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Hudson memorial lecture. Neonatal management of organic acidurias. Clinical update. [electronic resource] by
- Saudubray, J M
- Ogier, H
- Charpentier, C
- Depondt, E
- Coudé, F X
- Munnich, A
- Mitchell, G
- Rey, F
- Rey, J
- Frézal, J
Producer: 19841109
In:
Journal of inherited metabolic disease vol. 7 Suppl 1
Availability: No items available.
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38.
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Biotin dependent multiple carboxylase deficiency presenting as a congenital lactic acidosis. [electronic resource] by
- Munnich, A
- Saudubray, J M
- Cotisson, A
- Coudĕ, F X
- Ogier, H
- Charpentier, C
- Marsac, C
- Carrĕ, G
- Bourgeay-Causse, M
- Frĕzal, J
Producer: 19820212
In:
European journal of pediatrics vol. 137
Availability: No items available.
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39.
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Congenital lactic acidosis, alpha-ketoglutaric aciduria and variant form of maple syrup urine disease due to a single enzyme defect: dihydrolipoyl dehydrogenase deficiency. [electronic resource] by
- Munnich, A
- Saudubray, J M
- Taylor, J
- Charpentier, C
- Marsac, C
- Rocchiccioli, F
- Amedee-Manesme, O
- Coude, F X
- Frezal, J
- Robinson, B H
Producer: 19821216
In:
Acta paediatrica Scandinavica vol. 71
Availability: No items available.
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40.
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Protective effects of SR 57746A in central and peripheral models of neurodegenerative disorders in rodents and primates. [electronic resource] by
- Fournier, J
- Steinberg, R
- Gauthier, T
- Keane, P E
- Guzzi, U
- Coudé, F X
- Bougault, I
- Maffrand, J P
- Soubrié, P
- Le Fur, G
Producer: 19931123
In:
Neuroscience vol. 55
Availability: No items available.
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