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AJNR Awards, New Junior Editors, and more. Read the latest AJNR updates

Research ArticlePediatric Neuroimaging

MR Findings in Leigh Syndrome with COX Deficiency and SURF-1 Mutations

Laura Farina, Luisa Chiapparini, Graziella Uziel, Marianna Bugiani, Massimo Zeviani and Mario Savoiardo
American Journal of Neuroradiology August 2002, 23 (7) 1095-1100;
Laura Farina
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Luisa Chiapparini
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Graziella Uziel
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Marianna Bugiani
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Massimo Zeviani
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Mario Savoiardo
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American Journal of Neuroradiology: 23 (7)
American Journal of Neuroradiology
Vol. 23, Issue 7
1 Aug 2002
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Cite this article
Laura Farina, Luisa Chiapparini, Graziella Uziel, Marianna Bugiani, Massimo Zeviani, Mario Savoiardo
MR Findings in Leigh Syndrome with COX Deficiency and SURF-1 Mutations
American Journal of Neuroradiology Aug 2002, 23 (7) 1095-1100;

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MR Findings in Leigh Syndrome with COX Deficiency and SURF-1 Mutations
Laura Farina, Luisa Chiapparini, Graziella Uziel, Marianna Bugiani, Massimo Zeviani, Mario Savoiardo
American Journal of Neuroradiology Aug 2002, 23 (7) 1095-1100;
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Cited By...

  • Leigh Syndrome in Drosophila melanogaster: MORPHOLOGICAL AND BIOCHEMICAL CHARACTERIZATION OF Surf1 POST-TRANSCRIPTIONAL SILENCING
  • Bilateral hypertrophic olivary nucleus degeneration on magnetic resonance imaging in children with Leigh and Leigh-like syndrome
  • SURF1 deficiency causes demyelinating Charcot-Marie-Tooth disease
  • A common pattern of brain MRI imaging in mitochondrial diseases with complex I deficiency
  • Post-transcriptional Silencing and Functional Characterization of the Drosophila melanogaster Homolog of Human Surf1
  • Functional and genetic studies demonstrate that mutation in the COX15 gene can cause Leigh syndrome
  • MR Imaging in Human Rabies
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