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The Life Cycle of Contracaecum multipapillatum (von Drasche, 1882) Lucker, 1941 (Nematoda: Heterochelidae)
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inferred← citeshttps://doi.org/10.11646/zootaxa.5256.1.3zenodo-depositor-declared
The genus Contracaecum Raillet & Henry (Nematoda: Anisakidae): host and geographical distribution on Neotropical and Antarctic species
inferred← citeshttps://doi.org/10.1002/aff2.70100openalex-snapshot
Sinoatrial Contracaeciasis in Johnny Darters ( Etheostoma nigrum) and Plains Topminnow ( Fundulus sciadicus ) From the South Platte Drainage, Colorado
inferred← citeshttps://doi.org/10.1002/ece3.11122openalex-snapshot
Divvying up the pie: Tissue nutrient content is related to its parasite load
inferred← citeshttps://doi.org/10.1006/mpev.1998.0514openalex-snapshot
Ribosomal DNA and Phylogeny of the Ascaridoidea (Nemata: Secernentea): Implications for Morphological Evolution and Classification
inferred← citeshttps://doi.org/10.1007/bf00043006openalex-snapshot
The role of zooplankton in the transmission of helminth parasites to fish
inferred← citeshttps://doi.org/10.1007/bf00931790openalex-snapshot
The life cycle ofContracaecum osculatum (Rudolphi, 1802) sensu stricto (Nematoda, Ascaridoidea, Anisakidae) in view of experimental infections
inferred← citeshttps://doi.org/10.1007/s00436-002-0756-7openalex-snapshot
Growth of whaleworm (Anisakis simplex, Nematodes, Ascaridoidea, Anisakidae) third-stage larvae in paratenic fish hosts
inferred← citeshttps://doi.org/10.1007/s00436-008-1088-zopenalex-snapshot
Contracaecum pyripapillatum n. sp. (Nematoda: Anisakidae) and a description of C. multipapillatum (von Drasche, 1882) from the Australian pelican, Pelecanus conspicillatus
inferred← citeshttps://doi.org/10.1007/s00436-017-5528-5openalex-snapshot
Short communication: first report of nematodes parasitizing the four-eyed-fish, Anableps anableps (Pisces, Cyprinodontiformes)
inferred← citeshttps://doi.org/10.1007/s00436-017-5583-yopenalex-snapshot
A scanning electron microscopy study of early development in vitro of Contracaecum multipapillatum s.l. (Nematoda: Anisakidae) from a brown pelican (Pelecanus occidentalis) from the Gulf of California, Mexico
inferred← citeshttps://doi.org/10.1007/s00436-025-08533-wopenalex-snapshot
Detection of zoonotic nematodes in brown trout, Salmo trutta, an introduced popular edible freshwater fish in Australia
inferred← citeshttps://doi.org/10.1007/s12639-025-01842-yopenalex-snapshot
Report on nematode parasites in spot-billed pelicans (Pelecanus philippensis) and painted storks (Mycteria leucocephala) from Telineelapuram, Srikakulam District, AP, India
inferred← citeshttps://doi.org/10.1016/bs.apar.2020.01.037openalex-snapshot
History of Toxocara and the associated larva migrans
inferred← citeshttps://doi.org/10.1016/j.ijpara.2020.02.001openalex-snapshot
Odds ratios and hurdle models: a long-term analysis of parasite infection patterns in endangered young-of-the-year suckers from Upper Klamath Lake, Oregon, USA
inferred← citeshttps://doi.org/10.1016/j.ijppaw.2014.04.001openalex-snapshot
Recent advances in our knowledge of Australian anisakid nematodes
inferred← citeshttps://doi.org/10.1016/j.mcp.2010.09.003openalex-snapshot
Mutation scanning-coupled sequencing of nuclear ribosomal DNA spacers as a tool for the specific identification of different Contracaecum (Nematoda: Anisakidae) larval types
inferred← citeshttps://doi.org/10.1016/j.parint.2022.102664openalex-snapshot
Occurrence and molecular identification of nematodes from blue mackerel Scomber australasicus Cuvier in Australian waters
inferred← citeshttps://doi.org/10.1016/j.vetpar.2004.09.026openalex-snapshot
Larval Contracaecum sp. (Nematoda: Anisakidae) in Hoplias malabaricus and Hoplerythrinus unitaeniatus (Osteichthyes: Erythrinidae) of economic importance in occidental marshlands of Maranhão, Brazil
inferred← citeshttps://doi.org/10.1016/j.vetpar.2009.08.002openalex-snapshot
Larval Contracaecum sp. (Nematoda: Anisakidae) in the Great Cormorant [Phalacrocorax carbo (L., 1758)] from north-eastern Poland: A morphological and morphometric analysis
inferred← citeshttps://doi.org/10.1016/j.vetpar.2023.110050openalex-snapshot
Fecundity, in vitro early larval development and karyotype of the zoonotic nematode Anisakis pegreffii
inferred← citeshttps://doi.org/10.1016/s0065-308x(08)60573-4openalex-snapshot
Anisakis and Anisakiasis
inferred← citeshttps://doi.org/10.1017/s0022149x24000610openalex-snapshot
First report of a morulated Ascaridoidea (Nematoda) egg in an avian coprolite from the Paleogene of the Paraíba Valley, State of São Paulo, Brazil
inferred← citeshttps://doi.org/10.1017/s0031182000067329openalex-snapshot
Hatching, survival, activity and penetration efficiency of second-stage larvae of Anguillicola crassus (Nematoda)
inferred← citeshttps://doi.org/10.1017/s0031182011000370openalex-snapshot
Intensity-dependent host mortality: what can it tell us about larval growth strategies in complex life cycle helminths?
inferred← citeshttps://doi.org/10.1111/are.15774openalex-snapshot
Molecular characterization of zoonotic anisakid Contracaecum spp. larvae in some fish species from Lake Nasser, Egypt
inferred← citeshttps://doi.org/10.1111/jai.13848openalex-snapshot
Detection of Contracaecum multipapillatum (Nematoda: Anisakidae) in the indigenous killifish Aphanius hormuzensis (Teleostei; Aphaniidae) and its histopathological effects: A review of Iranian Aphanius species parasites
inferred← citeshttps://doi.org/10.1111/jfd.13711openalex-snapshot
Contracaecum nematode parasites in hillstream loaches of the Western Ghats, India
inferred← citeshttps://doi.org/10.1139/z92-041openalex-snapshot
Effect of temperature on egg hatching and survival of larvae of Anisakis simplex B (Nematoda: Ascaridoidea)
inferred← citeshttps://doi.org/10.1139/z93-178openalex-snapshot
Aspects of the life cycle and morphology of Hysterothylacium aduncum (Rudolphi, 1802) (Nematoda, Ascaridoidea, Anisakidae)
inferred← citeshttps://doi.org/10.1645/0022-3395(2000)086[0380:potana]2.0.co;2openalex-snapshot
PHYLOGENY OF THE ASCARIDOIDEA (NEMATODA: ASCARIDIDA) BASED ON THREE GENES AND MORPHOLOGY: HYPOTHESES OF STRUCTURAL AND SEQUENCE EVOLUTION
inferred← citeshttps://doi.org/10.1645/18-69openalex-snapshot
Variation in Helminth Parasite Component Communities of Gambusia affinis
inferred← citeshttps://doi.org/10.1654/4337.1openalex-snapshot
Taxonomy and Faunistics of the Helminth Parasites of Clarias gariepinus (Burchell, 1822), and Oreochromis mossambicus (Peters, 1852) from Temporary Pans and Pools in the Save-Runde River Floodplain, Zimbabwe
inferred← citeshttps://doi.org/10.1654/4492.1openalex-snapshot
Helminths of Belted Kingfishers, Megaceryle alcyon Linnaeus, 1758, from a Fish Hatchery in Ohio, U.S.A
inferred← citeshttps://doi.org/10.18785/gcr.1701.04openalex-snapshot
Parasites of the American White Pelican
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3395571/v1openalex-snapshot
Helminthic parasites of invasive alien fish hosts in Marikina River system, Philippines: Revealing new parasite hosts and species records
inferred← citeshttps://doi.org/10.2478/s11687-011-0007-5openalex-snapshot
Helminth infection in Mugil incilis from Cartagena de Indias, Colombian Caribbean coast
inferred← citeshttps://doi.org/10.3354/dao03147openalex-snapshot
Early development and life cycle of Contracaecum multipapillatum s.l. from a brown pelican Pelecanus occidentalis in the Gulf of California, Mexico
inferred← citeshttps://doi.org/10.3354/dao03168openalex-snapshot
Hematology and condition factor of tui chub and fathead minnow parasitized by nematode from Upper Klamath Lake, Oregon, USA
inferred← citeshttps://doi.org/10.3390/ani13243793openalex-snapshot
The Occurrence of Freshwater Fish-Borne Zoonotic Helminths in Italy and Neighbouring Countries: A Systematic Review
inferred← citeshttps://doi.org/10.3390/pathogens11111315openalex-snapshot
Unusual Localization of Hysterothylacium Incurvum in Xiphias gladius (Linnaeus 1758) Caught in the Atlantic Ocean
inferred← citeshttps://doi.org/10.4102/ojvr.v86i1.1659openalex-snapshot
Seasonal occurrence of metazoan parasites in Tigerfish, Hydrocynus vittatus Castelnau, 1861 (Characiformes: Alestidae) from Sanyati Basin, Lake Kariba, Zimbabwe
inferred← citeshttps://doi.org/10.7717/peerj.1722openalex-snapshot
Occurrence ofTerranovalarval types (Nematoda: Anisakidae) in Australian marine fish with comments on their specific identities
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