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An abnormal exercise test response revealing a respiratory chain complex III deficiency. [electronic resource] by
- Mousson, B
- Collombet, J M
- Dumoulin, R
- Carrier, H
- Flocard, F
- Bouzidi, M
- Godinot, C
- Maire, I
- Mathieu, M
- Quard, S
Producer: 19951026
In:
Acta neurologica Scandinavica vol. 91
Availability: No items available.
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2-Ketoglutarate dehydrogenase deficiency, a rare cause of primary hyperlactataemia: report of a new case. [electronic resource] by
- Guffon, N
- Lopez-Mediavilla, C
- Dumoulin, R
- Mousson, B
- Godinot, C
- Carrier, H
- Collombet, J M
- Divry, P
- Mathieu, M
- Guibaud, P
Producer: 19940303
In:
Journal of inherited metabolic disease vol. 16
Availability: No items available.
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[Value of skin fibroblasts in culture for the diagnosis of mitochondrial cell dysfunction. Apropos of 5 cases with cytochrome c oxidase deficiency]. [electronic resource] by
- Collombet, J M
- Zabot, M T
- Vidailhet, M
- Maire, I
- Echenne, B
- Floquet, J
- Dumoulin, R
- Rimoldi, M
- Mathieu, M
- Mousson, B
Producer: 19931019
In:
Pediatrie vol. 48
Availability: No items available.
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Human cultured myoblasts: a model for the diagnosis of mitochondrial diseases. [electronic resource] by
- Dumoulin, R
- Mandon, G
- Collombet, J M
- Blond, J L
- Carrier, H
- Godinot, C
- Flocard, F
- Villard, J
- Guibaud, P
- Mathieu, M
Producer: 19950817
In:
Journal of inherited metabolic disease vol. 16
Availability: No items available.
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