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Karine Auré

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Caroline Comte; Nina Entelis; Anne-Marie Heckel-Mager; Anne Lombès; Robert P Martin; Alexandre Smirnov; Karine Auré; Abdeldjalil Boucheham; Yann Tonin; Ivan Tarassov
Mitochondrial targeting of recombinant RNAs modulates the level of a heteroplasmic mutation in human mitochondrial DNA associated with Kearns Sayre Syndrome.
Woranontee Weraarpachai; Hana Antonicka; Karine Auré; Anne Lombès; Tamiko Nishimura; Agnès Rötig; Florin Sasarman; Eric A Shoubridge
Mutations in C12orf62, a factor that couples COX I synthesis with cytochrome c oxidase assembly, cause fatal neonatal lactic acidosis.
David Grabli; Karine Auré; Emmanuel Roze
[Movement disorders and neurometabolic diseases].

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All Publications

2013: Caroline Comte; Nina Entelis; Anne-Marie Heckel-Mager; Anne Lombès; Robert P Martin; Alexandre Smirnov; Karine Auré; Abdeldjalil Boucheham; Yann Tonin; Ivan Tarassov
Mitochondrial targeting of recombinant RNAs modulates the level of a heteroplasmic mutation in human mitochondrial DNA associated with Kearns Sayre Syndrome.
Nucleic acids research 2013;41(1):418-33.
2012: Woranontee Weraarpachai; Hana Antonicka; Karine Auré; Anne Lombès; Tamiko Nishimura; Agnès Rötig; Florin Sasarman; Eric A Shoubridge
Mutations in C12orf62, a factor that couples COX I synthesis with cytochrome c oxidase assembly, cause fatal neonatal lactic acidosis.
American journal of human genetics 2012;90(1):142-51.
2011: David Grabli; Karine Auré; Emmanuel Roze
[Movement disorders and neurometabolic diseases].
Revue neurologique 2011;167(2):123-34.
2010: Sabrina Sacconi; Eva Trevisson; Leonardo Salviati; Ségolène Aymé; Odile Rigal; Alberto Garcia Redondo; Michelangelo Mancuso; Gabriele Siciliano; Paola Tonin; Corrado Angelini; Karine Auré; Anne Lombès; Claude Desnuelle
Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy.
Neuromuscular disorders : NMD 2010;20(1):44-8.
2007: Karine Auré; Hélène Ogier de Baulny; Pascal Laforêt; Claude Jardel; Bruno Eymard; Anne Lombès
Chronic progressive ophthalmoplegia with large-scale mtDNA rearrangement: can we predict progression?
Brain : a journal of neurology 2007;130(Pt 6):1516-24.
2007: Karine Auré; Kamel Mamchaoui; Paule Frachon; Gillian Butler-Browne; Anne Lombès; Vincent Mouly
Impact on oxidative phosphorylation of immortalization with the telomerase gene.
Neuromuscular disorders : NMD 2007;17(5):368-75.
2007: Karine Auré; Anne Lombès
[Diagnostic investigations of mitochondrial diseases with neurological symptoms].
Revue neurologique 2007;163(2):254-63.
2007: Florence Malka; Karine Auré; Steffi Goffart; Johannes N Spelbrink; Manuel Rojo
The mitochondria of cultured mammalian cells: I. Analysis by immunofluorescence microscopy, histochemistry, subcellular fractionation, and cell fusion.
Methods in molecular biology (Clifton, N.J.) 2007;372():3-16.
2006: Karine Auré; Florence Laigle-Donadey; Gentian Kaloshi; A Amiel-Benouaich; Marc Sanson
[Multiple gliomas: clinical studies and pathophysiological hypothesis].
Revue neurologique 2006;162(8-9):845-51.
2006: Karine Auré; Guillemette Fayet; Jean-Paul Leroy; Emmanuelle Lacène; Norma B Romero; Anne Lombès
Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
Brain : a journal of neurology 2006;129(Pt 5):1249-59.
2005: Karine Auré; Claude Jardel; Anne Lombès
[Mitochondrial diseases: molecular mechanisms, clinical presentations and diagnosis investigations].
Annales de pathologie 2005;25(4):270-81.
2005: Karine Auré; A Béhin; F Louillet; C Lafitte; Marc Sanson; J P Vernant
Dramatic improvement in non-AIDS related progressive multifocal leucoencephalopathy.
Journal of neurology, neurosurgery, and psychiatry 2005;76(9):1305-6.
2004: Karine Auré; Jean-François Benoist; Hélène Ogier de Baulny; Norma B Romero; Odile Rigal; Anne Lombès
Progression despite replacement of a myopathic form of coenzyme Q10 defect.
Neurology 2004;63(4):727-9.
2003: Karine Auré; Damien Sternberg; Thierry Maisonobe; Serge Herson; Claude Jardel; Patricia Blondy; Anne Lombès; Bruno Eymard; Pascal Laforêt
[Myopathy-lipomatosis associated with A8344G mitochondrial DNA mutation].
Revue neurologique 2003;159(12):1163-8.