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Keywords: Mitochondrial diseases
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Articles
Biosci Rep (2007) 27 (1-3): 5–9.
Published: 13 June 2007
... of the mtDNA-related diseases. © 2007 The Biochemical Society 2007 mtDNA Epidemiology Mitochondrial diseases ORI GI N A L P A PE R Mitochondrial DNA Medicine Salvatore DiMauro Published online: 5 May 2007 The Biochemical Society 2007 Abstract The small, maternally inherited mitochondrial DNA...
Articles
Biosci Rep (2007) 27 (1-3): 23–30.
Published: 13 June 2007
...Massimiliano Filosto; Giuliano Tomelleri; Paola Tonin; Mauro Scarpelli; Gaetano Vattemi; Nicolò Rizzuto; Alessandro Padovani; Alessandro Simonati The term “mitochondrial diseases” (MD) refers to a group of disorders related to respiratory chain dysfunction. Clinical features are usually extremely...
Articles
Biosci Rep (2007) 27 (1-3): 1–3.
Published: 13 June 2007
..., the Department of Neuroscience of the University of Pisa (Italy) has organised a scientific meeting on October 25th, 2006, to discuss recent progress in the field of mitochondriology. © 2007 The Biochemical Society 2007 Mitochondrion mtDNA Mitochondrial diseases ORI GI N A L P A PE R Foreword...
Articles
Biosci Rep (2007) 27 (1-3): 105–112.
Published: 13 June 2007
... of these disorders is ample, making a precise diagnosis difficult. We will report some of the major clinical phenotypes observed in infancy, their underlining molecular features, and will propose an approach to reach a more complete diagnosis. © 2007 The Biochemical Society 2007 mtDNA Mitochondrial diseases...
Articles
Biosci Rep (2007) 27 (1-3): 125–137.
Published: 13 June 2007
... to primary deficiencies of specific compounds, such as carnitine or coenzyme Q10. There is increasing interest in the administration of reactive oxygen species scavengers both in primary mitochondrial diseases and in neurodegenerative diseases directly or indirectly related to mitochondrial dysfunction...
Articles
Biosci Rep (2007) 27 (1-3): 173–184.
Published: 13 June 2007
... features and the genetic bases, and delineate the possible common pathomechanism for both these disorders. © 2007 The Biochemical Society 2007 Mitochondrial diseases Leber's hereditary optic neuropathy Dominant optic atrophy Retinal ganglion cells ORI GI N A L P A PE R Mitochondrial Optic...