Detection of Mitochondrial Diseases
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9781461378006, 9781461561118
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Multiple mitochondrial tRNALeu[UUR] mutations associated with infantile myopathy

1997 ◽  
pp. 231-236
Author(s):  
S. Zanssen ◽  
M. Molnar ◽  
J. M. Schröder ◽  
G. Buse

Point mutations in the mitochondrial tRNALys gene: Implications for pathogenesis and mechanism

1997 ◽  
pp. 215-219 ◽  
Author(s):  
Judy P. Masucci ◽  
Eric A. Schon ◽  
Michael P. King
Keyword(s):  
Point Mutations

Non-invasive quantitative 31P MRS assay of mitochondrial function in skeletal muscle in situ

1997 ◽  
pp. 17-22
Author(s):  
Jeroen A. L. Jeneson ◽  
Robert W. Wiseman ◽  
Martin J. Kushmerick
Keyword(s):  
Skeletal Muscle ◽  
Mitochondrial Function ◽  
Non Invasive ◽  
31P Mrs

Identification of mitochondrial deficiency using principal component analysis

1997 ◽  
pp. 149-156
Author(s):  
Gilles Durrieu ◽  
Thierry Letellier ◽  
Jaromír Antoch ◽  
Jean-Marc Deshouillers ◽  
Monique Malgat ◽  
...  
Keyword(s):  
Principal Component Analysis ◽  
Principal Component ◽  
Component Analysis

Mitochondrial Complex I defects in aging

1997 ◽  
pp. 329-333
Author(s):  
Giorgio Lenaz ◽  
Carla Bovina ◽  
Cinzia Castelluccio ◽  
Romana Fato ◽  
Gabriella Formiggini ◽  
...  
Keyword(s):  
Complex I ◽  
Mitochondrial Complex I ◽  
Mitochondrial Complex
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