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W Sperl

Showing results (51-60 of 112) with videos related to

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Medical Hypotheses|November 24, 1998
The therapeutic potential of oral creatine supplementation in muscle diseaseM Wyss, S Felber, D Skladal, et al.
European Journal of Pediatrics|February 1, 1995
Reversible hepatic veno-occlusive disease in an infant after consumption of pyrrolizidine-containing herbal teaW Sperl, H Stuppner, I Gassner, et al.
Neurological Research|April 14, 2000
Oral creatine supplementation in Duchenne muscular dystrophy: a clinical and 31P magnetic resonance spectroscopy studyS Felber, D Skladal, M Wyss, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|April 23, 2005
Nutritional infantile vitamin B12 deficiency: pathobiochemical considerations in seven patientsB Roschitz, B Plecko, M Huemer, et al.
Journal of Magnetic Resonance Imaging : JMRI|June 22, 2000
Magnetic resonance spectroscopy (MRS) in five patients with treated propionic acidemiaA P Chemelli, M Schocke, W Sperl, et al.
American Journal of Medical Genetics|March 10, 2001
Calvarial "doughnut lesions": clinical spectrum of the syndrome, report on a case, and review of the literatureD Baumgartner, I Gassner, W Sperl, et al.
Clinical Pediatrics|December 8, 2004
Propionic acidemia revisited: a workshop reportJ O Sass, M Hofmann, D Skladal, et al.
British Journal of Cancer|January 13, 2006
Mitochondrial DNA mutations in renal cell carcinomas revealed no general impact on energy metabolismD Meierhofer, J A Mayr, K Fink, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Factor XI and phosphorylase b kinase deficiencyB Sölder, C Pechlaner, W Sperl, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Heterogeneous tissue expression of enzyme defects in mitochondrial myopathiesW Sperl, W Ruitenbeek, J M Trijbels, et al.
Pageof 12

Showing results (51-60 of 112) with videos related to

Sort By:
Pageof 12
Medical Hypotheses|November 24, 1998
The therapeutic potential of oral creatine supplementation in muscle diseaseM Wyss, S Felber, D Skladal, et al.
European Journal of Pediatrics|February 1, 1995
Reversible hepatic veno-occlusive disease in an infant after consumption of pyrrolizidine-containing herbal teaW Sperl, H Stuppner, I Gassner, et al.
Neurological Research|April 14, 2000
Oral creatine supplementation in Duchenne muscular dystrophy: a clinical and 31P magnetic resonance spectroscopy studyS Felber, D Skladal, M Wyss, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|April 23, 2005
Nutritional infantile vitamin B12 deficiency: pathobiochemical considerations in seven patientsB Roschitz, B Plecko, M Huemer, et al.
Journal of Magnetic Resonance Imaging : JMRI|June 22, 2000
Magnetic resonance spectroscopy (MRS) in five patients with treated propionic acidemiaA P Chemelli, M Schocke, W Sperl, et al.
American Journal of Medical Genetics|March 10, 2001
Calvarial "doughnut lesions": clinical spectrum of the syndrome, report on a case, and review of the literatureD Baumgartner, I Gassner, W Sperl, et al.
Clinical Pediatrics|December 8, 2004
Propionic acidemia revisited: a workshop reportJ O Sass, M Hofmann, D Skladal, et al.
British Journal of Cancer|January 13, 2006
Mitochondrial DNA mutations in renal cell carcinomas revealed no general impact on energy metabolismD Meierhofer, J A Mayr, K Fink, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Factor XI and phosphorylase b kinase deficiencyB Sölder, C Pechlaner, W Sperl, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Heterogeneous tissue expression of enzyme defects in mitochondrial myopathiesW Sperl, W Ruitenbeek, J M Trijbels, et al.
Pageof 12