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[Epilepsy and mitochondrial diseases: retrospective study on 53 epileptic children]. [electronic resource] by
- Caietta, E
- Cano, A
- Halbert, C
- Hugonenq, C
- Mancini, J
- Milh, M
- Lépine, A
- Villeneuve, N
- Chaussenot, A
- Paquis-Flucklinger, V
- Chabrol, B
Producer: 20130108
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 19
Availability: No items available.
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7.
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Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1-related disorders. [electronic resource] by
- Chaussenot, A
- Rouzier, C
- Quere, M
- Plutino, M
- Ait-El-Mkadem, S
- Bannwarth, S
- Barth, M
- Dollfus, H
- Charles, P
- Nicolino, M
- Chabrol, B
- Vialettes, B
- Paquis-Flucklinger, V
Producer: 20160104
In:
Clinical genetics vol. 87
Availability: No items available.
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8.
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[Sweet heart. Hypertrophic cardiomyopathy in a 49-year-old man]. [electronic resource] by
- Benyamine, A
- Riccardi, F
- Coze, S
- Jacquier, A
- Chaussenot, A
- Paquis, V
- Sallée, M
- Aissi, K
- Thuny, F
- Frances, Y
- Granel, B
- Bauvois, A
- Malezieux-Picard, A
- Mourguet, M
- Murarasu, A
- Saada, N
Producer: 20170421
In:
La Revue de medecine interne vol. 37
Availability: No items available.
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The severity of phenotype linked to SUCLG1 mutations could be correlated with residual amount of SUCLG1 protein. [electronic resource] by
- Rouzier, C
- Le Guédard-Méreuze, S
- Fragaki, K
- Serre, V
- Miro, J
- Tuffery-Giraud, S
- Chaussenot, A
- Bannwarth, S
- Caruba, C
- Ostergaard, E
- Pellissier, J-F
- Richelme, C
- Espil, C
- Chabrol, B
- Paquis-Flucklinger, V
Producer: 20110128
In:
Journal of medical genetics vol. 47
Availability: No items available.
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