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LIFE CYCLE OF HEPATOZOON CANIS (APICOMPLEXA: ADELEORINA: HEPATOZOIDAE) IN THE TICK RHIPICEPHALUS SANGUINEUS AND DOMESTIC DOG (CANIS FAMILIARIS)

https://doi.org/10.1645/ge-494r.1
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/bf00329601openalex-snapshot
Cycle biologique d'Hepatozoon domerguei; discussion sur les caract�res fondamentaux d'un cycle de Coccidie
inferredcites →https://doi.org/10.1007/bf00346576openalex-snapshot
Hepatozoon canis: The prevalence of antibodies and gametocytes in dogs in Israel
inferredcites →https://doi.org/10.1007/bf00931635openalex-snapshot
Life cycle ofHepatozoon mehlhorni. sp. nov. in the viperEchis carinatus and the mosquitoCulex pipiens
inferredcites →https://doi.org/10.1007/bf00933003openalex-snapshot
The development ofHepatozoon sipedon sp. nov. (Apicomplexa: Adeleina: Hepatozoidae) in its natural host, the Northern water snake (Nerodia sipedon sipedon), in the culicine vectorsCulex pipiens andC. territans, and in an intermediate host, the Northern leopard frog (Rana pipiens)
inferredcites →https://doi.org/10.1016/0035-9203(81)90052-3openalex-snapshot
Development of Hepatozoon erhardovae Krampitz, 1964 (Protozoa: Haemogregarinidae) in experimental mammalian and arthropod hosts. II. Sexual development in fleas and sporozoite indices in xenodiagnosis
inferredcites →https://doi.org/10.1016/0304-4017(84)90038-4openalex-snapshot
Experimental transmission of the texas strain of Hepatozoon canis
inferredcites →https://doi.org/10.1016/0304-4017(85)90101-3openalex-snapshot
The incidence of canine haematozoa in peninsular Malaysia
inferredcites →https://doi.org/10.1016/0304-4017(92)90055-eopenalex-snapshot
Concurrent Hepatozoon canis and Toxoplasma gondii infections in a dog
inferredcites →https://doi.org/10.1016/0304-4017(93)90009-copenalex-snapshot
Ultrastructure of Hepatozoon canis in the dog
inferredcites →https://doi.org/10.1016/j.vetpar.2005.05.066openalex-snapshot
Diagnosis of Hepatozoon spp. in Amblyomma ovale and its experimental transmission in domestic dogs in Brazil
inferredcites →https://doi.org/10.1016/j.wem.2013.06.013openalex-snapshot
Transactions of the Royal Society of Tropical Medicine and Hygiene
inferredcites →https://doi.org/10.1016/s0304-4017(00)00378-2openalex-snapshot
Hepatozoon canis infection associated with dog ticks of rural areas of Rio de Janeiro State, Brazil
inferredcites →https://doi.org/10.1016/s0304-4017(96)01152-1openalex-snapshot
Hepatozoon canis infection in a litter of Dalmatian dogs
inferredcites →https://doi.org/10.1016/s0304-4017(97)00160-xopenalex-snapshot
Antibody response to Hepatozoon canis in experimentally infected dogs
inferredcites →https://doi.org/10.1016/s0304-4017(98)00189-7openalex-snapshot
Experimental transmission of Hepatozoon americanum Vincent-Johnson et al., 1997 to dogs by the Gulf Coast tick, Amblyomma maculatum Koch
inferredcites →https://doi.org/10.1016/s0304-4017(99)00029-1openalex-snapshot
Canine hepatozoonosis: comparison of lesions and parasites in skeletal muscle of dogs experimentally or naturally infected with Hepatozoon americanum
inferredcites →https://doi.org/10.1017/s0031182000002730openalex-snapshot
Oriental sore in Bagdad, together with observations on a gregarine in Stegomyia fasciata, the haemogregarine of dogs and the flagellates of house flies
inferredcites →https://doi.org/10.1051/parasite/1973481011openalex-snapshot
Hepatozoon mauritanicum (Et. et Ed. Sergent, 1904) n. comb., parasite de Testudo graeca : redescription de la sporogonie chez Hyalomma aegyptium et de la schizogonie tissulaire d’après le matériel d’E. Brumpt
inferredcites →https://doi.org/10.1051/parasite/1995022141openalex-snapshot
Life history and ultrastructure ofEimeria bufomarinin.sp. (Apicomplexa: Eimeriidae) of the giant toad, Bufo marinus (Amphibia: Anura) from Amazonian Brazil
inferredcites →https://doi.org/10.1051/parasite/1997042141openalex-snapshot
Ultrastructural features of the gametogenic and sporogonic development ofHepatozoon sipedon(Apicomplexa: Adeleorina) The applicability of ultrastructural data in differentiating amongHepatozoonspecies
inferredcites →https://doi.org/10.1051/parasite/200209117openalex-snapshot
Hepatozoon kisraen. sp. infecting the lizardAgama stelliois transmitted by the tickHyalommacf.aegyptium
inferredcites →https://doi.org/10.1080/00034983.1973.11686907openalex-snapshot
A comparison of the life cycles ofToxoplasmaandHepatozoon, with reference to the general phenomenon and the role of cyst formation in the Coccidia
inferredcites →https://doi.org/10.1093/infdis/121.3.339openalex-snapshot
Scanning-Beam Electron Microscopy of Selected Microorganisms
inferredcites →https://doi.org/10.1111/j.1439-0450.1988.tb00478.xopenalex-snapshot
Experimental Treatment of Hepatozoon Infections with the Anticoccidial Agent Toltrazuril
inferredcites →https://doi.org/10.1111/j.1439-0450.1997.tb00957.xopenalex-snapshot
Ultrastructural Findings in Natural Canine Hepatozoonosis
inferredcites →https://doi.org/10.1111/j.1550-7408.1988.tb04080.xopenalex-snapshot
Ultrastructural Features of the Apical Complex, Pellicle, and Membranes Investing the Gamonts of Haemogregarina magna (Apicomplexa: Adeleina)1
inferredcites →https://doi.org/10.1111/j.1550-7408.1993.tb04918.xopenalex-snapshot
Gametogenesis and Sporogony of Hepatozoon Mocassini (Apicomplexa: Adeleina: Hepatozoidae) In an Experimental Mosquito Host, Aedes Aegypti
inferredcites →https://doi.org/10.1111/j.1550-7408.1998.tb05093.xopenalex-snapshot
Ultrastructural Features of Cystic and Merogonic Stages of Hepatozoon sipedon (Apicomplexa: Adeleorina) in Northern Leopard Frogs (Rana pipiens) and Northern Water Snakes (Nerodia sipedon) from Ontario, Canada
inferredcites →https://doi.org/10.1111/j.1748-5827.1983.tb00385.xopenalex-snapshot
Clinical and epidemiological studies on canine hepatozoonosis in Zaria, Nigeria
inferredcites →https://doi.org/10.1111/j.1939-1676.1997.tb00482.xopenalex-snapshot
Retrospective Case-Control Study of Hepatozoonosis in Dogs in Israel
inferredcites →https://doi.org/10.1128/cmr.16.4.688-697.2003openalex-snapshot
American Canine Hepatozoonosis
inferredcites →https://doi.org/10.1136/vr.137.20.518openalex-snapshot
Acute fatal hepatozoonosis in a puppy: histopathological and ultrastructural study
inferredcites →https://doi.org/10.1177/104063879400600127openalex-snapshot
Circulating Antibodies to Hepatozoon Canis Demonstrated by Immunofluorescence
inferredcites →https://doi.org/10.1292/jvms.53.1097openalex-snapshot
First Case of Hepatozoon canis Infection of a Dog in Japan.
inferredcites →https://doi.org/10.1292/jvms.55.867openalex-snapshot
Vertical Transmission of Hepatozoon canis in Dogs.
inferredcites →https://doi.org/10.1354/vp.37-3-225openalex-snapshot
Skeletal Lesions of Canine Hepatozoonosis Caused by Hepatozoon americanum
inferredcites →https://doi.org/10.1354/vp.42-6-788openalex-snapshot
Characterization of Stages of Hepatozoon americanum and of Parasitized Canine Host Cells
inferredcites →https://doi.org/10.1645/0022-3395(2001)087[0606:tohctd]2.0.co;2openalex-snapshot
Transmission ofHepatozoon canisto Dogs by Naturally-Fed or Percutaneously-InjectedRhipicephalus sanguineusTicks
inferredcites →https://doi.org/10.1645/0022-3395(2003)089[0379:mcohc]2.0.co;2openalex-snapshot
Monozoic Cysts of Hepatozoon canis
inferredcites →https://doi.org/10.2149/tmh1973.21.107openalex-snapshot
Fine structure of gamont of Hepatozoon canis.
inferredcites →https://doi.org/10.2307/3274829openalex-snapshot
Hepatozoon griseisciuri n. sp.; A New Species of Hepatozoon from the Grey Squirrel (Sciurus carolinensis Gmelin, 1788), with Studies on the Life Cycle
inferredcites →https://doi.org/10.2307/3276504openalex-snapshot
Hepatozoon balfouri (Laveran, 1905): Sporogonic Cycle, Pathogenesis, and Transmission by Mites to Jerboa Hosts
inferredcites →https://doi.org/10.2307/3276805openalex-snapshot
The Life History of Hepatozoon rarefaciens (Sambon and Seligmann, 1907) from Drymarchon corais (Colubridae), and Its Experimental Transfer to Constrictor constrictor (Boidae)
inferredcites →https://doi.org/10.2307/3277220openalex-snapshot
Hepatozoon fusifex sp. n., a Hemogregarine from Boa constrictor Producing Marked Morphological Changes in Infected Erythrocytes
inferredcites →https://doi.org/10.2307/3277842openalex-snapshot
Syngamy and Sporogony of Hepatozoon griseisciuri Clark, 1958 (Sporozoa: Haemogregarinidae), in Its Natural Vector, Haemogamasus reidi Ewing, 1925 (Acari:Mesostigmata)
inferredcites →https://doi.org/10.2307/3280710openalex-snapshot
Developmental Stages of Hepatozoon lygosomarum (Doré 1919) comb. n. (Protozoa: Haemogregarinidae), a Parasite of a New Zealand Skink, Leiolopisma nigriplantare
inferredcites →https://doi.org/10.2307/3283027openalex-snapshot
Tissue "Cysts" of Hepatozoon griseisciuri in the Grey Squirrel, Sciurus carolinensis: The Significance of These Cysts in Species of Hepatozoon
inferredcites →https://doi.org/10.2307/3283781openalex-snapshot
The Genus Hepatozoon (Apicomplexa: Adeleina)
inferredcites →https://doi.org/10.2307/3283922openalex-snapshot
The Life History, Ultrastructure, and Experimental Transmission of Hepatozoon catesbianae n. comb., an Apicomplexan Parasite of the Bullfrog, Rana catesbeiana and the Mosquito, Culex territans in Algonquin Park, Ontario
inferredcites →https://doi.org/10.2307/3284379openalex-snapshot
A New Hepatozoon Species from Dogs: Description of the Causative Agent of Canine Hepatozoonosis in North America
inferredcites →https://doi.org/10.2307/3285663openalex-snapshot
Sporogonic Development of Hepatozoon americanum (Apicomplexa) in Its Definitive Host, Amblyomma maculatum (Acarina)
inferredcites →https://doi.org/10.2460/javma.1995.206.12.1891openalex-snapshot
Hepatozoon canis infection in two dogs
inferredcites →https://doi.org/10.2460/javma.1997.210.07.916openalex-snapshot
Hepatozoonosis in dogs: 22 cases (1989-1994)
inferredcites →https://doi.org/10.7589/0090-3558-36.1.149openalex-snapshot
Naturally Occurring and Experimentally Transmitted Hepatozoon americanum in Coyotes from Oklahoma

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Molecular survey of tick-borne pathogens reveals a high prevalence and low genetic variability of Hepatozoon canis in free-ranging grey wolves (Canis lupus) in Germany
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inferred← citeshttps://doi.org/10.1016/j.vetpar.2007.10.017openalex-snapshot
Experimental transmission of Hepatozoon americanum to rodents
inferred← citeshttps://doi.org/10.1016/j.vetpar.2007.12.030openalex-snapshot
The brown dog tick, Rhipicephalus sanguineus (Latreille, 1806) (Acari: Ixodidae): From taxonomy to control
inferred← citeshttps://doi.org/10.1016/j.vetpar.2008.03.027openalex-snapshot
Diversity of Hepatozoon species in naturally infected dogs in the southern United States
inferred← citeshttps://doi.org/10.1016/j.vetpar.2008.06.027openalex-snapshot
Diagnosis of canine Hepatozoon spp. infection by quantitative PCR
inferred← citeshttps://doi.org/10.1016/j.vetpar.2009.05.009openalex-snapshot
Acquisition and transmission of Hepatozoon canis (Apicomplexa: Hepatozoidae) by the tick Amblyomma ovale (Acari: Ixodidae)
inferred← citeshttps://doi.org/10.1016/j.vetpar.2009.05.028openalex-snapshot
Experimental transmission of Hepatozoon americanum to New Zealand White rabbits (Oryctolagus cuniculus) and infectivity of cystozoites for a dog
inferred← citeshttps://doi.org/10.1016/j.vetpar.2011.01.044openalex-snapshot
Oocysts of Hepatozoon canis in Rhipicephalus (Boophilus) microplus collected from a naturally infected dog
inferred← citeshttps://doi.org/10.1016/j.vetpar.2011.03.042openalex-snapshot
Efficacy of a novel topical combination of fipronil, amitraz and (S)-methoprene for treatment and control of induced infestations of brown dog ticks (Rhipicephalus sanguineus) on dogs
inferred← citeshttps://doi.org/10.1016/j.vetpar.2011.04.015openalex-snapshot
Perspectives on canine and feline hepatozoonosis
inferred← citeshttps://doi.org/10.1016/j.vetpar.2011.04.020openalex-snapshot
Canine vector-borne disease in travelled dogs in Germany—A retrospective evaluation of laboratory data from the years 2004–2008
inferred← citeshttps://doi.org/10.1016/j.vetpar.2011.11.006openalex-snapshot
Infection with a Hepatozoon sp. closely related to Hepatozoon felis in a wild Pampas gray fox (Lycalopex – Pseudalopex – gymnocercus) co-infected with canine distemper virus
inferred← citeshttps://doi.org/10.1016/j.vetpar.2011.11.036openalex-snapshot
Molecular characterization of Hepatozoon spp. infection in endangered Indian wild felids and canids
inferred← citeshttps://doi.org/10.1016/j.vetpar.2013.02.017openalex-snapshot
Transstadial transmission of Hepatozoon canis from larvae to nymphs of Rhipicephalus sanguineus
inferred← citeshttps://doi.org/10.1016/j.vetpar.2013.12.007openalex-snapshot
First report of Angiostrongylus vasorum and Hepatozoon from a red fox (Vulpes vulpes) from West Virginia, USA
inferred← citeshttps://doi.org/10.1016/j.vetpar.2013.12.013openalex-snapshot
Failure of imidocarb dipropionate and toltrazuril/emodepside plus clindamycin in treating Hepatozoon canis infection
inferred← citeshttps://doi.org/10.1016/j.vetpar.2014.12.013openalex-snapshot
Canine vector-borne co-infections: Ehrlichia canis and Hepatozoon canis in the same host monocytes
inferred← citeshttps://doi.org/10.1016/j.vetpar.2021.109392openalex-snapshot
Ticks infesting dogs and cats in North America: Biology, geographic distribution, and pathogen transmission
inferred← citeshttps://doi.org/10.1016/j.vetpar.2025.110408openalex-snapshot
Hepatozoon infections in dogs and cats in USA: History, life cycle, and suggestions for uniform terminology for hepatozoonosis in endotherms and ectotherms
inferred← citeshttps://doi.org/10.1016/j.vprsr.2017.02.008openalex-snapshot
Hematological and epidemiological characterization of Hepatozoon canis infection in dogs from Buenos Aires, Argentina
inferred← citeshttps://doi.org/10.1016/j.vprsr.2023.100908openalex-snapshot
Morphological and molecular identification of the brown dog tick in Mexico
inferred← citeshttps://doi.org/10.1016/j.vprsr.2025.101233openalex-snapshot
Molecular detection of Hepatozoon spp. and Cytauxzoon felis in wild carnivorans and domestic dogs in southern Pantanal wetlands of Brazil with new host records
inferred← citeshttps://doi.org/10.1016/j.vprsr.2026.101501openalex-snapshot
Coinfection with Hepatozoon felis and feline coronavirus in a domestic cat from Russia: A case report
inferred← citeshttps://doi.org/10.1017/s0031182016002201openalex-snapshot
Detection and molecular identification of Hepatozoon canis and Babesia vogeli from domestic dogs in Palestine
inferred← citeshttps://doi.org/10.1017/s0031182016002316openalex-snapshot
Hepatozoon silvestris sp. nov.: morphological and molecular characterization of a new species of Hepatozoon (Adeleorina: Hepatozoidae) from the European wild cat (Felis silvestris silvestris)
inferred← citeshttps://doi.org/10.1017/s003118201600250xopenalex-snapshot
Rhipicephalus turanicus , a new vector of Hepatozoon canis
inferred← citeshttps://doi.org/10.1017/s0031182018001956openalex-snapshot
Hepatozoon milleri sp. nov. (Adeleorina: Hepatozoidae) in Akodon montensis (Rodentia: Cricetidae: Sigmodontinae) from southeastern Brazil
inferred← citeshttps://doi.org/10.1038/s41598-023-28346-0openalex-snapshot
Candidatus Neoehrlichia mikurensis and Hepatozoon sp. in voles (Microtus spp.): occurrence and evidence for vertical transmission
inferred← citeshttps://doi.org/10.1051/parasite/2013010openalex-snapshot
Arthropod-borne infections in travelled dogs in Europe
inferred← citeshttps://doi.org/10.1055/a-1266-8042openalex-snapshot
Der kleine Unbekannte – Hepatozoonose bei Hunden und Katzen
inferred← citeshttps://doi.org/10.1080/01647954.2021.2015437openalex-snapshot
Molecular investigation on transstadial/transovarial transmission of Hepatozoon canis in Rhipicephalus sanguineus sensu lato ticks
inferred← citeshttps://doi.org/10.1089/vbz.2009.0182openalex-snapshot
The First Report of Hepatozoon canis Identified in Vulpes vulpes and Ticks from Italy
inferred← citeshttps://doi.org/10.1089/vbz.2016.1963openalex-snapshot
A Review of Methods for Detection of Hepatozoon Infection in Carnivores and Arthropod Vectors
inferred← citeshttps://doi.org/10.1089/vbz.2023.0088openalex-snapshot
The Occurrence and Diversity of Tick-Borne Pathogens in Small Mammals from Serbia
inferred← citeshttps://doi.org/10.1093/jme/tjx050openalex-snapshot
Transstadial Transmission of Hepatozoon canis by Rhipicephalus sanguineus (Acari: Ixodidae) in Field Conditions
inferred← citeshttps://doi.org/10.1093/jme/tjy081openalex-snapshot
Detection of Hepatozoon canis in the Brown Dog Tick and Domestic Dogs in Peninsular Malaysia
inferred← citeshttps://doi.org/10.1111/j.1939-165x.2008.00080.xopenalex-snapshot
Hepatozoonosis in a dog with skeletal involvement and meningoencephalomyelitis
inferred← citeshttps://doi.org/10.1111/mve.12479openalex-snapshot
Prevalence and distribution of pathogen infection and permethrin resistance in tropical and temperate populations of Rhipicephalus sanguineus s.l. collected worldwide
inferred← citeshttps://doi.org/10.1111/tbed.14199openalex-snapshot
An epidemiological study in wild carnivores from Spanish Mediterranean ecosystems reveals association between Leishmania infantum, Babesia spp. and Hepatozoon spp. infection and new hosts for Hepatozoon martis, Hepatozoon canis and Sarcocystis spp.
inferred← citeshttps://doi.org/10.1111/vcp.12752openalex-snapshot
Hepatozoon canis infection causing a strong monocytosis with intra‐monocytic gamonts and leading to erroneous leukocyte determinations
inferred← citeshttps://doi.org/10.1136/vr.105087openalex-snapshot
Hepatozoon canis in three imported dogs: a new tickborne disease reaching the United Kingdom
inferred← citeshttps://doi.org/10.1139/cjz-2012-0241openalex-snapshot
Factors determining the in vitro emergence of sexual stages of Hepatozoon clamatae from erythrocytes of the Green Frog (Rana clamitans)
inferred← citeshttps://doi.org/10.1155/japr/5430576openalex-snapshot
First Evidence of Hepatozoon canis in Dogs With Clinical Signs in the North of Lima, Peru
inferred← citeshttps://doi.org/10.11606/t.10.2022.tde-25042022-082923openalex-snapshot
>b /b<
inferred← citeshttps://doi.org/10.1163/15685381-20191113openalex-snapshot
Molecular and morphological characterization of Hepatozoon spp. in Brazilian snakes
inferred← citeshttps://doi.org/10.1177/1098612x17691172openalex-snapshot
Minimum transmission time of Cytauxzoon felis by Amblyomma americanum to domestic cats in relation to duration of infestation, and investigation of ingestion of infected ticks as a potential route of transmission
inferred← citeshttps://doi.org/10.1186/1756-3305-2-s1-s5openalex-snapshot
New developments in canine hepatozoonosis in North America: a review
inferred← citeshttps://doi.org/10.1186/1756-3305-3-27openalex-snapshot
Canine babesiosis in northern Portugal and molecular characterization of vector-borne co-infections
inferred← citeshttps://doi.org/10.1186/1756-3305-4-55openalex-snapshot
Diagnosis of Hepatozoon canis in young dogs by cytology and PCR
inferred← citeshttps://doi.org/10.1186/1756-3305-5-98openalex-snapshot
Detection of Leishmania infantum DNA mainly in Rhipicephalus sanguineus male ticks removed from dogs living in endemic areas of canine leishmaniosis
inferred← citeshttps://doi.org/10.1186/1756-3305-6-102openalex-snapshot
Redescription of Hepatozoon felis (Apicomplexa: Hepatozoidae) based on phylogenetic analysis, tissue and blood form morphology, and possible transplacental transmission
inferred← citeshttps://doi.org/10.1186/1756-3305-7-113openalex-snapshot
Molecular and histopathological detection of Hepatozoon canis in red foxes (Vulpes vulpes) from Portugal
inferred← citeshttps://doi.org/10.1186/1756-3305-7-126openalex-snapshot
First report of Babesia gibsoni in Central America and survey for vector-borne infections in dogs from Nicaragua
inferred← citeshttps://doi.org/10.1186/1756-3305-7-303openalex-snapshot
First molecular evidence of Hepatozoon canis infection in red foxes and golden jackals from Hungary
inferred← citeshttps://doi.org/10.1186/s12917-024-04267-6openalex-snapshot
Surveillance of tick-borne pathogens in domestic dogs from Chad, Africa
inferred← citeshttps://doi.org/10.1186/s13071-015-0692-xopenalex-snapshot
A molecular survey of vector-borne pathogens in red foxes (Vulpes vulpes) from Bosnia and Herzegovina
inferred← citeshttps://doi.org/10.1186/s13071-017-2063-2openalex-snapshot
Prevalence study and risk factor analysis of selected bacterial, protozoal and viral, including vector-borne, pathogens in cats from Cyprus
inferred← citeshttps://doi.org/10.1186/s13071-018-2717-8openalex-snapshot
Association between canine leishmaniosis and Ehrlichia canis co-infection: a prospective case-control study
inferred← citeshttps://doi.org/10.1186/s13071-018-2775-yopenalex-snapshot
Endemic, exotic and novel apicomplexan parasites detected during a national study of ticks from companion animals in Australia
inferred← citeshttps://doi.org/10.1186/s13071-018-2992-4openalex-snapshot
Fatal infection with emerging apicomplexan parasite Hepatozoon silvestris in a domestic cat
inferred← citeshttps://doi.org/10.1186/s13071-019-3389-8openalex-snapshot
Molecular investigation of vector-borne parasitic infections in dogs in Northeast India
inferred← citeshttps://doi.org/10.1186/s13071-020-04051-zopenalex-snapshot
Detection of DNA of Babesia canis in tissues of laboratory rodents following oral inoculation with infected ticks
inferred← citeshttps://doi.org/10.1186/s13071-020-04057-7openalex-snapshot
Stray dogs in Nepal have high prevalence of vector-borne pathogens: a molecular survey
inferred← citeshttps://doi.org/10.1186/s13071-021-04779-2openalex-snapshot
Molecular investigation of bacterial and protozoal pathogens in ticks collected from different hosts in Turkey
inferred← citeshttps://doi.org/10.1186/s13071-022-05348-xopenalex-snapshot
Screening and phylogenetic characterization of tick-borne pathogens in a population of dogs and associated ticks in Egypt
inferred← citeshttps://doi.org/10.1186/s13071-022-05392-7openalex-snapshot
First evidence of vertical Hepatozoon canis transmission in dogs in Europe
inferred← citeshttps://doi.org/10.1186/s13071-022-05534-xopenalex-snapshot
First autochthonous clinical case of Hepatozoon silvestris in a domestic cat in Italy with unusual presentation
inferred← citeshttps://doi.org/10.1186/s13071-022-05626-8openalex-snapshot
Diversity of Hepatozoon species in wild mammals and ticks in Europe
inferred← citeshttps://doi.org/10.1186/s13071-023-05683-7openalex-snapshot
Apicomplexan haemoparasites in domestic cats in Romania
inferred← citeshttps://doi.org/10.1186/s13071-024-06154-3openalex-snapshot
Hepatozoon (Eucoccidiorida: Hepatozoidae) in wild mammals of the Americas: a systematic review
inferred← citeshttps://doi.org/10.1186/s13071-024-06326-1openalex-snapshot
First identification of Cytauxzoon manul in Eurasian lynx (Lynx lynx) in northwestern China
inferred← citeshttps://doi.org/10.1186/s13071-024-06572-3openalex-snapshot
The Rhipicephalus sanguineus group: updated list of species, geographical distribution, and vector competence
inferred← citeshttps://doi.org/10.1186/s13071-025-06777-0openalex-snapshot
Vector-borne pathogens in dogs from the Republic of Kosovo
inferred← citeshttps://doi.org/10.1186/s13071-025-06977-8openalex-snapshot
Hepatozoon infections in domestic and wild Carnivora: etiology, prevalence, clinical disease, diagnosis and treatment, and redescription of Hepatozoon silvestris, H. martis, and H. ursi
inferred← citeshttps://doi.org/10.1186/s13071-026-07405-1openalex-snapshot
Efficacy of Credelio Quattro™ chewable tablets containing lotilaner, moxidectin, pyrantel, and praziquantel against Ctenocephalides felis and Rhipicephalus sanguineus infestations on dogs
inferred← citeshttps://doi.org/10.1186/s40249-016-0106-0openalex-snapshot
Epidemiology of toxoplasmosis: role of the tick Haemaphysalis longicornis
inferred← citeshttps://doi.org/10.12935/jvma.78.e95openalex-snapshot
First Report of Hepatozoon canis Infection in a Dog from Chiba Prefecture, Japan
inferred← citeshttps://doi.org/10.12968/vetn.2023.14.1.24openalex-snapshot
Clinical features of hepatozoonosis in dogs and cats
inferred← citeshttps://doi.org/10.1371/journal.pntd.0012185openalex-snapshot
Molecular screening and genetic diversity of tick-borne pathogens associated with dogs and livestock ticks in Egypt
inferred← citeshttps://doi.org/10.1371/journal.pntd.0013806openalex-snapshot
The diversity of sandflies (Psychodidae: Phlebotominae) and the presence of Leishmania spp. DNA in potential vectors of the Mbaracayú Forest Biosphere Reserve, Canindeyú, Paraguay: New records and findings
inferred← citeshttps://doi.org/10.14196/sjva.v3i9.1731openalex-snapshot
Canine hepatozoonosis in a 4 month old intact male german shepherd dog in Ibadan, South West Nigeria: A case report
inferred← citeshttps://doi.org/10.14393/ufu.te.2013.22openalex-snapshot
Prevalência e caracterização molecular da espécie de Hepatozoon e parâmetros hematológicos e bioquímicos de cães (Canis familiaris) naturalmente infectados procedentes da microrregião de Uberlândia MG
inferred← citeshttps://doi.org/10.14432/j.macvetrev.2015.06.046openalex-snapshot
A Report of a Hepatozoon Canis Infection in a Dog with Transmissible Venereal Tumour
inferred← citeshttps://doi.org/10.1515/ap-2015-0003openalex-snapshot
Molecular detection of Dirofilaria immitis, Hepatozoon canis, Babesia spp., Anaplasma platys and Ehrlichia canis in dogs on Costa Rica
inferred← citeshttps://doi.org/10.1515/ap-2016-0098openalex-snapshot
Critical analysis of vector-borne infections in dogs: Babesia vogeli, Babesia gibsoni, Ehrlichia canis and Hepatozoon canis in Punjab, India
inferred← citeshttps://doi.org/10.1515/ap-2018-0069openalex-snapshot
Screening of Cercopithifilaria bainae and Hepatozoon canis in ticks collected from dogs of Northeastern Brazil
inferred← citeshttps://doi.org/10.1590/1678-4162-8855openalex-snapshot
Molecular diagnosis of Hepatozoon canis in symptomatic dogs in the city of Goiania, Goiás, Brazil
inferred← citeshttps://doi.org/10.1590/s1984-29612011000300002openalex-snapshot
Brazilian canine hepatozoonosis
inferred← citeshttps://doi.org/10.1590/s1984-29612015011openalex-snapshot
Survey of Ehrlichia canis, Babesia spp. and Hepatozoon spp. in dogs from a semiarid region of Brazil
inferred← citeshttps://doi.org/10.1645/15-732.1openalex-snapshot
Molecular Survey ofHepatozoon canisin Red Foxes (Vulpes vulpes) from Romania
inferred← citeshttps://doi.org/10.1645/ge-2672.1openalex-snapshot
Novel Hepatozoon in Vertebrates From the Southern United States
inferred← citeshttps://doi.org/10.18805/ijar.b-5420openalex-snapshot
Prevalence, Molecular Identification and Phylogenic Analysis of Hepatozoon canis from Naturally Infected Dogs in Andhra Pradesh, South India
inferred← citeshttps://doi.org/10.20506/rst.39.3.3175openalex-snapshot
Integrated management of blood-feeding arthropods in veterinary teaching facilities - Part 1: overview of haematophagous arthropods of interest in North-western Europe
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4197979/v1openalex-snapshot
Molecular investigation of ticks and tick-borne protozoan parasites (Apicomplexa: Cytauxzoon and Hepatozoon spp.) from Eurasian lynx (Lynx lynx) in northwestern China: first identification of Cytauxzoon manul in this host species
inferred← citeshttps://doi.org/10.21608/ejvs.2022.146290.1355openalex-snapshot
Molecular Identification of Hepatozoon canis in Ticks from Dogs in Siirt, Turkey
inferred← citeshttps://doi.org/10.24215/15142590e002openalex-snapshot
Evaluación de la eficacia de algunos fármacos para el tratamiento de la hepatozoonosis canina
inferred← citeshttps://doi.org/10.2460/javma.243.12.1705openalex-snapshot
Pathology in Practice
inferred← citeshttps://doi.org/10.2460/javma.248.6.621openalex-snapshot
Pathology in Practice
inferred← citeshttps://doi.org/10.2478/s11686-020-00221-2openalex-snapshot
The Discovery of Zoonotic Protozoans in Fleas Parasitizing on Pets as a Potential Infection Threat
inferred← citeshttps://doi.org/10.24998/maeusabed.1474199openalex-snapshot
Case Report of a Dog Heavily Infected With Hepatozoonosis
inferred← citeshttps://doi.org/10.26512/2015.06.d.18854openalex-snapshot
Estudo da ocorrência da infecção por Hepatozoon sp. em gatos domésticos de Brasília e regiões periurbanas
inferred← citeshttps://doi.org/10.2754/avb202291030277openalex-snapshot
A Molecular survey of Hepatozoon canis in dogs in the Siirt province of Turkey
inferred← citeshttps://doi.org/10.29005/ijcp.2022.14.1.56-58openalex-snapshot
MOLECULAR DIAGNOSIS AND THERAPEUTIC MANAGEMENT OF HEPATOZOON CANIS INFECTION IN DOGS
inferred← citeshttps://doi.org/10.2903/sp.efsa.2017.en-1171openalex-snapshot
Data collection for risk assessments on animal health (Acronym: DACRAH) : Final Report
inferred← citeshttps://doi.org/10.31248/jasvm2018.106openalex-snapshot
A review of some tick-borne pathogens of dogs
inferred← citeshttps://doi.org/10.3347/kjp.2017.55.5.561openalex-snapshot
First Case of Canine Infection with Hepatozoon canis (Apicomplexa: Haemogregarinidae) in the Republic of Korea
inferred← citeshttps://doi.org/10.3389/fvets.2022.964177openalex-snapshot
Concomitant Infections With Canine Parvovirus Type 2 and Intracellular Tick-Borne Pathogens in Two Puppy Dogs
inferred← citeshttps://doi.org/10.3390/ani12233335openalex-snapshot
High Prevalence and Genetic Variability of Hepatozoon canis in Grey Wolf (Canis lupus L. 1758) Population in Serbia
inferred← citeshttps://doi.org/10.3390/ani13111867openalex-snapshot
Molecular Survey and Genetic Characteristics of Vector-Borne Pathogens in Domestic Dogs from Four Regions of China
inferred← citeshttps://doi.org/10.3390/biology13060411openalex-snapshot
Molecular Detection and Genetic Variability of Hepatozoon canis in Golden Jackals (Canis aureus L. 1758) in Serbia
inferred← citeshttps://doi.org/10.3390/microorganisms11102374openalex-snapshot
Reevaluation of Hemoparasites in the Black Spiny-Tailed Iguana (Ctenosaura similis) with the First Pathological and Molecular Characterizations of Lankesterella desseri n. sp. and Redescription of Hepatozoon gamezi
inferred← citeshttps://doi.org/10.3390/pathogens10020231openalex-snapshot
Primary Tick-Borne Protozoan and Rickettsial Infections of Animals in Turkey
inferred← citeshttps://doi.org/10.3390/pathogens10101273openalex-snapshot
Ticks and Tick-Borne Diseases in Central America and the Caribbean: A One Health Perspective
inferred← citeshttps://doi.org/10.3390/pathogens10101339openalex-snapshot
Occurrence of Babesia Species and Co-Infection with Hepatozoon canis in Symptomatic Dogs and in Their Ticks in Eastern Romania
inferred← citeshttps://doi.org/10.3390/pathogens11010011openalex-snapshot
A Unique Case of Fatal Coinfection Caused by Leptospira spp. and Hepatozoon canis in a Red Fox Cub (Vulpes vulpes)
inferred← citeshttps://doi.org/10.3390/pathogens11030298openalex-snapshot
Potential Role of Birds in the Epidemiology of Coxiella burnetii, Coxiella-like Agents and Hepatozoon spp.
inferred← citeshttps://doi.org/10.3390/pathogens14080756openalex-snapshot
Morphometric and Molecular Insights into Hepatozoon spp. in Wild and Synanthropic Rodents from Southern and Southeastern Brazil
inferred← citeshttps://doi.org/10.3390/vetsci10110640openalex-snapshot
Molecular Survey of Hepatozoon canis Infection in Domestic Dogs from Sardinia, Italy
inferred← citeshttps://doi.org/10.34626/9fhj-db95openalex-snapshot
Fitness effects of Hepatozoon blood parasites in selected lizard species
inferred← citeshttps://doi.org/10.35537/10915/148720openalex-snapshot
Parasitología comparada. Modelos parasitarios
inferred← citeshttps://doi.org/10.35537/10915/67582openalex-snapshot
Aspectos diagnósticos y epidemiológicos de la piroplasmosis canina en áreas urbanas del sur del Gran Buenos Aires
inferred← citeshttps://doi.org/10.3906/vet-0801-11openalex-snapshot
Description of dogs naturally infected with Hepatozoon canis in the Aegean region of Turkey
inferred← citeshttps://doi.org/10.4102/jsava.v86i1.1307openalex-snapshot
Vector-borne diseases of small companion animals in Namibia: Literature review, knowledge gaps and opportunity for a One Health approach
inferred← citeshttps://doi.org/10.4102/jsava.v91i0.2023openalex-snapshot
Parasites of veterinary importance from domestic animals in uMkhanyakude district of KwaZulu-Natal province
inferred← citeshttps://doi.org/10.47027/duvetfd.1504235openalex-snapshot
Preliminary Study on the Genetic Diversity of Hepatozoon canis in Dogs and Rhipicephalus sanguineus sensu lato Ticks
inferred← citeshttps://doi.org/10.47262/bl/10.2.20240621openalex-snapshot
Prevalence and identification of zoonotic haemoparasites on bullfrogs (Hoplobatrachus tigerinus) as potential vectors for diseases in humans
inferred← citeshttps://doi.org/10.5433/1679-0359.2020v41n2p689openalex-snapshot
Molecular survey for the presence of tick-borne haemoparasites in dogs and ticks from the Atlantic Forest environment, Rio de Janeiro state, Brazil
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