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European Journal of Pediatrics
|
April 1, 1993
Carnitine palmitoyl transferase I deficiency presenting as a Reye-like syndrome without hypoglycaemia
C 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 deficiency
B 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 case
N 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.
Page
of 2
Search research articles
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Showing results (11-20 of 14) with videos related to
Sort By:
Page
of 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 hypoglycaemia
C 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 deficiency
B 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 case
N 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.
Page
of 2