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11篇 您的检索式:作者名="Caputo R."
    题名 作者 年代 出处 被引量
1Nuclear DNA contents, rDNAs, and karyotype evolution in subgenus Vicia : III. The heterogeneous section Hypechusa显示文摘P. Caputo M. Frediani G. Venora C. Ravalli M. Ambrosio R. Cremonini 2006Protoplasma2006,,4:1
2Numerical–experimental investigation on post-buckled stiffened composite panels显示文摘F. Caputo R. Esposito P. Perugini D. Santoro 2002Composite Structures2002,,3:1
3Nuclear DNA contents, rDNAs, and karyotype evolution in Vicia subgenus Vicia : II. Section Peregrinae显示文摘M. Frediani P. Caputo G. Venora C. Ravalli M. Ambrosio R. Cremonini 2005Protoplasma2005,,3:1
4A measurement of the ratio of the nucleon structure function in copper and deuterium显示文摘J. Ashman B. Badelek G. Baum J. Beaufays C. P. Bee C. Benchouk I. G. Bird S. C. Brown M. C. Caputo H. W. K. Cheung J. S. Chima J. Ciborowski R. Clifft G. Coignet F. Combley G. Court G. d’Agostini J. Drees M. Düren N. Dyce A. W. Edwards M. Edwards T. Ernst 1993Zeitschrift für Physik C Particles and Fields1993,,2:1
5Karyological and molecular characterisation of subgenus Vicia (Fabaceae)显示文摘P. Caputo M. Frediani M. T. Gelati G. Venora R. Cremonini M. Ruffini Castiglione 2013Plant Biosystems - An International Journal Dealing with all Aspects of Plant Biology2013,,4:1
6Cytological and molecular characterization of Vicia barbazitae Ten. & Guss.显示文摘M. Ruffini Castiglione M. Frediani M. Gelati G. Venora L. Giorgetti P. Caputo R. Cremonini 2012Protoplasma2012,,3:1
7成人与儿童Wells综合征:19例病例报道显示文摘Background: Wells syndrome, an uncommon inflammatory dermatosis, is characterized by protean cutaneous manifestations, suggestive but not specific histopathologic findings, and usually a recurrent course. Because of its original description as a distinct entity, it has come to be regarded as an abnormal eosinophilic response to a number of causative agents. Observations: The medical records of 19 patients (12 adults and 7 children) with Wells syndrome referred to the Institute of Dermatological Sciences from 1990 to 2005 were evaluated for the type and prevalence of skin lesions, clinical course and response to treatment, and possibly associated systemic symptoms, as well as histologic, laboratory, and immunofluorescence findings. The classic plaque-type variant proved to be the most common presentation in children but not in adults, who more frequently had the annular granuloma-like variant. Unilesional forms were found to occur more frequently in children. The course was recurrent, although slowly progressing, with amean duration of disease of 5 years for adults and 3 years for children. Conclusions: We emphasize the concept that the diagnosis of Wells syndrome is a clinicopathologic diagnosis. Although it should be classified within a spectrum that includes multisystem eosinophilic disorders, such as Churg-Strauss and hypereosinophilic syndromes, Wells syndrome, which has 7 variants, is a distinct cutaneous disease lacking systemic involvement.Caputo R. Marzano A.V. Vezzoli P Lunardon L. 潘敏 2006世界核心医学期刊文摘(皮肤病学分册)2006,,12:0
8兄妹共患网状红斑黏蛋白病Caputo R. Marzano A.V. Tourlaki A. Marchini M. 张路坤 2006世界核心医学期刊文摘(皮肤病学分册)2006,0,10:0
9他扎罗汀短期外用治疗寻常型银屑病显示文摘Background: We present the results of a multicentre, not controlled, clinical study on the tolerability and efficacy of tazarotene gel, used as short contact therapy (SCT), in psoriasis vulgaris. Objective: To evaluate whether irritant contact dermatitis caused by tazarotene was less frequent and/or less severe with SCT than with traditional therapy, and whether SCT with tazarotene was as effective as traditional therapy. Methods: Forty-three patients with plaque psoriasis were treated by SCT with 0.1% tazarotene gel (once daily application for 20 min, followed by washing with water). Treatment duration was 45 days. Results: Irritant contact dermatitis caused by tazarotene used as SCT was much less frequent and severe than traditional treatment with the same drug. SCT with tazarotene was effective in the treatment of plaque psoriasis. Conclusion: Tazarotene, used as SCT, was better tolerated than the same drug used as traditional treatment. Furthermore, SCT appeared to be as effective as traditional therapy with the same drug.Veraldi S. Caputo R. Pacifico A. 李晓莉 2006世界核心医学期刊文摘(皮肤病学分册)2006,0,5:0
10多发性骨髓瘤合并慢性苔藓样角化病和发疹性角化性棘皮瘤样皮损1例Marzano A.V. Bellinvia M. Caputo R. Alessi E. 李晓莉 冯义国 2005世界核心医学期刊文摘(皮肤病学分册)2005,0,7:0
11青少年阴囊坏疽性血管炎:坏疽性脓皮病的一种变异型?Caputo R. Marzano A.V. Di Benedetto A. 董平 2006世界核心医学期刊文摘(皮肤病学分册)2006,0,11:0
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