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R Dumoulin

Showing results (11-20 of 14) with videos related to

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European Journal of Pediatrics|April 1, 1993
Carnitine palmitoyl transferase I deficiency presenting as a Reye-like syndrome without hypoglycaemiaC Vianey-Saban, B Mousson, C Bertrand, et al.
Acta Neurologica Scandinavica|June 1, 1995
An abnormal exercise test response revealing a respiratory chain complex III deficiencyB Mousson, J M Collombet, R Dumoulin, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
2-Ketoglutarate dehydrogenase deficiency, a rare cause of primary hyperlactataemia: report of a new caseN Guffon, C Lopez-Mediavilla, R Dumoulin, et al.
Pediatrie|January 1, 1993
[Value of skin fibroblasts in culture for the diagnosis of mitochondrial cell dysfunction. Apropos of 5 cases with cytochrome c oxidase deficiency]J M Collombet, M T Zabot, M Vidailhet, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
European Journal of Pediatrics|April 1, 1993
Carnitine palmitoyl transferase I deficiency presenting as a Reye-like syndrome without hypoglycaemiaC Vianey-Saban, B Mousson, C Bertrand, et al.
Acta Neurologica Scandinavica|June 1, 1995
An abnormal exercise test response revealing a respiratory chain complex III deficiencyB Mousson, J M Collombet, R Dumoulin, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
2-Ketoglutarate dehydrogenase deficiency, a rare cause of primary hyperlactataemia: report of a new caseN Guffon, C Lopez-Mediavilla, R Dumoulin, et al.
Pediatrie|January 1, 1993
[Value of skin fibroblasts in culture for the diagnosis of mitochondrial cell dysfunction. Apropos of 5 cases with cytochrome c oxidase deficiency]J M Collombet, M T Zabot, M Vidailhet, et al.
Pageof 2