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C Narcy

Showing results (1-10 of 12) with videos related to

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Annales De Pediatrie|December 1, 1987
[Malaise in infants]C Narcy, C Hennion, M Odièvre
Journal of Inherited Metabolic Disease|January 1, 1991
Arginine remains an essential amino acid after liver transplantation in urea cycle enzyme deficienciesD Rabier, C Narcy, J Bardet, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1991
[Dubowitz syndrome]C Bodemer, L Consten, C Narcy, et al.
Archives Francaises De Pediatrie|February 1, 1987
[The association of megaesophagus, Binder's syndrome and dysautonomia: a new neurocristopathy]C Narcy, P Foucaud, G Cargill, et al.
Biology of the Neonate|January 1, 1990
Clinical approach to inherited metabolic disorders in neonatesJ M Saudubray, C Narcy, L Lyonnet, et al.
The American Journal of Clinical Nutrition|June 1, 1994
Contribution of odd-chain fatty acid oxidation to propionate production in disorders of propionate metabolismD Sbaï, C Narcy, G N Thompson, et al.
Archives Francaises De Pediatrie|November 1, 1991
[Hepatic and renal transplantation in the treatment of type I hyperoxaluria]P Jouvet, P Hubert, D Jan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 1, 1994
[Mid-term outcome of 2 cases with maple syrup urine disease: role of liver transplantation in the treatment]J C Netter, G Cossarizza, C Narcy, et al.
Pediatrics|August 1, 1993
Nasogastric drip feeding as the only treatment of neonatal maple syrup urine diseaseR Parini, L P Sereni, D C Bagozzi, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
A new type of chondrodysplasia punctata associated with peroxisomal dysfunctionB T Poll-The, P Maroteaux, C Narcy, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Annales De Pediatrie|December 1, 1987
[Malaise in infants]C Narcy, C Hennion, M Odièvre
Journal of Inherited Metabolic Disease|January 1, 1991
Arginine remains an essential amino acid after liver transplantation in urea cycle enzyme deficienciesD Rabier, C Narcy, J Bardet, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1991
[Dubowitz syndrome]C Bodemer, L Consten, C Narcy, et al.
Archives Francaises De Pediatrie|February 1, 1987
[The association of megaesophagus, Binder's syndrome and dysautonomia: a new neurocristopathy]C Narcy, P Foucaud, G Cargill, et al.
Biology of the Neonate|January 1, 1990
Clinical approach to inherited metabolic disorders in neonatesJ M Saudubray, C Narcy, L Lyonnet, et al.
The American Journal of Clinical Nutrition|June 1, 1994
Contribution of odd-chain fatty acid oxidation to propionate production in disorders of propionate metabolismD Sbaï, C Narcy, G N Thompson, et al.
Archives Francaises De Pediatrie|November 1, 1991
[Hepatic and renal transplantation in the treatment of type I hyperoxaluria]P Jouvet, P Hubert, D Jan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 1, 1994
[Mid-term outcome of 2 cases with maple syrup urine disease: role of liver transplantation in the treatment]J C Netter, G Cossarizza, C Narcy, et al.
Pediatrics|August 1, 1993
Nasogastric drip feeding as the only treatment of neonatal maple syrup urine diseaseR Parini, L P Sereni, D C Bagozzi, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
A new type of chondrodysplasia punctata associated with peroxisomal dysfunctionB T Poll-The, P Maroteaux, C Narcy, et al.
Pageof 2