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E Holme

Showing results (61-70 of 111) with videos related to

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Journal of Inherited Metabolic Disease|July 10, 1999
NTBC as palliative treatment in chronic tyrosinaemia type IJ Ros, M A Vilaseca, N Lambruschini, et al.
Metabolism: Clinical and Experimental|December 1, 1996
Pivalic acid-induced carnitine deficiency and physical exercise in humansK Abrahamsson, B O Eriksson, E Holme, et al.
Acta Neuropathologica|January 1, 1987
Mitochondrial encephalomyopathy. A variant with heart failure and liver steatosisA Oldfors, M Tulinius, E Holme, et al.
Neuromuscular Disorders : NMD|December 9, 2003
A novel mutation in the mitochondrial tRNA(Phe) gene associated with mitochondrial myopathyA-R Moslemi, C Lindberg, J Toft, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 29, 1997
Tyrosinemia type III: diagnosis and ten-year follow-upR Cerone, E Holme, M C Schiaffino, et al.
Scandinavian Journal of Medicine & Science in Sports|April 30, 1999
The effect of supervised rehabilitation on strength, postural sway, position sense and re-injury risk after acute ankle ligament sprainE Holme, S P Magnusson, K Becher, et al.
Neurology|October 15, 2003
SURF1 gene mutations in three cases with Leigh syndrome and cytochrome c oxidase deficiencyA-R Moslemi, M Tulinius, N Darin, et al.
European Heart Journal|February 20, 2003
Cardiomyopathy in children with mitochondrial disease; clinical course and cardiological findingsD Holmgren, H Wåhlander, B O Eriksson, et al.
Journal of the Neurological Sciences|July 1, 1992
Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibresA Oldfors, N G Larsson, E Holme, et al.
Biochemical Medicine and Metabolic Biology|June 1, 1994
Impaired ketogenesis in carnitine depletion caused by short-term administration of pivalic acid prodrugK Abrahamsson, B O Eriksson, E Holme, et al.
Pageof 12

Showing results (61-70 of 111) with videos related to

Sort By:
Pageof 12
Journal of Inherited Metabolic Disease|July 10, 1999
NTBC as palliative treatment in chronic tyrosinaemia type IJ Ros, M A Vilaseca, N Lambruschini, et al.
Metabolism: Clinical and Experimental|December 1, 1996
Pivalic acid-induced carnitine deficiency and physical exercise in humansK Abrahamsson, B O Eriksson, E Holme, et al.
Acta Neuropathologica|January 1, 1987
Mitochondrial encephalomyopathy. A variant with heart failure and liver steatosisA Oldfors, M Tulinius, E Holme, et al.
Neuromuscular Disorders : NMD|December 9, 2003
A novel mutation in the mitochondrial tRNA(Phe) gene associated with mitochondrial myopathyA-R Moslemi, C Lindberg, J Toft, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 29, 1997
Tyrosinemia type III: diagnosis and ten-year follow-upR Cerone, E Holme, M C Schiaffino, et al.
Scandinavian Journal of Medicine & Science in Sports|April 30, 1999
The effect of supervised rehabilitation on strength, postural sway, position sense and re-injury risk after acute ankle ligament sprainE Holme, S P Magnusson, K Becher, et al.
Neurology|October 15, 2003
SURF1 gene mutations in three cases with Leigh syndrome and cytochrome c oxidase deficiencyA-R Moslemi, M Tulinius, N Darin, et al.
European Heart Journal|February 20, 2003
Cardiomyopathy in children with mitochondrial disease; clinical course and cardiological findingsD Holmgren, H Wåhlander, B O Eriksson, et al.
Journal of the Neurological Sciences|July 1, 1992
Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibresA Oldfors, N G Larsson, E Holme, et al.
Biochemical Medicine and Metabolic Biology|June 1, 1994
Impaired ketogenesis in carnitine depletion caused by short-term administration of pivalic acid prodrugK Abrahamsson, B O Eriksson, E Holme, et al.
Pageof 12