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Revue Neurologique
|
January 1, 1986
[A case of myopathy with carnitine deficiency]
P Martin, H Carrier, J F Renaud, et al.
La Nouvelle Presse Medicale
|
September 25, 1982
[Recurrent paroxysmal myoglobinuria with acute renal insufficiency caused by muscular carnitine (palmitoyltransferase deficiency. A case]
J Meunier, D Perrot, M Bret, et al.
Neuromuscular Disorders : NMD
|
September 1, 1993
Decreased expression of ubiquinol-cytochrome c reductase subunits in patients exhibiting mitochondrial myopathy with progressive exercise intolerance
M F Bouzidi, H Schägger, J M Collombet, et al.
Archives Francaises De Pediatrie
|
December 1, 1975
[Clinical, ultrastructural and biochemical study of a case of GM1 type 2 gangliosidosis]
J C Mammelle, M T Vanier, G Baraton, 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 ophthalmoplegia
T Ville-Ferlin, R Dumoulin, G Stepien, et al.
Biochimica Et Biophysica Acta
|
June 7, 1996
Variations of muscle mitochondrial creatine kinase activity in mitochondrial diseases
M F Bouzidi, N Enjolras, H Carrier, 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.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Human cultured myoblasts: a model for the diagnosis of mitochondrial diseases
R Dumoulin, G Mandon, J M Collombet, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 59) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 59 results.
Revue Neurologique
|
January 1, 1986
[A case of myopathy with carnitine deficiency]
P Martin, H Carrier, J F Renaud, et al.
La Nouvelle Presse Medicale
|
September 25, 1982
[Recurrent paroxysmal myoglobinuria with acute renal insufficiency caused by muscular carnitine (palmitoyltransferase deficiency. A case]
J Meunier, D Perrot, M Bret, et al.
Neuromuscular Disorders : NMD
|
September 1, 1993
Decreased expression of ubiquinol-cytochrome c reductase subunits in patients exhibiting mitochondrial myopathy with progressive exercise intolerance
M F Bouzidi, H Schägger, J M Collombet, et al.
Archives Francaises De Pediatrie
|
December 1, 1975
[Clinical, ultrastructural and biochemical study of a case of GM1 type 2 gangliosidosis]
J C Mammelle, M T Vanier, G Baraton, 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 ophthalmoplegia
T Ville-Ferlin, R Dumoulin, G Stepien, et al.
Biochimica Et Biophysica Acta
|
June 7, 1996
Variations of muscle mitochondrial creatine kinase activity in mitochondrial diseases
M F Bouzidi, N Enjolras, H Carrier, 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.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Human cultured myoblasts: a model for the diagnosis of mitochondrial diseases
R Dumoulin, G Mandon, J M Collombet, et al.
Page
of 6