维普期刊资源整合服务平台（V6.5）

43篇 您的检索式：作者名="Lonlay P"

选中清除导出查看参考文献查看引证文献引用追踪共3页首页上一页第1页下一页末页 /3 跳转

	题名	作者	年代	出处	被引量
1	Unbalanced 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	2001	Am J Pathol2001，158，6：	1
2	Clinical approach to inherited metabolic disorders in neonates:an overview显示文摘	Saudubray JM Nassogne MC de Lonlay P	2002	Semin Neonatol2002，7，1：	1
3	Clinical ap- proach to inherited metabolic disorders in neonates:an overview 显示文摘	Saudubray JM Nassogne MC de Lonlay P Touati G	2002	Samin Neonatol2002，7，1：	1
4	Hyperinsulinaemic hy- poglycaemia: biochemical basis and the importance of maintaining nor- moglycaemia during management 显示文摘	Hussain K Blankenstein O De Lonlay P	2007	Arch Dis Child2007，92，7：	1
5	Clinical approach to inherited metabolic disorders in neonates: an overview 显示文摘	Saudubray JM Nassogne MC de Lonlay P Touati G	2002	Semin Neonatal2002，7，1：	1
6	KATP channel muta- tions in congenital hyperinsulinism 显示文摘	Saint - Martin C Arnoux JB de Lonlay P	2011	Semin Pediatr Surg2011，20，1：	1
7	Clinical approach to inherited metabolic disorders in neonates: an overview 显示文摘	Saudubray JM Nassogne MC Lonlay P	2002	Semin Neonatol2002，7，1：	1
8	Paternal mutation of the sulfonylurea receptor(SUR1)gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia显示文摘	Verkarre V Foumet JC de Lonlay P		0，，：	1
9	Recognition and management of fatty acid oxidation defects:a series of 107 patients显示文摘	Saudubray JM Martin D de Lonlay P	1999	J Inherit Metab Dis1999，22，：	1
10	Clinical approach to inherited metabolic disorders in neonates an overview显示文摘	Saudubray J M Nassognc M C de Lonlay P	2002	Semin Neonatol2002，7，1：	1
11	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显示文摘	Fournet JC Mayaud C de Lonlay P		0，，：	1
12	Congenilal hyperinsulinism 显示文摘	Arnoux JB de Lonlay P Ribeiro MJ	2010	Early Human Development2010，86，5：	1
13	Iteterogeneity of persistent hyperinsulinaemic hypaglycaemia, a series of 175 cases 显示文摘	de Lonlay P Fournet JC Touati G	2002	Eur J Pediatr2002，161，1：	1
14	Congenital hyperinsulinism: pancreatic fluoro-L- dihydroxyphenylalanine (DOPA) positron emission tomography and immunohistochcmistry study of DOPA decarboxylase and insulin secretion 显示文摘	De Lonlay P Simon-Carre A Ribeiro MJ	2006	J Clin Endocrinol Metab2006，91，3：	1
15	Congenital hyperinsulinism显示文摘	Arnoux JB De Lonlay P Ribeiro MJ	2010	Early Hum Dev2010，86，5：	1
16	Topography of brain dam- age in metabolic hypoglyeaemia is determined by age at which hypogly- caemia occurred显示文摘	Gataullina S De Lonlay P Dellatolas G	2013	Dev Med Child Neuml2013，55，2：	1
17	Hyperinsulinaemic hypoglycaemia: biochemical basis and the importance of maintaining normoglycaemia during management 显示文摘	Hussain K Blankensteln O De Lonlay P	2007	Arch Dis Child2007，92，2：	1
18	KATP channel mutations in congenital hyperinsulinism显示文摘	Saint-Martin C Arnoux JB de Lonlay P		0，，：	1
19	Cerebral white matter disease in children may be caused by mitochondrial respiratory chain defi- ciency显示文摘	de Lonlay Debeney P von Kleist Retzow J C Hertz-Pan- nier L	2000	J Pediatr2000，136，2：	1
20	Unbalanced 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	2001	Am J Pathol2001，158，6：	1

返回顶部每页显示：

共3页首页上一页第1页下一页末页 /3 跳转

互联网出版许可证新出网证(渝)字10号全国400电话 - 免长途话费

用户提示