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B Mousson

Showing results (31-40 of 48) with videos related to

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Neuromuscular Disorders : NMD|September 1, 1993
Decreased expression of ubiquinol-cytochrome c reductase subunits in patients exhibiting mitochondrial myopathy with progressive exercise intoleranceM F Bouzidi, H Schägger, J M Collombet, et al.
Molecular and Cellular Probes|June 1, 1995
Fine mapping of randomly distributed multiple deletions of mitochondrial DNA in a case of chronic progressive external ophthalmoplegiaT Ville-Ferlin, R Dumoulin, G Stepien, et al.
La Revue De Medecine Interne|December 31, 2002
[Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (Melas) associated with a Fahr disease and cerebellar calcifications]S Younes-Mhenni, S Thobois, N Streichenberger, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Infantile form of carnitine palmitoyltransferase II deficiency in a girl with rapid fatal onsetC Vianey-Saban, N Stremler, O Paut, et al.
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.
Pediatric Research|November 1, 1994
Rate-dependent distal renal tubular acidosis and carnitine palmitoyltransferase I deficiencyA J Bergman, R A Donckerwolcke, M Duran, 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.
Annales De Biologie Clinique|January 1, 1989
[A recommended method for determination of uric acid in serum]P Baltassat, D Brault, M Cambillau, et al.
Annales De Biologie Clinique|January 1, 1991
[Update of a selected technique for uric acid determination in plasma and serum. Experimental study and value of derivative spectrophotometry]P Baltassat, D Brault, M Cambillau, 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.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Neuromuscular Disorders : NMD|September 1, 1993
Decreased expression of ubiquinol-cytochrome c reductase subunits in patients exhibiting mitochondrial myopathy with progressive exercise intoleranceM F Bouzidi, H Schägger, J M Collombet, et al.
Molecular and Cellular Probes|June 1, 1995
Fine mapping of randomly distributed multiple deletions of mitochondrial DNA in a case of chronic progressive external ophthalmoplegiaT Ville-Ferlin, R Dumoulin, G Stepien, et al.
La Revue De Medecine Interne|December 31, 2002
[Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (Melas) associated with a Fahr disease and cerebellar calcifications]S Younes-Mhenni, S Thobois, N Streichenberger, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Infantile form of carnitine palmitoyltransferase II deficiency in a girl with rapid fatal onsetC Vianey-Saban, N Stremler, O Paut, et al.
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.
Pediatric Research|November 1, 1994
Rate-dependent distal renal tubular acidosis and carnitine palmitoyltransferase I deficiencyA J Bergman, R A Donckerwolcke, M Duran, 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.
Annales De Biologie Clinique|January 1, 1989
[A recommended method for determination of uric acid in serum]P Baltassat, D Brault, M Cambillau, et al.
Annales De Biologie Clinique|January 1, 1991
[Update of a selected technique for uric acid determination in plasma and serum. Experimental study and value of derivative spectrophotometry]P Baltassat, D Brault, M Cambillau, 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.
Pageof 5