Hi, I'm using jabref to cite in libreoffice. I'm using numbers in the text to refer to the citations and need these numbers to be italicized.
Naively I thought that FormatCitations=true ItalicCitations=true in the style file would do the trick but It doesn't Also CitationCharacterFormat="Default Style" Doesn't seem to have any effect. I'm using Jabref 2.10 (2.9.2 had the same problem) on ubuntu linux 14.04 (13.10 was doing the same). My style file, a minimal bib file and the odt are attached. Thanks, Corentin -- ___________________ Corentin M. Barbu-Covantes (484) 843-1580 http://scholar.google.com/citations?hl=en&user=sxDMRdQAAAAJ "For what does it profit a man to gain the whole world, and forfeit his soul?" Mark 8:36
% This file was created with JabRef 2.10. % Encoding: ISO8859_1 @Article{Castro1976, Title = {Toxicity of methyl bromide and other gaseous insecticides to Triatoma infestans.}, Author = {Castro, J. A. and Zerba, E. N. and De Licastro, S. A. and Picollo, M. I. and Wood, E. J. and Ruveda, M. A. and De Moutier Aldao, E. M. and Libertella, R.}, Journal = {Acta Physiol Lat Am}, Year = {1976}, Number = {2}, Pages = {106--114}, Volume = {26}, Abstract = {Cuticular penetration of lipid soluble substances in Triatoma infestans is very poor (less than 1\% in 24 hr), while the respiratory route is particularly efficient (28\% in 5 min). Accordingly, several noxious gases killed the insect at short periods of time. CH3Br and SO2 were particularly effective and they also evidenced ovicide action. With the former compound this effect is also observed at low concentrations. The CH3Br hydrolysis products or its metabolites were not similarly effective, while other methylating agent, diazomethane, was very active. The irreversible binding of 14CH3Br to proteins and lipids of T. infestans, as well as the decrease in the sulfhydryl groups content of the proteins of the insect provoked by CH3Br suggest that this compound kills the insect because of its alkylating properties. The use of gaseous insecticides in the chemical control of T. infestans is discussed.}, Keywords = {Animals; Bromides, toxicity; Chagas Disease, prevention /&/ control; Insect Control; Insect Vectors; Respiration, drug effects; Skin Absorption; Sulfur Dioxide, toxicity; Triatoma; Triatominae}, Owner = {cbarbu}, Pmid = {829466}, Timestamp = {2009.02.17} } @Article{Litchfield1949, Title = {A simplified method of evaluating dose-effect experiments}, Author = {J. T. Litchfield and F. Wilcoxon}, Journal = {J Pharmacol Exp Ther}, Year = {1949}, Month = {Jun}, Number = {2}, Pages = {99--113}, Volume = {96}, Abstract = {The increased emphasis on quantitative biological studies in recent years has resulted in the widespread use of statistical methods for evaluating biological data. Much of this data is of the all-or-none type and, consequently, it is necessary to solve a dose-percent effect curve. By converting doses to logarithms and per cent effects to probits (1), logits (2), or angles (3), a straight line may be fitted by the method of weighted least squares. From the viewpoint of many biologists, such procedures are not pleasant to contemplate because the data must be converted to units which are meaningless to many and the calculations are difficult, tedious and often quite incomprehensible. It is not surprising therefore that there is widespread use of a variety of approximate methods for solving dose-per cent effect curves. It may be argued that such methods are undesirable because they do not make use of all of the information contained in the data, and are therefore inefficient in a statistical sense. On the other hand, the computations necessary in using efficient methods are often so time-consuming and laborious that the busy experimenter is deterred from using them, and thus loses the advantage of a statistical evaluation of his results. An examination of the various approximate methods, which have been proposed for the solution of dose-effect experiments of the all-or-none type, leads to the conclusion that none of them are entirely satisfactory in combining ease of computation with efficiency and accuracy. In order to appreciate this fact, it is helpful to list the essentials of a satisfactory approximate method for the solution of dose-effect experiments.}, File = {Litchfield1949.pdf:Litchfield1949.pdf:PDF}, Language = {eng}, Medline-pst = {ppublish}, Owner = {cbarbu}, Pmid = {18152921}, Timestamp = {2009.06.05} } @Article{Moncayo2003, Title = {Chagas Disease: Current Epidemiological Trends after the Interruption of Vectorial and Transfusional Transmission in the Southern Cone Countries}, Author = {Alvaro Moncayo}, Journal = {Mem Inst Oswaldo Cruz}, Year = {2003}, Number = {5}, Pages = {577-591}, Volume = {98}, Abstract = {Chagas disease, named after Carlos Chagas who first described it in 1909, exists only on the American Continent.It is caused by a parasite, Trypanosoma cruzi, transmitted to humans by blood-sucking triatomine bugs and by bloodtransfusion.Chagas disease has two successive phases, acute and chronic. The acute phase lasts 6 to 8 weeks. After severalyears of starting the chronic phase, 20% to 35% of the infected individuals, depending on the geographical areawill develop irreversible lesions of the autonomous nervous system in the heart, esophagus, colon and the peripheralnervous system. Data on the prevalence and distribution of Chagas disease improved in quality during the 1980s asa result of the demographically representative cross-sectional studies carried out in countries where accurateinformation was not available. A group of experts met in Bras\'ilia in 1979 and devised standard protocols to carryout countrywide prevalence studies on human T. cruzi infection and triatomine house infestation.Thanks to a coordinated multi-country program in the Southern Cone countries the transmission of Chagasdisease by vectors and by blood transfusion has been interrupted in Uruguay in1997, in Chile in 1999, and in 8 ofthe 12 endemic states of Brazil in 2000 and so the incidence of new infections by T. cruzi in the whole continent hasdecreased by 70%. Similar control multi-country initiatives have been launched in the Andean countries and inCentral America and rapid progress has been recorded to ensure the interruption of the transmission of Chagas disease by 2005 as requested by a Resolution of the World Health Assembly approved in 1998.The cost-benefit analysis of the investments of the vector control program in Brazil indicate that there aresavings of US$17 in medical care and disabilities for each dollar spent on prevention, showing that the program is a health investment with good return. Since the inception in 1979 of the Steering Committee on Chagas Disease of the Special Program for Research and Training in Tropical Diseases of the World Health Organization (TDR), the objective was set to promote and finance research aimed at the development of new methods and tools to control this disease.The well known research institutions in Latin America were the key elements of a world wide network of laboratories that received, on a competitive basis, financial support for projects in line with the priorities established. It is presented the time line of the different milestones that were answering successively and logically the outstanding scientific questions identified by the Scientific Working Group in 1978 and that influenced the development and industrial production of practical solutions for diagnosis of the infection and disease control}, Comment = {pdf ok }, File = {Moncayo2003.pdf:Moncayo2003.pdf:PDF;Moncayo2003.pdf:Documents/these/bibliographie/articles_chagas/Moncayo2003.pdf:PDF}, Keywords = {Chagas disease - Trypanosoma cruzi infection - control - interruption of transmission}, Owner = {Corentin}, Timestamp = {2006.10.16} }
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Description: application/vnd.oasis.opendocument.text
UniformRequirementStyle.jstyle
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