维普中文期刊产品整合服务
25篇 您的检索式:作者名="Lesca G"
    题名 作者 年代 出处 被引量
1The adult form of Niemann-Pick disease type C显示文摘Sévin M Lesca G Baumann N 2007Brain2007,130,1:1
2GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction显示文摘Lesca G Rudolf G Bruneau N 2013Nat Genet2013,45,9:1
3Molecular screening of ALKI/ACVRL1 and ENG gene in Hereditary hemorrhagic telangiectasia in France显示文摘LESCA G PLAUCH H COULET F 2004Hum Mutat2004,23,:1
4Molecular screening of ALK1/ACVRL1and ENG genes in hereditary hemorrhagic telangiectasia in France显示文摘LESCA G PLAUCHU H COULET F 2004Hum Mutat2004,23,:1
5GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction显示文摘Lesca G Rudolf G Bruneau N 2013Nature Genetics2013,45,:1
6Genotype-pheno- type correlations in hereditary hemorrhagic telangiectasia: da- ta from the French-Italian HHT network 显示文摘Lesca G Olivieri C Burnichon N 2007Genet Med2007,9,1:1
7The adult form of Niemann-Pick disease type C 显示文摘Sevin M Lesca G Baumann N 2007Brain2007,130,:1
8Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types:genomic dissection makes the link with autism显示文摘Lesca G Rudolf G Labalme A 0,,09:1
9Molecular screening of ALK1/ACVRL1 and ENG genes in hereditary hemorrhagic telangiectasia in France显示文摘Lesca G Plauchu H Coulet F 0,,04:1
10Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types: genomic dissection makes the link with autism显示文摘Lesca G Rudolf G Labalme A 2012Epilepsia2012,53,:1
11Pulmonary vascular manifestations of hereditary hemorrhagic telangiectasia ( rendu-osler disease) 显示文摘Cottin V Dupuis-Girod S Lesca G el al 2007Respiration2007,74,4:1
12Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types:genomic dissection makes the ]ink with autlsm显示文摘Lesca G Rudolf G Labalme A 2012Epilepsia2012,53,9:1
13ANRIL Expression Is Associated With Atherosclerosis Risk at Chromosome 9p21显示文摘Lesca M. Holdt Frank Beutner Markus Scholz Stephan Gielen Gábor G?bel Hendrik Bergert Gerhard Schuler Joachim Thiery Daniel Teupser 2010Arteriosclerosis Thrombosis and Vascular Biology2010,,3:1
14Pulmonary vascular manifestations of hereditary hemorrhagic telangiectasia (rendu-osier disease) 显示文摘Cottin V Dupuis Girod S Lesca G 2007Respiration2007,74,4:1
15Symptomatic carriers of dystrophinopathy with chromosome X inactivation bias显示文摘Lesca G Demarquay G Llense S 2003Rev Neurol (Paris)2003,159,89:1
16Selective pelvic arterial em-bolization in the management of obstetric hemorrhage显示文摘Vegas G Lescas T Munoz M 2006Eur JObstet Gynecol Repord Biol2006,127,1:1
17Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types:genomic dissection makes the link with autism显示文摘Lesca G Rudolf G Labalme A 0,,9:1
18Pulmonary vascular manifestations of hereditary hemorrhagic telangiectasia (renduosler disease)显示文摘Cottin V Dupuis-Girod S Lesca G 0,,:1
19Long-term Follow-up in 12 Children with Pulmonary Arteriovenous Malformations:Confirmation of Hereditary Hemorrhagic Telangiectasia in All Cases显示文摘Curie A Lesca G Cottin V 2007J Pediatr2007,151,3:1
20Pulmonary vascular mani- festations of hereditary hemorrhagic telangiectasia (Rendu-Osler disease) 显示文摘Cottin V Dupuis-Girod S Lesca G 2007Respiration2007,74,4:1
返回顶部 每页显示:
共2页 首页 上一页 第1页 下一页 末页 /2 跳转

网站首页 | 关于我们 | 联系我们 | 产品服务 | 客服中心 | 广告服务 | 版权声明 | 网站联盟 | 友情链接 | 售卡网点

版权所有© 渝B2-20050021-1 渝公网安备 50019002500403号 违法和不良信息举报中心

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