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J-C Fournet

Showing results (41-50 of 48) with videos related to

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The Journal of Clinical Investigation|October 14, 1998
Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasiaV Verkarre, J C Fournet, P de Lonlay, 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.
The American Journal of Pathology|June 8, 2001
Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11J C Fournet, C Mayaud, P de Lonlay, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 14, 1999
[Persistent hyperinsulinemic hypoglycemia in the newborn and infants]P de Lonlay-Debeney, J C Fournet, D Martin, et al.
Archives of Pathology & Laboratory Medicine|October 28, 1997
Renal chromophobe cell carcinoma and oncocytoma. A comparative morphologic, histochemical, and immunohistochemical study of 124 casesB Cochand-Priollet, V Molinié, J Bougaran, et al.
The Journal of Clinical Investigation|August 15, 1997
Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomyP de Lonlay, J C Fournet, J Rahier, et al.
Journal of Medical Genetics|August 6, 2010
ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinismC Bellanné-Chantelot, C Saint-Martin, M-J Ribeiro, et al.
Journal of Medical Genetics|July 22, 2005
Congenital hyperinsulinism and mosaic abnormalities of the ploidyI Giurgea, D Sanlaville, J-C Fournet, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
The Journal of Clinical Investigation|October 14, 1998
Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasiaV Verkarre, J C Fournet, P de Lonlay, 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.
The American Journal of Pathology|June 8, 2001
Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11J C Fournet, C Mayaud, P de Lonlay, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 14, 1999
[Persistent hyperinsulinemic hypoglycemia in the newborn and infants]P de Lonlay-Debeney, J C Fournet, D Martin, et al.
Archives of Pathology & Laboratory Medicine|October 28, 1997
Renal chromophobe cell carcinoma and oncocytoma. A comparative morphologic, histochemical, and immunohistochemical study of 124 casesB Cochand-Priollet, V Molinié, J Bougaran, et al.
The Journal of Clinical Investigation|August 15, 1997
Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomyP de Lonlay, J C Fournet, J Rahier, et al.
Journal of Medical Genetics|August 6, 2010
ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinismC Bellanné-Chantelot, C Saint-Martin, M-J Ribeiro, et al.
Journal of Medical Genetics|July 22, 2005
Congenital hyperinsulinism and mosaic abnormalities of the ploidyI Giurgea, D Sanlaville, J-C Fournet, et al.
Pageof 5