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W Sperl

Showing results (61-70 of 112) with videos related to

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Klinische Padiatrie|March 1, 1989
[Diagnostic criteria in classical infantile subacute necrotizing encephalomyelopathy (Leigh's disease)]W Sperl, E Rumpl, F Rittinger, et al.
Leukemia|December 17, 2005
Platelet transfusion can mimic somatic mtDNA mutationsD Meierhofer, S Ebner, J A Mayr, et al.
European Journal of Pediatrics|July 1, 1993
Interleukin-3, interleukin-6, granulocyte-macrophage colony-stimulating factor and erythropoietin cord blood levels of preterm and term neonatesB Meister, M Herold, A Mayr, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Continuous arteriovenous haemofiltration in a neonate with hyperammonaemic coma due to citrullinaemiaW Sperl, R Geiger, H Maurer, et al.
Molecular and Cellular Biochemistry|October 6, 1997
High resolution respirometry of permeabilized skeletal muscle fibers in the diagnosis of neuromuscular disordersW Sperl, D Skladal, E Gnaiger, et al.
European Journal of Pediatrics|April 1, 1990
Nephrosis in two siblings with infantile sialic acid storage diseaseW Sperl, W Gruber, J Quatacker, et al.
Annals of the New York Academy of Sciences|February 3, 1999
Galanin and galanin receptor expression in neuroblastomaC Tuechler, R Hametner, N Jones, et al.
European Journal of Pediatrics|February 1, 2000
Odd-numbered long-chain fatty acids in propionic acidaemiaW Sperl, C Murr, D Skladal, et al.
Journal of Inherited Metabolic Disease|July 23, 2003
Hypohomocysteinaemia and highly increased proportion of S-sulfonated plasma transthyretin in molybdenum cofactor deficiencyJ O Sass, M Kishikawa, R Puttinger, et al.
European Journal of Pediatrics|May 1, 1988
Mitochondrial myopathy with lactic acidaemia, Fanconi-De Toni-Debré syndrome and a disturbed succinate: cytochrome c oxidoreductase activityW Sperl, W Ruitenbeek, J M Trijbels, et al.
Pageof 12

Showing results (61-70 of 112) with videos related to

Sort By:
Pageof 12
Klinische Padiatrie|March 1, 1989
[Diagnostic criteria in classical infantile subacute necrotizing encephalomyelopathy (Leigh's disease)]W Sperl, E Rumpl, F Rittinger, et al.
Leukemia|December 17, 2005
Platelet transfusion can mimic somatic mtDNA mutationsD Meierhofer, S Ebner, J A Mayr, et al.
European Journal of Pediatrics|July 1, 1993
Interleukin-3, interleukin-6, granulocyte-macrophage colony-stimulating factor and erythropoietin cord blood levels of preterm and term neonatesB Meister, M Herold, A Mayr, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Continuous arteriovenous haemofiltration in a neonate with hyperammonaemic coma due to citrullinaemiaW Sperl, R Geiger, H Maurer, et al.
Molecular and Cellular Biochemistry|October 6, 1997
High resolution respirometry of permeabilized skeletal muscle fibers in the diagnosis of neuromuscular disordersW Sperl, D Skladal, E Gnaiger, et al.
European Journal of Pediatrics|April 1, 1990
Nephrosis in two siblings with infantile sialic acid storage diseaseW Sperl, W Gruber, J Quatacker, et al.
Annals of the New York Academy of Sciences|February 3, 1999
Galanin and galanin receptor expression in neuroblastomaC Tuechler, R Hametner, N Jones, et al.
European Journal of Pediatrics|February 1, 2000
Odd-numbered long-chain fatty acids in propionic acidaemiaW Sperl, C Murr, D Skladal, et al.
Journal of Inherited Metabolic Disease|July 23, 2003
Hypohomocysteinaemia and highly increased proportion of S-sulfonated plasma transthyretin in molybdenum cofactor deficiencyJ O Sass, M Kishikawa, R Puttinger, et al.
European Journal of Pediatrics|May 1, 1988
Mitochondrial myopathy with lactic acidaemia, Fanconi-De Toni-Debré syndrome and a disturbed succinate: cytochrome c oxidoreductase activityW Sperl, W Ruitenbeek, J M Trijbels, et al.
Pageof 12