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P Parvy

Showing results (51-60 of 64) with videos related to

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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.
Pediatrics|January 1, 1982
Correlation between blood ammonia concentration and organic acid accumulation in isovaleric and propionic acidemiaF X Coude, H Ogier, G Grimber, et al.
Annales De Genetique|January 1, 1990
[Cri-du-chat disease: plasma and urinary amino acids]J Lejeune, M O Rethoré, M Peeters, et al.
The Journal of Pediatrics|May 1, 1983
Diet-responsive proconvertin (factor VII) deficiency in homocystinuriaA Munnich, J M Saudubray, M D Dautzenberg, et al.
Prenatal Diagnosis|July 1, 1996
Gestational age-related reference values for amniotic fluid amino acids: a useful tool for prenatal diagnosis of aminoacidopathiesD Rabier, B Chadefaux-Vekemans, J F Oury, et al.
The Journal of Pediatrics|August 1, 1994
Recurrent episodes of bizarre behavior in a boy with ornithine transcarbamylase deficiency: diagnostic failure of protein loading and allopurinol challenge testsM Spada, O Guardamagna, D Rabier, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Clinical aspects of mitochondrial disordersA Munnich, P Rustin, A Rötig, et al.
Developmental Biology|June 7, 2005
A role for betaFTZ-F1 in regulating ecdysteroid titers during post-embryonic development in Drosophila melanogasterJ-P Parvy, C Blais, F Bernard, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Abnormal alpha-aminoadipic acid excretion in a newborn with a defect in platelet aggregation and antenatal cerebral haemorrhageM Candito, C Richelme, P Parvy, et al.
The Journal of Pediatrics|December 1, 1991
Hepatic failure in disorders of oxidative phosphorylation with neonatal onsetV Cormier, P Rustin, J P Bonnefont, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
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.
Pediatrics|January 1, 1982
Correlation between blood ammonia concentration and organic acid accumulation in isovaleric and propionic acidemiaF X Coude, H Ogier, G Grimber, et al.
Annales De Genetique|January 1, 1990
[Cri-du-chat disease: plasma and urinary amino acids]J Lejeune, M O Rethoré, M Peeters, et al.
The Journal of Pediatrics|May 1, 1983
Diet-responsive proconvertin (factor VII) deficiency in homocystinuriaA Munnich, J M Saudubray, M D Dautzenberg, et al.
Prenatal Diagnosis|July 1, 1996
Gestational age-related reference values for amniotic fluid amino acids: a useful tool for prenatal diagnosis of aminoacidopathiesD Rabier, B Chadefaux-Vekemans, J F Oury, et al.
The Journal of Pediatrics|August 1, 1994
Recurrent episodes of bizarre behavior in a boy with ornithine transcarbamylase deficiency: diagnostic failure of protein loading and allopurinol challenge testsM Spada, O Guardamagna, D Rabier, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Clinical aspects of mitochondrial disordersA Munnich, P Rustin, A Rötig, et al.
Developmental Biology|June 7, 2005
A role for betaFTZ-F1 in regulating ecdysteroid titers during post-embryonic development in Drosophila melanogasterJ-P Parvy, C Blais, F Bernard, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Abnormal alpha-aminoadipic acid excretion in a newborn with a defect in platelet aggregation and antenatal cerebral haemorrhageM Candito, C Richelme, P Parvy, et al.
The Journal of Pediatrics|December 1, 1991
Hepatic failure in disorders of oxidative phosphorylation with neonatal onsetV Cormier, P Rustin, J P Bonnefont, et al.
Pageof 7