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Florence Poggi

Human trifunctional protein deficiency: A new disorder of mitochondrial fatty acid β-oridation
1992 · R.J.A. Wanders, L. Ijlst, et al. · Biochemical and Biophysical Research Communications · 152
Clinical outcome of long-term management of patients with vitamin B12-unresponsive methylmalonic acidemia
1994 · S.B. van der Meer, F. Poggi, et al. · The Journal of Pediatrics · 129
Clinical outcome and long-term management of 17 patients with propionic acidaemia
1996 · S. B. van der Meer, F. Poggi, et al. · European Journal of Pediatrics · 82
Continuous venovenous haemodiafiltration in the acute phase of neonatal maple syrup urine disease
1997 · P. Jouvet, F. Poggi, et al. · Journal of Inherited Metabolic Disease · 55
Human liver pathology in peroxisomal diseases: A review including novel data
1993 · F. Roels, M. Espeel, et al. · Biochimie · 54
Cutaneous manifestations of methylmalonic and propionic acidaemia: a description based on 38 cases
1994 · C. BODEMER, Y. DE PROST, et al. · British Journal of Dermatology · 52
Biochemical and genetic studies of four patients with pyruvate dehydrogenase E1α deficiency
1997 · Cécile Marsac, Chantal Benelli, et al. · Human Genetics · 51
Contribution of odd-chain fatty acid oxidation to propionate production in disorders of propionate metabolism
1994 · D Sbaï, C Narcy, et al. · American Journal of Clinical Nutrition · 43
Aberrant Splicing of Exon 6 in the Pyruvate Denydrogenase-Elα mRNA Linked to a Silent Mutation in a Large Family with Leigh's Encephalomyelopathy
1994 · Linda De Meirleir, Willy Lissens, et al. · Pediatric Research · 39
Peroxisome mosaicism in the livers of peroxisomal deficiency patients
1995 · Marc Espeel, Hanna Mandel, et al. · Hepatology · 35
Defect in the X-Lipoyl-Containing Component of the Pyruvate Dehydrogenase Complex in a Patient With a Neonatal Lactic Acidemia
1996 · V. GEOFFROY, F. FOUQUE, et al. · PEDIATRICS · 27
Retrospective diagnosis of carnitine‐acylcarnitine translocase deficiency by acylcarnitine analysis in the proband Guthrie card and enzymatic studies in the parents
1996 · M. Brivet, A. Slama, et al. · Journal of Inherited Metabolic Disease · 22
Nesidioblastosis and persistent neonatal hyperinsulinism.
1995 · C Sempoux, F Poggi, et al. · PubMed · 21
Immunolocalization of a 43 kDa peroxisomal membrane protein in the liver of patients with generalized peroxisomal disorders.
1995 · M Espeel, F Roels, et al. · PubMed · 21
Definitive cure of hyperammonemia by liver transplantation in urea cycle defects: report of three cases.
1994 · D Jan, F Poggi, et al. · PubMed · 14
Cell and tissue heterogeneity in peroxisomal patients
1995 · Frank Roels, Marc Espeel, et al. · Ghent University Academic Bibliography (Ghent University) · 11
Do criteria exist from urinary organic acids to distinguish β‐oxidation defects?
1995 · D. Rabier, J. Bardet, et al. · Journal of Inherited Metabolic Disease · 9
Hypoglycémie hyperinsulinémique persistante du nouveau-né et du nourrisson
1998 · P de Lonlay-Debeney, JC Fournet, et al. · Archives de Pédiatrie · 7
Liver transplantation: new indications in metabolic disorders?
1994 · D Jan, F Poggi, et al. · PubMed · 7
Liver transplantation in children with inherited metabolic disorders.
1995 · D Jan, J Laurent, et al. · PubMed · 5
[Protocol of metabolic investigations in hereditary metabolic diseases].
1994 · F Poggi, D Rabier, et al. · PubMed · 5
Continuous venovenous haemofiltration in the acute treatment of inborn errors of metabolism
1995 · P. Jouvet, F. Poggi, et al. · Pediatric Nephrology · 4
Cytoplasmic catalase but correct localization of four peroxisomal enzymes in the liver of a child with several peroxisomal dysfunctions
1993 · Marc Espeel, F Poggi, et al. · Ghent University Academic Bibliography (Ghent University) · 1
[Nesidioblastosis and persistent neonatal hyperinsulinism].
1995 · J Rahier, C Sempoux, et al. · PubMed
Mosaicism of hepatic peroxisome distribution in peroxisomal patients
1994 · Marc Espeel, Hannah Mandel, et al. · Ghent University Academic Bibliography (Ghent University)
Works count: 26
Citation count: 846
H-index: 14
I10-index: 16
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