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\n  \n 2021\n \n \n (1)\n \n \n
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\n \n\n \n \n \n \n \n \n Comparison of the quantitative DiaSorin Liaison antigen test to RT-PCR for the diagnosis of COVID-19 in symptomatic and asymptomatic outpatients.\n \n \n \n \n\n\n \n Lefever, S.; Indevuyst, C.; Cuypers, L.; Dewaele, K.; Yin, N.; Cotton, F.; Padalko, E.; Oyaert, M.; Descy, J.; Cavalier, E.; Van Ranst, M.; André, E.; Lagrou, K.; and Vermeersch, P.\n\n\n \n\n\n\n Journal of Clinical Microbiology, (April). 2021.\n \n\n\n\n
\n\n\n\n \n \n \"ComparisonPaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@article{\n title = {Comparison of the quantitative DiaSorin Liaison antigen test to RT-PCR for the diagnosis of COVID-19 in symptomatic and asymptomatic outpatients},\n type = {article},\n year = {2021},\n id = {9637c329-7283-3740-9575-6750519267c7},\n created = {2021-05-05T08:00:25.152Z},\n file_attached = {true},\n profile_id = {941c2fd4-a583-308f-aea6-f6aaaa4aba4e},\n group_id = {fe056d04-cec3-35f3-b027-6e1c1824257d},\n last_modified = {2021-05-05T08:00:30.520Z},\n read = {false},\n starred = {false},\n authored = {false},\n confirmed = {true},\n hidden = {false},\n private_publication = {false},\n bibtype = {article},\n author = {Lefever, Stefanie and Indevuyst, Christophe and Cuypers, Lize and Dewaele, Klaas and Yin, Nicolas and Cotton, Frédéric and Padalko, Elizaveta and Oyaert, Matthijs and Descy, Julie and Cavalier, Etienne and Van Ranst, Marc and André, Emmanuel and Lagrou, Katrien and Vermeersch, Pieter},\n doi = {10.1128/jcm.00374-21},\n journal = {Journal of Clinical Microbiology},\n number = {April}\n}
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\n  \n 2014\n \n \n (1)\n \n \n
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\n \n\n \n \n \n \n \n \n Recommendations for the laboratory-based detection of Chlamydia trachomatis and Neisseria gonorrhoeae--2014.\n \n \n \n \n\n\n \n Report, M., W.\n\n\n \n\n\n\n MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports / Centers for Disease Control, 63: 1-19. 2014.\n \n\n\n\n
\n\n\n\n \n \n \"RecommendationsPaper\n  \n \n \n \"RecommendationsWebsite\n  \n \n\n \n\n \n link\n  \n \n\n bibtex\n \n\n \n  \n \n abstract \n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n \n\n\n\n
\n
@article{\n title = {Recommendations for the laboratory-based detection of Chlamydia trachomatis and Neisseria gonorrhoeae--2014.},\n type = {article},\n year = {2014},\n keywords = {Centers for Disease Control and Prevention (U.S.),Chlamydia Infections,Chlamydia Infections: diagnosis,Chlamydia trachomatis,Chlamydia trachomatis: isolation & purification,Clinical Laboratory Techniques,Clinical Laboratory Techniques: standards,Female,Gonorrhea,Gonorrhea: diagnosis,Guidelines as Topic,Humans,Male,Neisseria gonorrhoeae,Neisseria gonorrhoeae: isolation & purification,Nucleic Acid Amplification Techniques,United States},\n pages = {1-19},\n volume = {63},\n websites = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=4047970&tool=pmcentrez&rendertype=abstract},\n id = {20390322-997c-3b09-949e-1caf35a07743},\n created = {2015-03-20T14:10:26.000Z},\n file_attached = {true},\n profile_id = {f526f614-8bea-348f-be2d-22a3c99c128c},\n group_id = {fe056d04-cec3-35f3-b027-6e1c1824257d},\n last_modified = {2017-03-14T10:06:57.050Z},\n read = {false},\n starred = {false},\n authored = {false},\n confirmed = {true},\n hidden = {false},\n folder_uuids = {fd6603a8-e420-421c-be58-19e822ac4993},\n private_publication = {false},\n abstract = {This report updates CDC's 2002 recommendations regarding screening tests to detect Chlamydia trachomatis and Neisseria gonorrhoeae infections (CDC. Screening tests to detect Chlamydia trachomatis and Neisseria gonorrhoeae infections-2002. MMWR 2002;51[No. RR-15]) and provides new recommendations regarding optimal specimen types, the use of tests to detect rectal and oropharyngeal C. trachomatis and N. gonorrhoeae infections, and circumstances when supplemental testing is indicated. The recommendations in this report are intended for use by clinical laboratory directors, laboratory staff, clinicians, and disease control personnel who must choose among the multiple available tests, establish standard operating procedures for collecting and processing specimens, interpret test results for laboratory reporting, and counsel and treat patients. The performance of nucleic acid amplification tests (NAATs) with respect to overall sensitivity, specificity, and ease of specimen transport is better than that of any of the other tests available for the diagnosis of chlamydial and gonococcal infections. Laboratories should use NAATs to detect chlamydia and gonorrhea except in cases of child sexual assault involving boys and rectal and oropharyngeal infections in prepubescent girls and when evaluating a potential gonorrhea treatment failure, in which case culture and susceptibility testing might be required. NAATs that have been cleared by the Food and Drug Administration (FDA) for the detection of C. trachomatis and N. gonorrhoeae infections are recommended as screening or diagnostic tests because they have been evaluated in patients with and without symptoms. Maintaining the capability to culture for both N. gonorrhoeae and C. trachomatis in laboratories throughout the country is important because data are insufficient to recommend nonculture tests in cases of sexual assault in prepubescent boys and extragenital anatomic site exposure in prepubescent girls. N. gonorrhoeae culture is required to evaluate suspected cases of gonorrhea treatment failure and to monitor developing resistance to current treatment regimens. Chlamydia culture also should be maintained in some laboratories to monitor future changes in antibiotic susceptibility and to support surveillance and research activities such as detection of lymphogranuloma venereum or rare infections caused by variant or mutated C. trachomatis.},\n bibtype = {article},\n author = {Report, Mortality Weekly},\n journal = {MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports / Centers for Disease Control}\n}
\n
\n\n\n
\n This report updates CDC's 2002 recommendations regarding screening tests to detect Chlamydia trachomatis and Neisseria gonorrhoeae infections (CDC. Screening tests to detect Chlamydia trachomatis and Neisseria gonorrhoeae infections-2002. MMWR 2002;51[No. RR-15]) and provides new recommendations regarding optimal specimen types, the use of tests to detect rectal and oropharyngeal C. trachomatis and N. gonorrhoeae infections, and circumstances when supplemental testing is indicated. The recommendations in this report are intended for use by clinical laboratory directors, laboratory staff, clinicians, and disease control personnel who must choose among the multiple available tests, establish standard operating procedures for collecting and processing specimens, interpret test results for laboratory reporting, and counsel and treat patients. The performance of nucleic acid amplification tests (NAATs) with respect to overall sensitivity, specificity, and ease of specimen transport is better than that of any of the other tests available for the diagnosis of chlamydial and gonococcal infections. Laboratories should use NAATs to detect chlamydia and gonorrhea except in cases of child sexual assault involving boys and rectal and oropharyngeal infections in prepubescent girls and when evaluating a potential gonorrhea treatment failure, in which case culture and susceptibility testing might be required. NAATs that have been cleared by the Food and Drug Administration (FDA) for the detection of C. trachomatis and N. gonorrhoeae infections are recommended as screening or diagnostic tests because they have been evaluated in patients with and without symptoms. Maintaining the capability to culture for both N. gonorrhoeae and C. trachomatis in laboratories throughout the country is important because data are insufficient to recommend nonculture tests in cases of sexual assault in prepubescent boys and extragenital anatomic site exposure in prepubescent girls. N. gonorrhoeae culture is required to evaluate suspected cases of gonorrhea treatment failure and to monitor developing resistance to current treatment regimens. Chlamydia culture also should be maintained in some laboratories to monitor future changes in antibiotic susceptibility and to support surveillance and research activities such as detection of lymphogranuloma venereum or rare infections caused by variant or mutated C. trachomatis.\n
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\n  \n 2012\n \n \n (2)\n \n \n
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\n \n\n \n \n \n \n \n \n Management of Helicobacter pylori infection--the Maastricht IV/ Florence Consensus Report.\n \n \n \n \n\n\n \n Malfertheiner, P.; Megraud, F.; O'Morain, C., A.; Atherton, J.; Axon, A., T., R.; Bazzoli, F.; Gensini, G., F.; Gisbert, J., P.; Graham, D., Y.; Rokkas, T.; El-Omar, E., M.; and Kuipers, E., J.\n\n\n \n\n\n\n 2012.\n \n\n\n\n
\n\n\n\n \n \n \"ManagementPaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n  \n \n abstract \n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
\n
@misc{\n title = {Management of Helicobacter pylori infection--the Maastricht IV/ Florence Consensus Report},\n type = {misc},\n year = {2012},\n source = {Gut},\n pages = {646-664},\n volume = {61},\n id = {c49df7e4-00d4-32a8-89fa-34b3a84a2e75},\n created = {2015-03-20T14:37:12.000Z},\n file_attached = {true},\n profile_id = {f526f614-8bea-348f-be2d-22a3c99c128c},\n group_id = {fe056d04-cec3-35f3-b027-6e1c1824257d},\n last_modified = {2017-03-14T10:06:57.050Z},\n read = {false},\n starred = {false},\n authored = {false},\n confirmed = {true},\n hidden = {false},\n folder_uuids = {be9b35e3-9947-45f4-a991-76338b019f9e},\n private_publication = {false},\n abstract = {Management of Helicobacter pylori infection is evolving and in this 4th edition of the Maastricht consensus report aspects related to the clinical role of H pylori were looked at again in 2010. In the 4th Maastricht/Florence Consensus Conference 44 experts from 24 countries took active part and examined key clinical aspects in three subdivided workshops: (1) Indications and contraindications for diagnosis and treatment, focusing on dyspepsia, non-steroidal anti-inflammatory drugs or aspirin use, gastro-oesophageal reflux disease and extraintestinal manifestations of the infection. (2) Diagnostic tests and treatment of infection. (3) Prevention of gastric cancer and other complications. The results of the individual workshops were submitted to a final consensus voting to all participants. Recommendations are provided on the basis of the best current evidence and plausibility to guide doctors involved in the management of this infection associated with various clinical conditions.},\n bibtype = {misc},\n author = {Malfertheiner, P. and Megraud, F. and O'Morain, C. A. and Atherton, J. and Axon, A. T. R. and Bazzoli, F. and Gensini, G. F. and Gisbert, J. P. and Graham, D. Y. and Rokkas, T. and El-Omar, E. M. and Kuipers, E. J.},\n doi = {10.1136/gutjnl-2012-302084}\n}
\n
\n\n\n
\n Management of Helicobacter pylori infection is evolving and in this 4th edition of the Maastricht consensus report aspects related to the clinical role of H pylori were looked at again in 2010. In the 4th Maastricht/Florence Consensus Conference 44 experts from 24 countries took active part and examined key clinical aspects in three subdivided workshops: (1) Indications and contraindications for diagnosis and treatment, focusing on dyspepsia, non-steroidal anti-inflammatory drugs or aspirin use, gastro-oesophageal reflux disease and extraintestinal manifestations of the infection. (2) Diagnostic tests and treatment of infection. (3) Prevention of gastric cancer and other complications. The results of the individual workshops were submitted to a final consensus voting to all participants. Recommendations are provided on the basis of the best current evidence and plausibility to guide doctors involved in the management of this infection associated with various clinical conditions.\n
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\n \n\n \n \n \n \n \n \n Bed Bugs: Clinical Relevance and Control Options.\n \n \n \n \n\n\n \n Doggett, S., L.; Dwyer, D., E.; Penas, P., F.; and Russell, R., C.\n\n\n \n\n\n\n Clinical Microbiology Reviews, 25(1): 164-192. 2012.\n \n\n\n\n
\n\n\n\n \n \n \"BedPaper\n  \n \n \n \"BedWebsite\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
\n
@article{\n title = {Bed Bugs: Clinical Relevance and Control Options},\n type = {article},\n year = {2012},\n pages = {164-192},\n volume = {25},\n websites = {http://cmr.asm.org/cgi/doi/10.1128/CMR.05015-11},\n id = {9732c8c0-6a87-3b6b-8df4-566ee5f82c6e},\n created = {2015-10-21T13:17:05.000Z},\n file_attached = {true},\n profile_id = {f526f614-8bea-348f-be2d-22a3c99c128c},\n group_id = {fe056d04-cec3-35f3-b027-6e1c1824257d},\n last_modified = {2017-03-14T10:06:57.050Z},\n read = {false},\n starred = {false},\n authored = {false},\n confirmed = {true},\n hidden = {false},\n folder_uuids = {7be70d4d-2dc3-4e64-934a-595f8c3c0912},\n private_publication = {false},\n bibtype = {article},\n author = {Doggett, S. L. and Dwyer, D. E. and Penas, P. F. and Russell, R. C.},\n doi = {10.1128/CMR.05015-11},\n journal = {Clinical Microbiology Reviews},\n number = {1}\n}
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