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Author/Creator Eymard, B

1. Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolution. Issue 12 (22nd December 2014)

Authors:
Deconinck, N; Richard, P; Allamand, V; Behin, A; Lafôret, P; Ferreiro, A; de Becdelievre, A; Ledeuil, C; Gartioux, C; Nelson, I; Carlier, R Y; Carlier, P; Wahbi, K; Romero, N; Zabot, M T; Bouhour, F; Tiffreau, V; Lacour, A; Eymard, B; Stojkovic, T
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 86:Issue 12(2015)
Page Start:
1337
Record Type:
Journal Article
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4. Novel ϵ subunit mutation of the muscle acetylcholine receptor causing a slow-channel congenital myasthenic syndrome. Issue 4 (16th March 2009)

Authors:
Outteryck, O; Richard, P; Lacour, A; Fournier, E; Zéphir, H; Gaudon, K; Eymard, B; Hantaï, D; Vermersch, P; Stojkovic, T
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 80:Issue 4(2009)
Page Start:
450
Record Type:
Journal Article
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6. Possible founder effect of rapsyn N88K mutation and identification of novel rapsyn mutations in congenital myasthenic syndromes. Issue 6 (1st June 2003)

Authors:
Richard, P; Gaudon, K; Andreux, F; Yasaki, E; Prioleau, C; Bauché, S; Barois, A; Ioos, C; Mayer, M; Routon, M C; Mokhtari, M; Leroy, J P; Fournier, E; Hainque, B; Koenig, J; Fardeau, M; Eymard, B; Hantaï, D
Journal:
Journal of medical genetics
Issue:
Volume 40:Issue 6(2003)
Page Start:
e81
Record Type:
Journal Article
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8. Late-onset cervicoscapular muscle atrophy and weakness after radiotherapy for Hodgkin disease: a case series. Issue 1 (17th December 2009)

Authors:
Furby, A; Béhin, A; Lefaucheur, J-P; Beauvais, K; Marcorelles, P; Mussini, J-M; Bassez, G; Créange, A; Eymard, B; Pénisson-Besnier, I
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 81:Issue 1(2010)
Page Start:
101
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗