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E. Cinotti B. Labeille S. Debarbieux C. Carrera F. Lacarrubba A.M. Witkowski E. Moscarella E. Arzberger H. Kittler P. Bahadoran S. Gonzalez P. Guitera M. Agozzino F. Farnetani R. Hofmann‐Wellenhof M. Ardigò P. Rubegni L. Tognetti J. Łudzik I. Zalaudek G. Argenziano C. Longo S. Ribero J. Malvehy G. Pellacani F. Cambazard J.L. Perrot 《Journal of the European Academy of Dermatology and Venereology》2018,32(8):1284-1291
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E. Cinotti J.L. Perrot B. Labeille F. Cambazard 《Journal of the European Academy of Dermatology and Venereology》2016,30(5):754-763
Reflectance confocal microscopy (RCM) is a high‐resolution emerging imaging technique that allows non‐invasive diagnosis of several cutaneous disorders. A systematic review of the literature on the use of RCM for the study of infections and infestations has been performed to evaluate the current use of this technique and its possible future applications in this field. RCM is particularly suitable for the identification of Sarcoptes scabies, Demodex folliculorum, Ixodes, Dermatophytes and Candida species in the clinical practice and for the follow‐up after treatment. The cytopathic effect of herpes simplex virus, varicella zoster virus and molluscipoxvirus is also detectable by this imaging technique even in a pre‐vesicular stage. In addition, thanks to its non‐invasiveness, RCM allows pathophysiological studies. 相似文献
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Mucosal melanoma: clinical,histological and c‐kit gene mutational profile of 86 French cases 下载免费PDF全文
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A. Messori M. Morfini M. Blomback S. Cinotti G. Longo K. Schimpf K. Schumacher A. Novakova-Banet U. Delvos H. Kjellman 《Thrombosis research》1992,65(6):699-708
We assessed the pharmacokinetic characteristics of a new high-purity pasteurized FVIII concentrate in comparison with an intermediate purity pasteurized concentrate, produced by the same manufacturer. The study was designed as a cross-over single-dose pharmacokinetic investigation in 8 non-bleeding patients with severe hemophilia A. All patients were given 25 IU/kg of each of the two concentrates, with an interval of at least one week between the two administrations. Decay curves were assessed by collecting 10 serial blood samples over 36 hours following the end of infusion. The concentration of Factor VIII in blood samples was determined in triplicate in three different laboratories using each of the following assay methods: a one-stage clotting assay, a two-stage clotting assay, and a two-stage chromogenic-peptide substrate assay. All pharmacokinetic parameters were calculated by model-independent methods. The two products were found to differ significantly both in the clearance, which was on average 13.8% lower for Haemate P, and in the in-vivo recovery, which was 11.7% lower for Factor VIII:C P on the average. In comparison with previous pharmacokinetic data obtained from other heated Factor VIII concentrates, the clearance of Haemate P was found to be significantly slower, while the half-life of both products was longer. No differences were observed in the Vd-area. These findings indicate that the purification procedures to which both products are subjected do not increase the in-vivo rate of plasma disappearance of Factor VIII. 相似文献