F. Poggi-Travert

Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy.

C. Junien, F. Brunelle, J. Saudubray, 1997, The Journal of clinical investigation.

Metabolic intermediates in lactic acidosis: compounds, samples and interpretation

A. Munnich, D. Rabier, P. Kamoun, 1996, Journal of Inherited Metabolic Disease.

Liver transplantation in two cases of propionic acidaemia

Y. Révillon, A. Sewell, D. Rabier, 1995, Journal of Inherited Metabolic Disease.

Recognition and management of fatty acid oxidation defects: A series of 107 patients

D. Rabier, P. Kamoun, J. Saudubray, 1999, Journal of Inherited Metabolic Disease.

Clinical features of 52 neonates with hyperinsulinism.

C. Junien, C. Sempoux, F. Brunelle, 1999, The New England journal of medicine.

Therapeutic use of carbamylglutamate in the case of carbamoyl-phosphate synthetase deficiency

D. Rabier, J. Saudubray, F. Poggi-Travert, 1996, Journal of Inherited Metabolic Disease.

Clinical approach to inherited peroxisomal disorders

B. Poll-The, J. Saudubray, F. Poggi-Travert, 1995, Journal of Inherited Metabolic Disease.

Long-term treatment of persistent hyperinsulinaemic hypoglycaemia of infancy with diazoxide: a retrospective review of 77 cases and analysis of efficacy-predicting criteria

P. Czernichow, F. Brunelle, J. Saudubray, 1998, European Journal of Pediatrics.