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1.
Didier Mathieu Alain Rahmouni Norbert Vasile Nedal Jazaerli Christophe Duvoux Jeanne Tran Van Nhieu Elie Serge Zafrani 《Journal of magnetic resonance imaging : JMRI》1994,4(3):506-508
This case report illustrates atypical magnetic resonance (MR) imaging findings in a liver hemangioma mimicking a malignant lesion—lower signal intensity than cerebrospinal fluid on T2-weighted spin-echo images and lack of early enhancement on dynamic contrast material—enhanced gradient-echo images. Pathologic analysis demonstrated nearly total replacement of the vascular cavities by dense fibrous tissue. In this rare, sclerosed form, this lesion could not be defined as a hemangioma with MR imaging. 相似文献
2.
Plasmid-mediated beta-lactamase (TEM-7) involved in resistance to ceftazidime and aztreonam 总被引:23,自引:0,他引:23
L Gutmann M D Kitzis D Billot-Klein F Goldstein G Tran Van Nhieu T Lu J Carlet E Collatz R Williamson 《Reviews of infectious diseases》1988,10(4):860-866
TEM-7, a novel TEM-type beta-lactamase (pI 5.41) encoded on a plasmid of approximately 85 kilobases, was found in a clinical isolate of Citrobacter freundii. Strains containing this enzyme exhibited decreased susceptibility to ceftazidime (64-fold) and aztreonam (16-fold) but not to other third-generation cephalosporins. Addition of a beta-lactamase inhibitor--clavulanic acid, sulbactam, or YTR 830--restored normal susceptibility to associated compounds such as ampicillin, piperacillin, ceftazidime, and aztreonam. DNA-DNA hybridization of an intragenic probe of TEM-1 occurred with a 19-kilobase EcoRI fragment of the plasmid encoding TEM-7. A TEM-2 derivative, TEM-201, with characteristics similar to those of TEM-7 was selected spontaneously in the presence of ceftazidime in vitro. 相似文献
3.
Antifibrogenic role of the cannabinoid receptor CB2 in the liver 总被引:10,自引:0,他引:10
Julien B Grenard P Teixeira-Clerc F Van Nhieu JT Li L Karsak M Zimmer A Mallat A Lotersztajn S 《Gastroenterology》2005,128(3):742-755
4.
Golli M; Van Nhieu JT; Mathieu D; Zafrani ES; Cherqui D; Dhumeaux D; Vasile N; Rahmouni A 《Radiology》1994,190(3):741
5.
Transfer of amikacin resistance by closely related plasmids in members of the family Enterobacteriaceae isolated in Chile. 总被引:2,自引:5,他引:2 下载免费PDF全文
G T Van Nhieu F W Goldstein M E Pinto J F Acar E Collatz 《Antimicrobial agents and chemotherapy》1986,29(5):833-837
During a 9-month period when amikacin was the sole aminoglycoside used clinically in a hospital in Santiago, Chile, resistance to amikacin and other antibiotics was encountered in 42 strains of the family Enterobacteriaceae, including Escherichia coli, Klebsiella pneumoniae, Citrobacter freundii, Enterobacter cloacae, Serratia marcescens, and Serratia liquefaciens. Amikacin resistance was transferable by conjugation and carried by IncM plasmids ranging in size from ca. 48.4 to 58.1 kilobase pairs. The plasmids had ca. 70 to 80% of their structure in common, as judged after digestion with restriction endonucleases. The resistance was mediated by a 6' aminoglycoside acetyltransferase. We conclude that selective pressure has favored the dissemination of a wide-host-range amikacin resistance plasmid and its derivatives. 相似文献
6.
7.
Association of CYP1B1 germ line mutations with hepatocyte nuclear factor 1alpha-mutated hepatocellular adenoma 总被引:3,自引:0,他引:3
Jeannot E Poussin K Chiche L Bacq Y Sturm N Scoazec JY Buffet C Van Nhieu JT Bellanné-Chantelot C de Toma C Laurent-Puig P Bioulac-Sage P Zucman-Rossi J 《Cancer research》2007,67(6):2611-2616
Biallelic somatic mutations of TCF1 coding for hepatocyte nuclear factor 1alpha (HNF1alpha) are found in 50% of the hepatocellular adenoma (HCA) cases usually associated with oral contraception. In rare cases, HNF1alpha germ line mutations could also predispose to familial adenomatosis. In order to identify new genetic factors predisposing to HNF1alpha-mutated HCA, we searched for mutations in genes involved in the metabolism of estrogen. For 10 genes (CYP1A1, CYP1A2, CYP3A4, CYP3A5, COMT, UGT2B7, NQO1, GSTM1, GSTP1, and GSTT1), we did not find mutations nor differences in the allele distribution among 32 women presenting HNF1alpha-mutated adenomas compared with 58 controls. In contrast, we identified a CYP1B1 germ line heterozygous mutation in 4 of 32 women presenting HNF1alpha-mutated adenomas compared with none in 58 controls. We confirmed these results with the identification of four additional CYP1B1 mutations in a second series of 26 cases. No mutations were found in the control group, which was extended to 98 individuals, and only a known rare genetic variant was observed in two controls (P = 0.0003). We did an ethoxyresorufin O-deethylase assay to evaluate the functional consequence of the CYP1B1 mutations. We found reduced enzymatic activity in each CYP1B1 variant. In addition, an E229K CYP1B1 mutation was found in a woman with a germ line HNF1alpha mutation in a familial adenomatosis context. In this large family, all three patients with adenomatosis bore both HNF1 and CYP1B1 germ line mutations. In conclusion, our data suggested that CYP1B1 germ line-inactivating mutations might increase the incidence of HCA in women with HNF1alpha mutations. 相似文献
8.
Activated protein C resistance acquired through liver transplantation and associated with recurrent venous thrombosis 总被引:15,自引:0,他引:15
Leroy-Matheron C Duvoux C Van Nhieu JT Leroy K Cherqui D Gouault-Heilmann M 《Journal of hepatology》2003,38(6):866-869
We report a new case of recurrent, extra-hepatic, deep vein thrombosis occurring after orthotopic liver transplantation for hepatocellular carcinoma complicating 'mixed' alcoholic and post-hepatitic C cirrhosis. Coagulation tests showed activated protein C resistance. The patient's genomic DNA was negative for the factor V Leiden mutation. Analysis of the grafted liver DNA showed that the donor was a heterozygous carrier of the factor V Leiden mutation and that the recipient's activated protein C resistance was acquired through the transplantation.Screening of candidate liver donors for a prothrombotic tendency is controversial. However, this case suggests that patients who develop venous thrombosis after liver transplantation should be screened for thrombophilic abnormalities, bearing in mind that genetic abnormalities which do not affect clotting test results, such as the G20210A mutation in the factor II gene, can only be diagnosed by testing the donor or graft. 相似文献
9.
This paper discusses the problems of visualizing new contact lens designs. We have developed computer-aided design (CAD) software that greatly improves lens visualization: this is illustrated for a spherical hydrophilic lens. Designers have the options of displaying magnified cross-sections of any part of the lens, making detailed measurements of these cross-sections, and displaying colour-coded three-dimensional views of the lens surfaces. Future developments are discussed. 相似文献
10.