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Displaying 17 results.
    • Journal article
    Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11.
    Fournet, J C Mayaud, C de Lonlay, P Gross-Morand, M S Verkarre, V Castanet, M Devillers, Martine[UCL] Rahier, Jacques[UCL] Brunelle, F Robert, J J Nihoul-Fékété, C Saudubray, J M Junien, C. (2001) The American journal of pathology — Vol. 158, no. 6, p. 2177-84 (2001)
    • Journal article
    Loss of imprinted genes and paternal SUR1 mutations lead to focal form of congenital hyperinsulinism.
    Fournet, J C Mayaud, C de Lonlay, P Verkarre, V Rahier, Jacques[UCL] Brunelle, F Robert, J J Nihoul-Fékété, C Saudubray, J M Junien, C. (2000) Hormone research — Vol. 53 Suppl 1, p. 2-6 (2000)
    • Journal article
    The surgical management of congenital hyperinsulinemic hypoglycemia in infancy.
    Fékété, C Nihoul de Lonlay, P Jaubert, F Rahier, Jacques[UCL] Brunelle, F Saudubray, J M (2004) Journal of pediatric surgery — Vol. 39, no. 3, p. 267-9 (2004)
    • Journal article
    Pancreatic arterial calcium stimulation in the diagnosis and localisation of persistent hyperinsulinemic hypoglycaemia of infancy.
    Chigot, V De Lonlay, P Nassogne, Marie-Cécile[UCL] Laborde, K Delagne, V Fournet, J C Nihoul-Fékété, C Saudubray, J M Brunelle, F (2001) Pediatric radiology — Vol. 31, no.9, p. 650-655 (2001)
    • Journal article
    A broad spectrum of clinical presentations in congenital disorders of glycosylation I: a series of 26 cases.
    de Lonlay, P Seta, N Barrot, S Chabrol, B Drouin, V Gabriel, B M Journel, H Kretz, M Laurent, J Le Merrer, M Leroy, A Pedespan, D Sarda, P Villeneuve, N Schmitz, J Van Schaftingen, Emile[UCL] Matthijs, G Jaeken, J Korner, C Munnich, A Saudubray, J M Cormier-Daire, V (2001) Journal of Medical Genetics : an international peer-reviewed journal for health professionals and researchers in all areas of genetics — Vol. 38, no.1, p. 14-9 (2001)
    • Journal article
    Partial elective pancreatectomy is curative in focal form of permanent hyperinsulinemic hypoglycaemia in infancy: A report of 45 cases from 1983 to 2000.
    Crétolle, C[UCL] Fékété, C Nihoul Jan, D Nassogne, Marie-Cécile[UCL] Saudubray, J M Brunelle, F Rahier, Jacques[UCL] (2002) Journal of pediatric surgery — Vol. 37, no. 2, p. 155-8 (2002)
    • Journal article
    Hyperinsulinisme persistant du nouveau-né et du nourrisson: traitement chirurgical des lésions pancréatiques focales dans 60 cas.
    Crétolle, C de Lonlay, P Sauvat, F Brunelle, F Rahier, Jacques[UCL] Saudubray, J M Nihoul-Fékété, C (2005) Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie — Vol. 12, no. 3, p. 258-63 (2005)
    • Journal article
    Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia.
    Verkarre, V Fournet, J C de Lonlay, P Gross-Morand, M S Devillers, Martine[UCL] Rahier, Jacques[UCL] Brunelle, F Robert, J J Nihoul-Fékété, C Saudubray, J M Junien, C. (1998) The Journal of clinical investigation — Vol. 102, no. 7, p. 1286-91 (1998)
    • Journal article
    Mitochondrial respiratory chain defect: a new etiology for neonatal cholestasis and early liver insufficiency.
    Goncalves, I Hermans, Dominique[UCL] Chretien, D Rustin, P Munnich, A. Saudubray, J M Van Hoof, François[UCL] Reding, Raymond[UCL] de Ville de Goyet, J Otte, Jean-Bernard[UCL] (1995) Journal of hepatology — Vol. 23, no. 3, p. 290-4 (1995)
    • Journal article
    Pancreatic B-cell proliferation in persistent hyperinsulinemic hypoglycemia of infancy: an immunohistochemical study of 18 cases.
    Sempoux, Christine[UCL] Guiot, Yves[UCL] Dubois, D. Nollevaux, Marie-Cécile[UCL] Saudubray, J M Nihoul-Fekete, C Rahier, Jacques[UCL] (1998) Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc — Vol. 11, no. 5, p. 444-9 (1998)
    • Journal article
    Nésidioblastose et hyperinsulinisme néonatal persistant.
    Rahier, Jacques[UCL] Sempoux, Christine[UCL] Poggi, F Brunelle, F Saudubray, J M Fekete, C (1995) Journées annuelles de diabétologie de l'Hôtel-Dieu — , p. 73-82 (1995)
    • Journal article
    Neonatal hyperinsulinemic hypoglycemia: heterogeneity of the syndrome and keys for differential diagnosis.
    Sempoux, Christine[UCL] Guiot, Yves[UCL] Lefevre, A. Nihoul-Fékété, C Jaubert, F Saudubray, J M Rahier, Jacques[UCL] (1998) The Journal of clinical endocrinology and metabolism — Vol. 83, no. 5, p. 1455-61 (1998)
    • Journal article
    Partial or near-total pancreatectomy for persistent neonatal hyperinsulinaemic hypoglycaemia: the pathologist's role.
    Rahier, Jacques[UCL] Sempoux, Christine[UCL] Fournet, J C Poggi, F Brunelle, F Nihoul-Fekete, C Saudubray, J M Jaubert, F (1998) Histopathology — Vol. 32, no. 1, p. 15-9 (1998)
    • Journal article
    Liver transplantation in mitochondrial respiratory chain disorders.
    Sokal, Etienne[UCL] Sokol, R Cormier, V Lacaille, F McKiernan, P Van Spronsen, F J Bernard, O. Saudubray, J M (1999) European journal of pediatrics — Vol. 158 Suppl 2, p. S81-4 (1999)
    • Journal article
    Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasia.
    Fournet, J C Verkarre, V De Lonlay, P Rahier, Jacques[UCL] Brunelle, F Robert, J J Nihoul-Fékété, C Saudubray, J M Junien, C. (1998) Annales d'endocrinologie — Vol. 59, no. 6, p. 485-91 (1998)
    • Journal article
    Nesidioblastosis and persistent neonatal hyperinsulinism.
    Sempoux, Christine[UCL] Poggi, F Brunelle, F Saudubray, J M Fekete, C Rahier, Jacques[UCL] (1995) Diabète & métabolisme — Vol. 21, no. 6, p. 402-7 (1995)
    • Journal article
    Phosphomannose isomerase deficiency: a carbohydrate-deficient glycoprotein syndrome with hepatic-intestinal presentation.
    Jaeken, J Matthijs, G Saudubray, J M Dionisi-Vici, C Bertini, E de Lonlay, P Henri, H Carchon, H Schollen, E Van Schaftingen, Emile[UCL] (1998) American Journal of Human Genetics — Vol. 62, no.6, p. 1535-9 (1998)