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Pediatric Research
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January 1, 1982
Defective insulin response to intravenous glucose in congenital lactic acidosis
F X Coude, H Ogier, A Munnich, et al.
Lancet (London, England)
|
May 17, 1980
Fatty-acid-responsive alopecia in multiple carboxylase deficiency
A Munnich, J M Saudubray, F X Coude, et al.
The New England Journal of Medicine
|
December 14, 1978
Dichloroacetate as treatment for congenital lactic acidosis
F X Coude, J M Saudubray, F DeMaugre, et al.
Biochimie
|
January 1, 1983
Developmental changes of citrullinogenesis, mitochondrial N-acetylglutamate content and N-acetylglutamate synthetase in fetal and neonatal rats
D Rabier, P Briand, F X Coude, et al.
Archives Francaises De Pediatrie
|
January 1, 1980
[Prognosis of congenital methylmalonic aciduria. Correlations between tolerance to proteins, response to vitamin B12 and enzymatic defect (author's transl)]
J M Saudubray, C Charpentier, F X Coude, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 1, 1987
Results of 1-year growth hormone (GH)-releasing hormone-(1-44) treatment on growth, somatomedin-C, and 24-hour GH secretion in six children with partial GH deficiency
P E Rochiccioli, M T Tauber, F X Coude, et al.
Pediatrics
|
January 1, 1982
Correlation between blood ammonia concentration and organic acid accumulation in isovaleric and propionic acidemia
F X Coude, H Ogier, G Grimber, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1987
A new family affected by the syndrome of hyperornithinaemia, hyperammonaemia and homocitrullinuria
M Rodes, A Ribes, M Pineda, et al.
Archives Francaises De Pediatrie
|
December 1, 1981
[Lysinuric protein intolerance: a severe hyperammonemia secondary to l-arginine deficiency (author's transl)]]
F X Coude, H Ogier, C Charpentier, et al.
Human Genetics
|
January 1, 1981
Neonatal glutaric aciduria type II: an X-linked recessive inherited disorder
F X Coude, H Ogier, C Charpentier, et al.
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Search research articles
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Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
Pediatric Research
|
January 1, 1982
Defective insulin response to intravenous glucose in congenital lactic acidosis
F X Coude, H Ogier, A Munnich, et al.
Lancet (London, England)
|
May 17, 1980
Fatty-acid-responsive alopecia in multiple carboxylase deficiency
A Munnich, J M Saudubray, F X Coude, et al.
The New England Journal of Medicine
|
December 14, 1978
Dichloroacetate as treatment for congenital lactic acidosis
F X Coude, J M Saudubray, F DeMaugre, et al.
Biochimie
|
January 1, 1983
Developmental changes of citrullinogenesis, mitochondrial N-acetylglutamate content and N-acetylglutamate synthetase in fetal and neonatal rats
D Rabier, P Briand, F X Coude, et al.
Archives Francaises De Pediatrie
|
January 1, 1980
[Prognosis of congenital methylmalonic aciduria. Correlations between tolerance to proteins, response to vitamin B12 and enzymatic defect (author's transl)]
J M Saudubray, C Charpentier, F X Coude, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 1, 1987
Results of 1-year growth hormone (GH)-releasing hormone-(1-44) treatment on growth, somatomedin-C, and 24-hour GH secretion in six children with partial GH deficiency
P E Rochiccioli, M T Tauber, F X Coude, et al.
Pediatrics
|
January 1, 1982
Correlation between blood ammonia concentration and organic acid accumulation in isovaleric and propionic acidemia
F X Coude, H Ogier, G Grimber, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1987
A new family affected by the syndrome of hyperornithinaemia, hyperammonaemia and homocitrullinuria
M Rodes, A Ribes, M Pineda, et al.
Archives Francaises De Pediatrie
|
December 1, 1981
[Lysinuric protein intolerance: a severe hyperammonemia secondary to l-arginine deficiency (author's transl)]]
F X Coude, H Ogier, C Charpentier, et al.
Human Genetics
|
January 1, 1981
Neonatal glutaric aciduria type II: an X-linked recessive inherited disorder
F X Coude, H Ogier, C Charpentier, et al.
Page
of 3