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F Poggi-Travert

Showing results (1-10 of 11) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1995
Clinical approach to inherited peroxisomal disordersF Poggi-Travert, B Fournier, B T Poll-The, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Protein glycosylation deficiency: clinical presentation]H Ogier de Baulny, F Poggi-Travert, M Besnard, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Therapeutic use of carbamylglutamate in the case of carbamoyl-phosphate synthetase deficiencyG Kuchler, D Rabier, F Poggi-Travert, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Monoamine decarboxylase deficiency]T Billette de Villemeur, P de Lonlay, F Poggi-Travert, et al.
European Journal of Pediatrics|September 4, 1998
Long-term treatment of persistent hyperinsulinaemic hypoglycaemia of infancy with diazoxide: a retrospective review of 77 cases and analysis of efficacy-predicting criteriaG Touati, F Poggi-Travert, H Ogier de Baulny, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 1, 1994
[Diagnosis of metabolic coma in children]F Poggi-Travert, B Héron, T Billette de Villemeur, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Liver transplantation in two cases of propionic acidaemiaJ S Schlenzig, F Poggi-Travert, J Laurent, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Metabolic intermediates in lactic acidosis: compounds, samples and interpretationF Poggi-Travert, D Martin, T Billette de Villemeur, et al.
The New England Journal of Medicine|April 15, 1999
Clinical features of 52 neonates with hyperinsulinismP de Lonlay-Debeney, F Poggi-Travert, J C Fournet, et al.
Journal of Inherited Metabolic Disease|July 17, 1999
Recognition and management of fatty acid oxidation defects: a series of 107 patientsJ M Saudubray, D Martin, P de Lonlay, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Journal of Inherited Metabolic Disease|January 1, 1995
Clinical approach to inherited peroxisomal disordersF Poggi-Travert, B Fournier, B T Poll-The, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Protein glycosylation deficiency: clinical presentation]H Ogier de Baulny, F Poggi-Travert, M Besnard, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Therapeutic use of carbamylglutamate in the case of carbamoyl-phosphate synthetase deficiencyG Kuchler, D Rabier, F Poggi-Travert, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Monoamine decarboxylase deficiency]T Billette de Villemeur, P de Lonlay, F Poggi-Travert, et al.
European Journal of Pediatrics|September 4, 1998
Long-term treatment of persistent hyperinsulinaemic hypoglycaemia of infancy with diazoxide: a retrospective review of 77 cases and analysis of efficacy-predicting criteriaG Touati, F Poggi-Travert, H Ogier de Baulny, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 1, 1994
[Diagnosis of metabolic coma in children]F Poggi-Travert, B Héron, T Billette de Villemeur, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Liver transplantation in two cases of propionic acidaemiaJ S Schlenzig, F Poggi-Travert, J Laurent, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Metabolic intermediates in lactic acidosis: compounds, samples and interpretationF Poggi-Travert, D Martin, T Billette de Villemeur, et al.
The New England Journal of Medicine|April 15, 1999
Clinical features of 52 neonates with hyperinsulinismP de Lonlay-Debeney, F Poggi-Travert, J C Fournet, et al.
Journal of Inherited Metabolic Disease|July 17, 1999
Recognition and management of fatty acid oxidation defects: a series of 107 patientsJ M Saudubray, D Martin, P de Lonlay, et al.
Pageof 2