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17篇 您的检索式:作者名="FOURNET JC"
    题名 作者 年代 出处 被引量
1Unbalanced ex- pression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosi- ty of a mutation in ABCC8 or KCNJll显示文摘Fournet JC Mayaud C de Lonlay P 2001Am J Pathol2001,158,6:1
2The genetics of neonatal hyperinsulinism显示文摘Fournet JC Junien C 2003HormRes2003,59,1:1
3Inflammatory pseudotumor of the liver: a rare benign tumor mimicking a malignancy显示文摘Lacaille F Fournet JC Sayegh N 1999Liver Transpl Surg1999,5,1:1
4Genetics of congential hyperinsulinism显示文摘FOURNET JC JUNIEN C 2004Endor Pathol2004,15,3:1
5Unbalanced expression of 11 p15 im- printed genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJll 显示文摘Fournet JC Mayaud C de LP 2001Am J Pathol2001,158,6:1
6Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism:association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11显示文摘Fournet JC Mayaud C de Lonlay P 0,,:1
7Iteterogeneity of persistent hyperinsulinaemic hypaglycaemia, a series of 175 cases 显示文摘de Lonlay P Fournet JC Touati G 2002Eur J Pediatr2002,161,1:1
8The genetics of neonatal hyperinsulinism 显示文摘Fournet JC Junien C 2003Horm Res2003,59,1:1
9Centrilobular necrosis in children after combined liver and small bowel transplantation显示文摘Lacaille F Canioni D Fournet JC 2002Transplantation2002,73,2:1
10Detection of molecular cytogenetic aberrations in Langerhans cell histiocytosis of bone 显示文摘Murakami I Gogusev J Fournet JC et ol 2002Hum Pathol2002,33,5:1
11Eosinophilic esophagnitis in children:symptoms,histology and pH probe results显示文摘Sant'Anna AM Rolland S Fournet JC 2004J Pediatr Gastroenterol Nutr2004,39,4:1
12Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: Association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ1 l显示文摘Fournet JC Mayaud C de Lonlay P 2001Am J Pathol2001,158,6:1
13Congenital hyper- insulinism and mosaic abnormalities of the ploidy 显示文摘Giurgea I Sanlaville D Fournet JC 2006J Med Genet2006,43,3:1
14Clinical aspects and course of neonatal hyperinsulinism显示文摘de Lonlay-Debeney P Poggi-Travert F Fournet JC 1999N Engl J Med1999,340,15:1
15Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinemia in focal adenomatous hyperplasia显示文摘Verkarre V Fournet JC de Lonlay P 1998J Clin Invest1998,102,7:1
16Value of open lung biopsy in immunocompromised children显示文摘 Morais L Fournet JC 2000J Pediatr2000,137,2:1
17Detection of mo- lecular cytogenetie aberrations in Langerhans cell histioeytosis of bone显示文摘Murakami I Gogusev J Fournet JC 2002HumPathol2002,33,5:1
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