantile sialic acid storage diseaseE Paschke, W Gruber, E Ring, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 1, 1997
Pre- and postnatal medical care and risk of sudden infant death syndromeU Kohlendorfer, E Haberlandt, S Kiechl, et al.
Lancet (London, England)|December 5, 1992
Umbilical cord blood progenitor cells for clinical transplantationB Meister, W Sperl, M Tötsch, et al.
Pageof 12