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F Poggi

Showing results (1-10 of 24) with videos related to

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La Clinica Terapeutica|July 31, 1990
[Ciprofloxacin in the treatment of respiratory infections]F Poggi, F Tognazzi, M Doddi, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Clinical approach to inherited peroxisomal disordersF Poggi-Travert, B Fournier, B T Poll-The, et al.
Diabete & Metabolisme|December 1, 1995
Nesidioblastosis and persistent neonatal hyperinsulinismC Sempoux, F Poggi, F Brunelle, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 1, 1994
[Protocol of metabolic investigations in hereditary metabolic diseases]F Poggi, D Rabier, A Vassault, et al.
Biochimie|January 1, 1993
Human liver pathology in peroxisomal diseases: a review including novel dataF Roels, M Espeel, F Poggi, et al.
The British Journal of Dermatology|July 1, 1994
Cutaneous manifestations of methylmalonic and propionic acidaemia: a description based on 38 casesC Bodemer, Y De Prost, B Bachollet, 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.
Biochemical and Biophysical Research Communications|November 16, 1992
Human trifunctional protein deficiency: a new disorder of mitochondrial fatty acid beta-oxidationR J Wanders, L IJlst, F Poggi, et al.
Histopathology|April 2, 1998
Partial or near-total pancreatectomy for persistent neonatal hyperinsulinaemic hypoglycaemia: the pathologist's roleJ Rahier, C Sempoux, J C Fournet, et al.
Journal of Inherited Metabolic Disease|August 1, 1997
Continuous venovenous haemodiafiltration in the acute phase of neonatal maple syrup urine diseaseP Jouvet, F Poggi, D Rabier, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
La Clinica Terapeutica|July 31, 1990
[Ciprofloxacin in the treatment of respiratory infections]F Poggi, F Tognazzi, M Doddi, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Clinical approach to inherited peroxisomal disordersF Poggi-Travert, B Fournier, B T Poll-The, et al.
Diabete & Metabolisme|December 1, 1995
Nesidioblastosis and persistent neonatal hyperinsulinismC Sempoux, F Poggi, F Brunelle, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 1, 1994
[Protocol of metabolic investigations in hereditary metabolic diseases]F Poggi, D Rabier, A Vassault, et al.
Biochimie|January 1, 1993
Human liver pathology in peroxisomal diseases: a review including novel dataF Roels, M Espeel, F Poggi, et al.
The British Journal of Dermatology|July 1, 1994
Cutaneous manifestations of methylmalonic and propionic acidaemia: a description based on 38 casesC Bodemer, Y De Prost, B Bachollet, 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.
Biochemical and Biophysical Research Communications|November 16, 1992
Human trifunctional protein deficiency: a new disorder of mitochondrial fatty acid beta-oxidationR J Wanders, L IJlst, F Poggi, et al.
Histopathology|April 2, 1998
Partial or near-total pancreatectomy for persistent neonatal hyperinsulinaemic hypoglycaemia: the pathologist's roleJ Rahier, C Sempoux, J C Fournet, et al.
Journal of Inherited Metabolic Disease|August 1, 1997
Continuous venovenous haemodiafiltration in the acute phase of neonatal maple syrup urine diseaseP Jouvet, F Poggi, D Rabier, et al.
Pageof 3