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28篇 您的检索式:作者名="GRAMLICH I"
    题名 作者 年代 出处 被引量
1Quantification of mRNA degradation as possible indicator of post- mortem interval-a pilot study显示文摘Bauer M Gramlich I Polzin S 2003Leg Med(Tokyo)2003,5,4:1
2Quantification of mRNA degradation as possible indicator of postmortem interval--a pilot study显示文摘BAUER M GRAMLICH I POLZIN S 2003Leg Med (Tokyo)2003,5,4:1
3Quantification of mRNA degradation as possible indicator of postmortem interval a pilot study 显示文摘Bauer M Gramlich I Polzin S 2003Leg Med2003,5,4:1
4Quantification of mRNA degradation as possible indicator of postmortem interval-a pilot study显示文摘Bauer M Gramlich I Polzin S 2003Leg Med2003,5,4:1
5Novel, Highly Nonlinear Optical Molecular Crystals Based on Multidonor-Substituted 4-Nitrophenylhydrazones显示文摘Liakatas I Wong M S Gramlich V 1998Adv Mater1998,10,:1
6Quantification of mRNA degradation as possible indicator of postmortem interval-a pilot study显示文摘Bauer M Gramlich I Polzin S 2003Leg Med(Tokyo)2003,5,4:1
7Quantification of mRNA degradation as possible indicator of postmortem intervala pilot study显示文摘Bauer M Gramlich I Polzin S 0,,05:1
8Novel, High Nonlinear Optical Molecular Crystals Based on MultidonorSubstituted 4-Nitrophenylhydrazones显示文摘 Wong M S Gramlich V 1998Advanced Materials1998,10,:1
9Quantification of mRNA degradation as possible indicator of postmortem interval - a pilot study 显示文摘Bauer M Gramlich I Polzin S 2003Leg Med (Tokyo)2003,5,4:1
10Quantification of mRNA degradation as possible indicator of postmortem interval--a pilot study显示文摘Bauer M Gramlich I Polzin S 2003Legal Med (Tokyo)2003,5,4:1
11Quantification of mRNA degradation as possible indicator of postmortem interval-a pilot study 显示文摘Bauer M Gramlich I Polzin S 2003Leg Med2003,5,4:1
12Quantification of mRNA degradation as possible indicator of postmortem intervala pilot study显示文摘Bauer M Gramlich I Polzin S 0,,05:1
13A treatment algorithm for neuropathic pain显示文摘Namaka M Gramlich CR Ruhlen D Melanson M Sutton I Major J 0,,:1
14Improved canine model for laryngotracheal stenosis显示文摘Eliashar R Elisehar I Gramlich T 2000Otolaryngol Head Neck Surg2000,122,1:1
15Quantification of mRNA degradation as possible indicator of postmortem interval-a pilot study显示文摘Bauer M Gramlich I Polzin S 2003Leg Med(Tokyo)2003,5,4:1
16Quantification of mRNA degradation as possible indicator of postmortem interval a pilot study 显示文摘Bauer M Gramlich I Polzin S 2003Leg Med2003,5,4:1
17Quantification of mRNA degradation as possible indicator of postmortem interval - a pilot study显示文摘Bauer M Gramlich I Silke Patzelt D 2003Leg Med2003,5,4:1
18Use of parenteral nutrition in patients with advanced cancer显示文摘Soo I Gramlich L 2008Appl Physiol Nutr Metab2008,33,1:1
19Improved canine model for laryngotracheal stenosis显示文摘Eliashar R Eliachar I Gramlich T 2000Otolaryngol Head Neck Surg2000,122,:1
20Crohn's disease genotypes of patients in remission vs relapses after infliximab discontinuation显示文摘AIM:To investigate genetic differences between Crohn's disease(CD) patients with a sustained remission vs relapsers after discontinuing infliximab while in corticosteroid-free remission.METHODS:Forty-eight CD patients received infliximab and were in full corticosteroid-free clinical remission but then discontinued infliximab for reasons other than a loss of response,were identified by review of an electronic database and charts.Infliximab-associated remission was defined as corticosteroid-free plus normalization of clinical disease activity [CD activity index(CDAI) < 150] during follow-up visits based on physician global assessments.A CD relapse(loss of infliximab-induced remission) was clinically defined as a physician visit for symptoms of disease activity(CDAI > 220) and a therapeutic intervention with CD medication(s),or a hospitalization with complications related to active CD.Genetic analyses were performed on samples from 14 patients(n = 6 who had a sustained long term remission after stopping infliximab,n = 8 who rapidly relapsed after stopping infliximab).Nucleotide-binding oligomerization domain 2(NOD2)/caspase activation recruitment domain 15(CARD15) polymorphisms(R702W,G908R and L1007fs) and the inflammatory bowel disease 5(IBD5) polymorphisms(IGR2060a1 and IGR3081a1) were analyzed in each group.RESULTS:Five single nucleotide polymorphisms of IBD5 and NOD2/CARD15 genes were successfully analyzed for all 14 subjects.There was no significant increase in frequency of the NOD2/CARD15 polymorphisms(R702W,G908R and L1007fs) and the IBD5 polymorphisms(IGR2060a1 and IGR3081a1) in either group of patients;those whose disease relapsed rapidly or those who remained in sustained long term remission following the discontinuation of infliximab.Nearly a third of patients in full clinical remission who stopped infliximab for reasons other than loss of response remained in sustained clinical remission,while two-thirds relapsed rapidly.There was a marked difference in the duration of clinical remission following discontinuance of infliximab between the two groups.The patients who lost remission did so after 1.0 years ± 0.6 years,while those still in remission were at the time of this study,8.1 years ± 2.6 years post-discontinuation of infliximab,P < 0.001.The 8 patients who had lost remission after discontinuing infliximab had a mean number of 5 infusions(range 3-7),with a mean treatment time of 7.2 mo(range 1.5 mo-15 mo).The mean duration of time from the last infusion of infliximab to the time of loss of remission was 382 d(range 20 d-701 d).The 6 patients who remained in remission after discontinuing infliximab had a mean number of 6 infusions(range 3-12),with a mean treatment duration of 12 mo(range 3.6 mo-32 mo)(P = 0.45 relative to those who lost remission).CONCLUSION:There are no IBD5 or NOD2/CARD15 mutations that predict which patients might have sustained remission and which will relapse rapidly after stopping infliximab.Cathy Lu Alistair Waugh Robert J Bailey Raeleen Cherry Levinus A Dieleman Leah Gramlich Kata Matic Mario Millan Karen I Kroeker Daniel Sadowski Christopher W Teshima Dennis Todoruk Clarence Wong Karen Wong Richard N Fedorak 2012World Journal of Gastroenterology2012,18,36:1
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