G.P.186
Fayet, G, Aure, K, Lesimple, P, L’Hermitte-Stead, C, Chevalier, C, Magot, A, Houlgatte, R, Pereon, Y, Lombes, A, Savagner, F
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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Journal Article
On/off dropped head syndrome: A severe adverse event after prolonged treatment with MEK inhibitor
Longvert, C., Maisonobe, T., Saiag, P., Auré, K.
Published in European journal of cancer (1990) (01.03.2018)
Published in European journal of cancer (1990) (01.03.2018)
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Journal Article
G.P.189
Péréon, Y, Magot, A, Fayet, G, Mercier, S, Mussini, J.M, Auré, K, Lombès, A, Jardel, C
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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Journal Article
Impact on oxidative phosphorylation of immortalization with the telomerase gene
Auré, K, Mamchaoui, K, Frachon, P, Butler-Browne, G.S, Lombès, A, Mouly, V
Published in Neuromuscular disorders : NMD (01.05.2007)
Published in Neuromuscular disorders : NMD (01.05.2007)
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Journal Article
Les gliomes multiples : étude clinique et hypothèses physiopathologiques
Auré, K., Laigle-Donadey, F., Kaloshi, G., Amiel-Benouaich, A., Sanson, M.
Published in Revue neurologique (2006)
Published in Revue neurologique (2006)
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Journal Article
Dramatic improvement in non-AIDS related progressive multifocal leucoencephalopathy
Auré, K, Béhin, A, Louillet, F, Lafitte, C, Sanson, M, Vernant, J P
Published in Journal of neurology, neurosurgery and psychiatry (01.09.2005)
Published in Journal of neurology, neurosurgery and psychiatry (01.09.2005)
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Journal Article
G.P.186: Gene expression profile of cybrid cells harbouring a mitochondrial DNA mutation in the MT-ATP6 gene reveals new pathogenic pathway
Fayet, G., Aure, K., Lesimple, P., L’Hermitte-Stead, C., Chevalier, C., Magot, A., Houlgatte, R., Pereon, Y., Lombes, A., Savagner, F.
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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Journal Article
Progression despite replacement of a myopathic form of coenzyme Q10 defect
Auré, K, Benoist, J F, Ogier de Baulny, H, Romero, N B, Rigal, O, Lombès, A
Published in Neurology (24.08.2004)
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Published in Neurology (24.08.2004)
Journal Article
Multiple gliomas: clinical studies and pathophysiological hypothesis
Auré, K, Laigle-Donadey, F, Kaloshi, G, Amiel-Benouaich, A, Sanson, M
Published in Revue neurologique (01.09.2006)
Published in Revue neurologique (01.09.2006)
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Journal Article
P.228 - Trifunctional protein beta subunit (HADHB) mutations associated with periodic paralysis phenotype
Remiche, G., Baudin, P., Buon, C., Praline, J., Auré, K., Abramowicz, M., Sternberg, D., Nicole, S.
Published in Neuromuscular disorders : NMD (01.10.2017)
Published in Neuromuscular disorders : NMD (01.10.2017)
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Journal Article
Trifunctional protein beta subunit ( HADHB ) mutations associated with periodic paralysis phenotype
Remiche, G., Baudin, P., Buon, C., Praline, J., Auré, K., Abramowicz, M., Sternberg, D., Nicole, S.
Published in Neuromuscular disorders : NMD (01.10.2017)
Published in Neuromuscular disorders : NMD (01.10.2017)
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Journal Article
G.P.189: Exercise intolerance associated with atypical facial muscle hypertrophy related to mitochondrial tRNA (Pro) gene mutation
Péréon, Y., Magot, A., Fayet, G., Mercier, S., Mussini, J.M., Auré, K., Lombès, A., Jardel, C.
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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Journal Article