维普中文期刊产品整合服务
9篇 您的检索式:作者名="Marc SE"
    题名 作者 年代 出处 被引量
1Effects of sleep deprivation and sleep fragmentation on upper airway collapsibility in normal subjects 显示文摘Se'rie's F Roy N Marc I 1994Am J Respir Crit Care Med1994,150,:1
2Activity of Pemetrexed (ALIMTA?, Multitargeted Antifolate, LY231514) in Metastatic Breast Cancer Patients Previously Treated with an Anthracycline and a Taxane: An Interim Analysis显示文摘Marc Spielmann Miguel Martin Mo?se Namer Andreas duBois Clemens Unger David J. Dodwell 2001Clinical Breast Cancer2001,,1:1
3Decompressive craniectomy for severe traumatic brain injury: Evaluation of the effects at one year*显示文摘Jacques Albanèse Marc Leone Jean-Roch Alliez Jean-Marc Kaya Fran?ois Antonini Bernard Alliez Claude Martin 2003Critical Care Medicine2003,,10:1
4Elevated levels of plasma creactive protein are associated with decreased graft survival in cardiac transplant recipients显示文摘Marc SE Hong JC Mark KW 2000Circulation2000,102,17:1
5Decompressive craniectomy for severe traumatic brain injury: Evaluation of the effects at one year*显示文摘Jacques Albanèse Marc Leone Jean-Roch Alliez Jean-Marc Kaya Fran?ois Antonini Bernard Alliez Claude Martin 2003Critical Care Medicine2003,,10:1
6Elevated levels of plasma C-reactive protein are associated with decreased graft survival in cardiac transplant recipients显示文摘Marc SE Hong JC Mark KW 2000Circulation2000,102,17:1
7Theoretical and experimental study of differential group de- lay and polarization dependent loss of Bragg gratings written in bireffingent fiber 显示文摘Se bastien Bette Christophe Caucheteur Marc Wuilpart 2007Opt Commun2007,269,:1
8Allogeneic stem cell transplantation-A curative treatment for paroxysmal nocturnal hemoglobinuria with PIGT mutation:A case report显示文摘BACKGROUND Patients with paroxysmal nocturnal hemoglobinuria(PNH)have a clonal population of blood cells deficient in glycosylphosphatidylinositol-anchored(GPIanchored)proteins,most of the time resulting from a mutation in the X-linked gene PIGA.We report a patient with PNH resulting from a rare biallelic PIGT mutation on chromosome 20.CASE SUMMARY A 47-year-old man was referred to our hospital for febrile pancytopenia.The patient reported a history of recurrent urticaria and arthralgia and he presented during 3 mo recurrent acute dermo-hypodermitis and aseptic meningitidis.Based on clinical cases published with PIGT-PNH,with clinically typical PNH and autoinflammatory symptoms,we treated our patients with repeated infusions of eculizumab to decrease autoinflammatory symptoms and then we performed an allogeneic stem cell transplantation(allo-SCT)with a mismatched unrelated donor.Our patient experienced no acute Graft vs Host disease(GvHD)and a moderate chronic GvHD and is now considered cured at 24 mo after allo-SCT.CONCLUSION This case report suggests that allo-SCT should be considered to cure PIGT-PNH patients.Laurence Schenone Anne-Béatrice Notarantonio Véronique Latger-Cannard Veronique Fremeaux-Bacchi Marcelo De Carvalho-Bittencourt Marie-Thérèse Rubio Marc Muller Maud D'Aveni 2022World Journal of Clinical Cases2022,10,17:0
9Genetic factors for differentiated thyroid cancer in French Polynesia:new candidate loci显示文摘Background:Populations of French Polynesia(FP),where France performed atmospheric tests between 1966 and 1974,experience a high incidence of differentiated thyroid cancer(DTC).However,up to now,no sufficiently large study of DTC genetic factors in this population has been performed to reach definitive conclusion.This research aimed to analyze the genetic factors of DTC risk among the native FP populations.Methods:We analyzed more than 300000 single nucleotide polymorphisms(SNPs)genotyped in 283 DTC cases and 418 matched controls born in FP,most being younger than 15 years old at the time of the first nuclear tests.We analyzed the genetic profile of our cohort to identify population subgroups.We then completed a genome-wide analysis study on the whole population.Results:We identified a specific genetic structure in the FP population reflecting admixture from Asian and European populations.We identified three regions associated with increased DTC risk at 6q24.3,10p12.2,and 17q21.32.The lead SNPs at these loci showed respective p-values of 1.66×10^(−7),2.39×10^(−7),and 7.19×10^(−7) and corresponding odds ratios of 2.02,1.89,and 2.37.Conclusion:Our study results suggest a role of the loci 6q24.3,10p12.2 and 17q21.32 in DTC risk.However,a whole genome sequencing approach would be better suited to characterize these factors than genotyping with microarray chip designed for the Caucasian population.Moreover,the functional impact of these three new loci needs to be further explored and validated.Monia Zidane Marc Haber Thérèse Truong Frédérique Rachédi Catherine Ory Sylvie Chevillard Hélène Blanché Robert Olaso Anne Boland Éric Conte Mojgan Karimi Yan Ren Constance Xhaard Vincent Souchard Jacques Gardon Marc Taquet André Bouville Jean-François Deleuze Vladimir Drozdovitch Florent de Vathaire Jean-Baptiste Cazier 2023Precision Clinical Medicine2023,6,2:0
返回顶部 每页显示:
共1页 首页 上一页 第1页 下一页 末页 /1 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