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Journal of Inherited Metabolic Disease
|
July 10, 1999
NTBC as palliative treatment in chronic tyrosinaemia type I
J Ros, M A Vilaseca, N Lambruschini, et al.
Metabolism: Clinical and Experimental
|
December 1, 1996
Pivalic acid-induced carnitine deficiency and physical exercise in humans
K Abrahamsson, B O Eriksson, E Holme, et al.
Acta Neuropathologica
|
January 1, 1987
Mitochondrial encephalomyopathy. A variant with heart failure and liver steatosis
A 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 myopathy
A-R Moslemi, C Lindberg, J Toft, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
October 29, 1997
Tyrosinemia type III: diagnosis and ten-year follow-up
R 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 sprain
E 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 deficiency
A-R Moslemi, M Tulinius, N Darin, et al.
European Heart Journal
|
February 20, 2003
Cardiomyopathy in children with mitochondrial disease; clinical course and cardiological findings
D 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 fibres
A 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 prodrug
K Abrahamsson, B O Eriksson, E Holme, et al.
Page
of 12
Search research articles
Search
Showing results (61-70 of 111) with videos related to
Sort By:
Page
of 12
Journal of Inherited Metabolic Disease
|
July 10, 1999
NTBC as palliative treatment in chronic tyrosinaemia type I
J Ros, M A Vilaseca, N Lambruschini, et al.
Metabolism: Clinical and Experimental
|
December 1, 1996
Pivalic acid-induced carnitine deficiency and physical exercise in humans
K Abrahamsson, B O Eriksson, E Holme, et al.
Acta Neuropathologica
|
January 1, 1987
Mitochondrial encephalomyopathy. A variant with heart failure and liver steatosis
A 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 myopathy
A-R Moslemi, C Lindberg, J Toft, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
October 29, 1997
Tyrosinemia type III: diagnosis and ten-year follow-up
R 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 sprain
E 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 deficiency
A-R Moslemi, M Tulinius, N Darin, et al.
European Heart Journal
|
February 20, 2003
Cardiomyopathy in children with mitochondrial disease; clinical course and cardiological findings
D 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 fibres
A 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 prodrug
K Abrahamsson, B O Eriksson, E Holme, et al.
Page
of 12