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F Poggi

Showing results (11-20 of 24) with videos related to

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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.
Pediatric Research|December 1, 1994
Aberrant splicing of exon 6 in the pyruvate dehydrogenase-E1 alpha mRNA linked to a silent mutation in a large family with Leigh's encephalomyelopathyL De Meirleir, W Lissens, C Benelli, et al.
The Journal of Pediatrics|December 1, 1994
Clinical outcome of long-term management of patients with vitamin B12-unresponsive methylmalonic acidemiaS B van der Meer, F Poggi, M Spada, 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.
European Journal of Cell Biology|August 1, 1995
Immunolocalization of a 43 kDa peroxisomal membrane protein in the liver of patients with generalized peroxisomal disordersM Espeel, F Roels, M Giros, 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.
Hepatology (Baltimore, Md.)|August 1, 1995
Peroxisome mosaicism in the livers of peroxisomal deficiency patientsM Espeel, H Mandel, F Poggi, et al.
Human Genetics|June 1, 1997
Biochemical and genetic studies of four patients with pyruvate dehydrogenase E1 alpha deficiencyC Marsac, C Benelli, I Desguerre, 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.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
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.
Pediatric Research|December 1, 1994
Aberrant splicing of exon 6 in the pyruvate dehydrogenase-E1 alpha mRNA linked to a silent mutation in a large family with Leigh's encephalomyelopathyL De Meirleir, W Lissens, C Benelli, et al.
The Journal of Pediatrics|December 1, 1994
Clinical outcome of long-term management of patients with vitamin B12-unresponsive methylmalonic acidemiaS B van der Meer, F Poggi, M Spada, 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.
European Journal of Cell Biology|August 1, 1995
Immunolocalization of a 43 kDa peroxisomal membrane protein in the liver of patients with generalized peroxisomal disordersM Espeel, F Roels, M Giros, 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.
Hepatology (Baltimore, Md.)|August 1, 1995
Peroxisome mosaicism in the livers of peroxisomal deficiency patientsM Espeel, H Mandel, F Poggi, et al.
Human Genetics|June 1, 1997
Biochemical and genetic studies of four patients with pyruvate dehydrogenase E1 alpha deficiencyC Marsac, C Benelli, I Desguerre, 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.
Pageof 3