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W Sperl

Showing results (71-80 of 112) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1994
A family with visceral course of Niemann-Pick disease, macular halo syndrome and low sphingomyelin degradation rateW Sperl, G Bart, M T Vanier, et al.
Epilepsia|August 8, 2001
A case of Ohtahara syndrome with olivary-dentate dysplasia and agenesis of mamillary bodiesE Trinka, C Rauscher, M Nagler, et al.
Journal of Clinical Microbiology|January 16, 1999
Gram type-specific broad-range PCR amplification for rapid detection of 62 pathogenic bacteriaA Klausegger, M Hell, A Berger, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Polarographic studies of saponin-skinned muscle fibres in patients with mitochondrial myopathiesW Sperl, D Skladal, N Lanznaster, et al.
European Journal of Pediatrics|July 1, 1995
Fulminant hepatic failure in a child as a potential adverse effect of trimethoprim-sulphamethoxazoleB Simma, B Meister, J Deutsch, et al.
Neuropediatrics|August 26, 2004
Mitochondrial DNA depletion in Alpers syndromeM Tesarova, J A Mayr, L Wenchich, et al.
Padiatrie Und Padologie|January 1, 1991
[Effects of health and medical undertreatment on the clinical status and social behavior of infants and small children in a Romanian orphanage]D Zaknun, H P Oswald, J Zaknun, et al.
Annals of Clinical Biochemistry|May 1, 1992
Maturation of mitochondrial and other isoenzymes of creatine kinase in skeletal muscle of preterm born infantsJ Smeitink, W Ruitenbeek, T van Lith, et al.
Clinical Pediatrics|November 7, 2003
The clinical spectrum of mitochondrial disease in 75 pediatric patientsD Skladal, C Sudmeier, V Konstantopoulou, et al.
Pediatric Research|December 1, 1992
Atypical (mild) forms of dihydropteridine reductase deficiency: neurochemical evaluation and mutation detectionN Blau, C W Heizmann, W Sperl, et al.
Pageof 12

Showing results (71-80 of 112) with videos related to

Sort By:
Pageof 12
Journal of Inherited Metabolic Disease|January 1, 1994
A family with visceral course of Niemann-Pick disease, macular halo syndrome and low sphingomyelin degradation rateW Sperl, G Bart, M T Vanier, et al.
Epilepsia|August 8, 2001
A case of Ohtahara syndrome with olivary-dentate dysplasia and agenesis of mamillary bodiesE Trinka, C Rauscher, M Nagler, et al.
Journal of Clinical Microbiology|January 16, 1999
Gram type-specific broad-range PCR amplification for rapid detection of 62 pathogenic bacteriaA Klausegger, M Hell, A Berger, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Polarographic studies of saponin-skinned muscle fibres in patients with mitochondrial myopathiesW Sperl, D Skladal, N Lanznaster, et al.
European Journal of Pediatrics|July 1, 1995
Fulminant hepatic failure in a child as a potential adverse effect of trimethoprim-sulphamethoxazoleB Simma, B Meister, J Deutsch, et al.
Neuropediatrics|August 26, 2004
Mitochondrial DNA depletion in Alpers syndromeM Tesarova, J A Mayr, L Wenchich, et al.
Padiatrie Und Padologie|January 1, 1991
[Effects of health and medical undertreatment on the clinical status and social behavior of infants and small children in a Romanian orphanage]D Zaknun, H P Oswald, J Zaknun, et al.
Annals of Clinical Biochemistry|May 1, 1992
Maturation of mitochondrial and other isoenzymes of creatine kinase in skeletal muscle of preterm born infantsJ Smeitink, W Ruitenbeek, T van Lith, et al.
Clinical Pediatrics|November 7, 2003
The clinical spectrum of mitochondrial disease in 75 pediatric patientsD Skladal, C Sudmeier, V Konstantopoulou, et al.
Pediatric Research|December 1, 1992
Atypical (mild) forms of dihydropteridine reductase deficiency: neurochemical evaluation and mutation detectionN Blau, C W Heizmann, W Sperl, et al.
Pageof 12