Evidence of Bartonella sp. in questing adult and nymphal Ixodes ricinus ticks from France and co-infection with Borrelia burgdorferi sensu lato and Babesia sp.
Vet. Res., 36 1 (2005) 79-87
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https://doi.org/10.3389/fpubh.2014.00251
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https://doi.org/10.1186/1297-9716-45-65
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https://doi.org/10.1089/vbz.2011.0933
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https://doi.org/10.1007/s15010-013-0526-8
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https://doi.org/10.1371/journal.pone.0066167
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R Welc-Falęciak, A Bajer, A Paziewska-Harris, A Baumann-Popczyk and E SińskiAdvances in Medical Sciences 57 (2) 364 (2012)
https://doi.org/10.2478/v10039-012-0023-9
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https://doi.org/10.1089/vbz.2011.0807
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https://doi.org/10.1128/JB.06244-11
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Olga Katargina, Julia Geller, Veera Vasilenko, et al.Vector-Borne and Zoonotic Diseases 11 (7) 923 (2011)
https://doi.org/10.1089/vbz.2010.0199
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https://doi.org/10.1089/vbz.2010.0103
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Sabine Schorn, Kurt Pfister, Holger Reulen, Monia Mahling and Cornelia SilaghiParasites & Vectors 4 (1) (2011)
https://doi.org/10.1186/1756-3305-4-135
Bartonella species and their ectoparasites: Selective host adaptation or strain selection between the vector and the mammalian host?
Yi-Lun Tsai, Chao-Chin Chang, Shih-Te Chuang and Bruno B. ChomelComparative Immunology, Microbiology and Infectious Diseases 34 (4) 299 (2011)
https://doi.org/10.1016/j.cimid.2011.04.005
259 (2011)
https://doi.org/10.1007/978-3-642-21396-0_14
Prevalence of Bartonella henselae and Borrelia burgdorferi Sensu Lato DNA in Ixodes ricinus Ticks in Europe
Florian Dietrich, Thomas Schmidgen, Ricardo G. Maggi, et al.Applied and Environmental Microbiology 76 (5) 1395 (2010)
https://doi.org/10.1128/AEM.02788-09
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Anke Hildebrandt, Katharina Pauliks, Svea Sachse and Eberhard StraubeVector-Borne and Zoonotic Diseases 10 (9) 831 (2010)
https://doi.org/10.1089/vbz.2009.0202
Prevalence and Seasonality of Tick-Borne Pathogens in Questing Ixodes ricinus Ticks from Luxembourg
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https://doi.org/10.1128/AEM.03061-09
Prevalence of Five Pathogenic Agents in QuestingIxodes ricinusTicks from Western France
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https://doi.org/10.1089/vbz.2009.0066
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https://doi.org/10.3201/eid1603.081685
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https://doi.org/10.3201/eid1603.091685
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https://doi.org/10.1007/s00508-009-1281-9
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https://doi.org/10.1111/j.1469-0691.2008.02196.x
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https://doi.org/10.1089/vbz.2008.0132
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https://doi.org/10.1016/j.vetpar.2009.03.028
Neuroretinitis secondary to concurrent infection with cat scratch disease and lyme disease
P K Gupta, R Patel and M T BhattiEye 23 (7) 1607 (2009)
https://doi.org/10.1038/eye.2008.288
Bartonella: emerging pathogen or emerging awareness?
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https://doi.org/10.1016/j.ijid.2008.04.002
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https://doi.org/10.1111/j.1365-2915.2008.00748.x
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https://doi.org/10.3201/eid1407.071110
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https://doi.org/10.1128/JCM.00832-08
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https://doi.org/10.1111/j.1365-2915.2008.00713.x
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https://doi.org/10.1371/journal.ppat.0040007
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https://doi.org/10.1128/AEM.00035-08
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F. T. Just, J. Gilles, I. Pradel, et al.Zoonoses and Public Health 55 (8-10) 514 (2008)
https://doi.org/10.1111/j.1863-2378.2008.01131.x
Ticks
S. R. Telford and H. K. GoethertTicks 344 (2008)
https://doi.org/10.1017/CBO9780511551802.017
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B. Skotarczak, M. Adamska, M. Sawczuk, A. Maciejewska, B. Wodecka and A. RymaszewskaVeterinární medicína 53 (12) 668 (2008)
https://doi.org/10.17221/1975-VETMED
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https://doi.org/10.1016/S0001-4079(19)32978-4
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