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Matthew J. Stuckey, Bruno B. Chomel, Eloi Claret de Fleurieu, et al. Comparative Immunology, Microbiology and Infectious Diseases 55 20 (2017) https://doi.org/10.1016/j.cimid.2017.09.001
Clinical Research and Practice
Joanna Brydak-Godowska, Dorota Kopacz, Piotr K. Borkowski, et al. Advances in Experimental Medicine and Biology, Clinical Research and Practice 1020 33 (2017) https://doi.org/10.1007/5584_2017_19
Bartonella Infection in Hematophagous, Insectivorous, and Phytophagous Bat Populations of Central Mexico and the Yucatan Peninsula
Matthew J. Stuckey, Bruno B. Chomel, Cirani Obregón-Morales, et al. The American Journal of Tropical Medicine and Hygiene 97(2) 413 (2017) https://doi.org/10.4269/ajtmh.16-0680
Bartonella species pathogenic for humans infect pets, free-ranging wild mammals and their ectoparasites in the Caatinga biome, Northeastern Brazil: a serological and molecular study
Mariana Campos Fontalvo, Alexsandra Rodrigues de Mendonça Favacho, Andreina de Carvalho Araujo, et al. The Brazilian Journal of Infectious Diseases 21(3) 290 (2017) https://doi.org/10.1016/j.bjid.2017.02.002
Isolation of Bartonella henselae and Two New Bartonella Subspecies, Bartonella koehlerae Subspecies boulouisii subsp. nov. and Bartonella koehlerae Subspecies bothieri subsp. nov. from Free-Ranging Californian Mountain Lions and Bobcats
Isolation ofBartonella henselae, Bartonella koehleraesubsp.koehlerae, Bartonella koehleraesubsp.bothieriand a new subspecies ofB. koehleraefrom free-ranging lions (Panthera leo) from South Africa, cheetahs (Acinonyx jubatus) from Namibia and captive cheetahs from California
BartonellaSpecies Identified in Rodent and Feline Hosts from Island and Mainland Western Australia
Narelle A. Dybing, Caroline Jacobson, Peter Irwin, Dave Algar and Peter J. Adams Vector-Borne and Zoonotic Diseases 16(4) 238 (2016) https://doi.org/10.1089/vbz.2015.1902
Bacterial Zoonoses Transmitted by Household Pets: State-of-the-Art and Future Perspectives for Targeted Research and Policy Actions
Molecular identity of cat fleas (Ctenocephalides felis) from cats in Georgia, USA carrying Bartonella clarridgeiae, Bartonella henselae and Rickettsia sp. RF2125
BartonellaSpecies and Trombiculid Mites of Rats from the Mekong Delta of Vietnam
Hoang Kim Loan, Nguyen Van Cuong, Ratree Takhampunya, et al. Vector-Borne and Zoonotic Diseases 15(1) 40 (2015) https://doi.org/10.1089/vbz.2014.1604
Molecular screening of Ctenocephalides felis fleas collected from stray cats in the Jerusalem District, Israel, for Bartonella spp., Rickettsia spp. and Coxiella burnetii
Bartonellaspp. Infections in Rodents of Cambodia, Lao PDR, and Thailand: Identifying Risky Habitats
Tawisa Jiyipong, Serge Morand, Sathaporn Jittapalapong and Jean-Marc Rolain Vector-Borne and Zoonotic Diseases 15(1) 48 (2015) https://doi.org/10.1089/vbz.2014.1621
The efficacy of a selamectin (Stronghold®) spot on treatment in the prevention of Bartonella henselae transmission by Ctenocephalides felis in cats, using a new high-challenge model
Molecular detection of Bartonella clarridgeiae in domestic cats from Midwest Brazil
Ísis Assis Braga, Ingrid Savino de Oliveira Dias, Cristiane Silva Chitarra, Alexandre Mendes Amude and Daniel Moura Aguiar The Brazilian Journal of Infectious Diseases 19(4) 451 (2015) https://doi.org/10.1016/j.bjid.2015.05.002
Bartonella spp. Bacteremia in Blood Donors from Campinas, Brazil
Luiza Helena Urso Pitassi, Pedro Paulo Vissotto de Paiva Diniz, Diana Gerardi Scorpio, et al. PLOS Neglected Tropical Diseases 9(1) e0003467 (2015) https://doi.org/10.1371/journal.pntd.0003467
Prevalence of Rickettsia
and Bartonella
species in Spanish cats and their fleas
María Jesús Gracia, José Miguel Marcén, Rocio Pinal, Carlos Calvete and Daniel Rodes Journal of Vector Ecology 40(2) 233 (2015) https://doi.org/10.1111/jvec.12159
Did Bartonella henselae contribute to the deaths of two veterinarians?
A Translocated Effector Required for Bartonella Dissemination from Derma to Blood Safeguards Migratory Host Cells from Damage by Co-translocated Effectors
Bartonellaspp. Exposure in Northern and Southern Sea Otters in Alaska and California
Sebastian E. Carrasco, Bruno B. Chomel, Verena A. Gill, et al. Vector-Borne and Zoonotic Diseases 14(12) 831 (2014) https://doi.org/10.1089/vbz.2014.1612
MULTIPLEX SYBR® GREEN-REAL TIME PCR (qPCR) ASSAY FOR THE DETECTION AND DIFFERENTIATION OF Bartonella henselae AND Bartonella clarridgeiae IN CATS
Rodrigo Staggemeier, Diogo André Pilger, Fernando Rosado Spilki and Vlademir Vicente Cantarelli Revista do Instituto de Medicina Tropical de São Paulo 56(2) 93 (2014) https://doi.org/10.1590/S0036-46652014000200001
Bartonella and Toxoplasma Infections in Stray Cats from Iraq
Alexandra D. Switzer, Rickie W. Kasten, Philip H. Kass, et al. The American Journal of Tropical Medicine and Hygiene 89(6) 1219 (2013) https://doi.org/10.4269/ajtmh.13-0353
Experimental treatment of dog lice infestation in interior Alaska wolf packs
Craig L. Gardner, Kimberlee B. Beckmen, Nathan J. Pamperin and Patricia Del Vecchio The Journal of Wildlife Management 77(3) 626 (2013) https://doi.org/10.1002/jwmg.495
Fleas infesting pets in the era of emerging extra-intestinal nematodes
Serial Testing from a 3-Day Collection Period by Use of the Bartonella Alphaproteobacteria Growth Medium Platform May Enhance the Sensitivity of Bartonella Species Detection in Bacteremic Human Patients
Elizabeth L. Pultorak, Ricardo G. Maggi, Patricia E. Mascarelli and Edward B. Breitschwerdt Journal of Clinical Microbiology 51(6) 1673 (2013) https://doi.org/10.1128/JCM.00123-13
A Probabilistic Model in Cross-Sectional Studies for Identifying Interactions between Two Persistent Vector-Borne Pathogens in Reservoir Populations
Bartonella henselae bacteremia in a mother and son potentially associated with tick exposure
Ricardo G Maggi, Marna Ericson, Patricia E Mascarelli, Julie M Bradley and Edward B Breitschwerdt Parasites & Vectors 6(1) (2013) https://doi.org/10.1186/1756-3305-6-101
Ctenocephalides felis an in vitro potential vector for five Bartonella species
Emilie Bouhsira, Yann Ferrandez, MaFeng Liu, et al. Comparative Immunology, Microbiology and Infectious Diseases 36(2) 105 (2013) https://doi.org/10.1016/j.cimid.2012.10.004
BartonellaPrevalence and Genetic Diversity in Small Mammals from Ethiopia
Detection of Bartonella henselae DNA in clinical samples including peripheral blood of immune competent and immune compromised patients by three nested amplifications
Karina Hatamoto Kawasato, Léa Campos de Oliveira, Paulo Eduardo Neves Ferreira Velho, et al. Revista do Instituto de Medicina Tropical de São Paulo 55(1) 1 (2013) https://doi.org/10.1590/S0036-46652013000100001
Bartonellainfection in urban and rural dogs from the tropics: Brazil, Colombia, Sri Lanka and Vietnam
Assessment of Persistence of Bartonella henselae in Ctenocephalides felis
Emilie Bouhsira, Michel Franc, Henri-Jean Boulouis, et al. Applied and Environmental Microbiology 79(23) 7439 (2013) https://doi.org/10.1128/AEM.02598-13
Cat-scratch disease in Northern Italy: atypical clinical manifestations in humans and prevalence of Bartonella infection in cats
E. Brunetti, M. Fabbi, G. Ferraioli, et al. European Journal of Clinical Microbiology & Infectious Diseases 32(4) 531 (2013) https://doi.org/10.1007/s10096-012-1769-5
Bartonella Species Infection in Cats
Maria Grazia Pennisi, Fulvio Marsilio, Katrin Hartmann, Albert Lloret, Diane Addie, Sándor Belák, Corine Boucraut-Baralon, Herman Egberink, Tadeusz Frymus, Tim Gruffydd-Jones, Margaret J Hosie, Hans Lutz, Karin Möstl, Alan D Radford, Etienne Thiry, Uwe Truyen and Marian C Horzinek Journal of Feline Medicine and Surgery 15(7) 563 (2013) https://doi.org/10.1177/1098612X13489214
Rats, Cities, People, and Pathogens: A Systematic Review and Narrative Synthesis of Literature Regarding the Ecology of Rat-Associated Zoonoses in Urban Centers
Chelsea G. Himsworth, Kirbee L. Parsons, Claire Jardine and David M. Patrick Vector-Borne and Zoonotic Diseases 13(6) 349 (2013) https://doi.org/10.1089/vbz.2012.1195
Evolutionary history of rat‐borne Bartonella: the importance of commensal rats in the dissemination of bacterial infections globally
David T. S. Hayman, Katherine D. McDonald and Michael Y. Kosoy Ecology and Evolution 3(10) 3195 (2013) https://doi.org/10.1002/ece3.702
Bartonella Infections in Deer Keds (Lipoptena cervi) and Moose (Alces alces) in Norway
Small Indian mongooses and masked palm civets serve as new reservoirs of Bartonella henselae and potential sources of infection for humans
S. Sato, H. Kabeya, Y. Shigematsu, H. Sentsui, Y. Une, M. Minami, K. Murata, G. Ogura and S. Maruyama Clinical Microbiology and Infection 19(12) 1181 (2013) https://doi.org/10.1111/1469-0691.12164
Bilateral Bartonella henselae neuroretinitis with stellate maculopathy in a 6-year-old boy
Seroepidemiology ofBartonellaInfection in Gray Foxes from Texas
Jonathan D. Schaefer, Guy M. Moore, Michael S. Namekata, Rick W. Kasten and Bruno B. Chomel Vector-Borne and Zoonotic Diseases 12(5) 428 (2012) https://doi.org/10.1089/vbz.2011.0805
Bartonella Species Antibodies and Hyperglobulinemia in Privately Owned Cats
Bartonella spp. in human and animal populations in Gauteng, South Africa, from 2007 to 2009
Anastasia N. Trataris, Jennifer Rossouw, Lorraine Arntzen, Allan Karstaedt and John Frean Onderstepoort J Vet Res 79(2) (2012) https://doi.org/10.4102/ojvr.v79i2.452
Bartonellaspp. Bacteremia and Rheumatic Symptoms in Patients from Lyme Disease–endemic Region
Questing Ticks in Suburban Forest Are Infected by at Least Six Tick-Borne Pathogens
Caroline Reis, Martine Cote, Richard E.L. Paul and Sarah Bonnet Vector-Borne and Zoonotic Diseases 11(7) 907 (2011) https://doi.org/10.1089/vbz.2010.0103
Isolation or detection of Bartonella vinsonii subspecies berkhoffii and Bartonella rochalimae in the endangered island foxes (Urocyon littoralis)
Jonathan D. Schaefer, Rickie W. Kasten, Timothy J. Coonan, Deana L. Clifford and Bruno B. Chomel Veterinary Microbiology 154(1-2) 135 (2011) https://doi.org/10.1016/j.vetmic.2011.06.031
Manual of Clinical Microbiology
Ricardo G. Maggi, Volkhard A.J. Kempf, Bruno B. Chomel and Edward B. Breitschwerdt Manual of Clinical Microbiology 786 (2011) https://doi.org/10.1128/9781555816728.ch46
Multilocus Sequence Typing of Bartonella henselae in the United Kingdom Indicates that Only a Few, Uncommon Sequence Types Are Associated with Zoonotic Disease
Gemma L. Chaloner, Timothy G. Harrison, Karen P. Coyne, David M. Aanensen and Richard J. Birtles Journal of Clinical Microbiology 49(6) 2132 (2011) https://doi.org/10.1128/JCM.00275-11
Bartonella henselae infection and its effects on human health