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Species of Angiostrongylus (Nematoda: Metastrongyloidea) in wildlife: A review

https://doi.org/10.1016/j.ijppaw.2015.02.006

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What this work says

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

inferredcites →https://doi.org/10.1186/1756-3305-5-70zenodo-depositor-declared

Twenty two cases of canine neural angiostrongylosis in eastern Australia (2002-2005) and a review of the literature

inferredcites →https://doi.org/10.1001/archneur.1971.00480340114020openalex-snapshot

Angiostrongylosis: In the Pacific and Southeast Asia.

inferredcites →https://doi.org/10.1007/978-3-319-30009-2_1004openalex-snapshot

Angiostrongylus Cantonensis Infections

inferredcites →https://doi.org/10.1007/bf00931834openalex-snapshot

The common frog (Rana temporaria) as a potential paratenic and intermediate host forAngiostrongylus vasorum

inferredcites →https://doi.org/10.1007/s00436-003-1000-9openalex-snapshot

Angiostrongylus vasorum (Baillet, 1866) Kamensky, 1905: emergence of third-stage larvae from infected Biomphalaria glabrata snails

inferredcites →https://doi.org/10.1007/s004360000316openalex-snapshot

Helminth parasites of the eurasian badger ( Meles meles L.) in Spain: a biogeographic approach

inferredcites →https://doi.org/10.1016/0020-7519(74)90020-4openalex-snapshot

Experimental hybridization of Angiostrongylus mackerrasae, Bhaibulaya, 1968 and Angiostrongylus cantonensis (Chen, 1935)

inferredcites →https://doi.org/10.1016/0020-7519(75)90091-0openalex-snapshot

Comparative studies on the life history of Angiostrongylus mackerrasae Bhaibulaya, 1968 and Angiostrongylus cantonensis (Chen, 1935)

inferredcites →https://doi.org/10.1016/0169-4758(85)90177-2openalex-snapshot

Abdominal angiostrongyliasis: A problem of public health

inferredcites →https://doi.org/10.1016/0169-4758(93)90182-fopenalex-snapshot

Nematode parasites of vertebrates. Their development and transmission

inferredcites →https://doi.org/10.1016/j.ijpara.2005.01.014openalex-snapshot

Australian ecosystems, capricious food chains and parasitic consequences for people

inferredcites →https://doi.org/10.1016/j.ijppaw.2013.10.003openalex-snapshot

Angiostrongylus vasorum in wolves in Italy

inferredcites →https://doi.org/10.1016/j.meegid.2010.01.013openalex-snapshot

Elucidating the spread of the emerging canid nematode Angiostrongylus vasorum between Palaearctic and Nearctic ecozones

inferredcites →https://doi.org/10.1016/j.pt.2004.11.006openalex-snapshot

Angiostrongylus vasorum: a real heartbreaker

inferredcites →https://doi.org/10.1016/j.vetpar.2008.02.030openalex-snapshot

Angiostrongylus vasorum and Eucoleus aerophilus in foxes (Vulpes vulpes) in Great Britain

inferredcites →https://doi.org/10.1016/j.vetpar.2010.07.015openalex-snapshot

Angiostrongylus species in wild carnivores in the Iberian Peninsula

inferredcites →https://doi.org/10.1016/j.vetpar.2012.11.009openalex-snapshot

Tawny frogmouths and brushtail possums as sentinels for Angiostrongylus cantonensis, the rat lungworm

inferredcites →https://doi.org/10.1016/s0020-7519(00)00133-8openalex-snapshot

Neuro-angiostrongyliasis: unresolved issues

inferredcites →https://doi.org/10.1016/s0031-3025(16)39339-4openalex-snapshot

Human larval meningitis possibly following lettuce ingestion in Brisbane

inferredcites →https://doi.org/10.1016/s1473-3099(08)70229-9openalex-snapshot

Human angiostrongyliasis

inferredcites →https://doi.org/10.1017/s0022149x00013547openalex-snapshot

Occurrence of Angiostrongylus vasorum in the lungs of the Brazilian fox Dusicyon vetulus

inferredcites →https://doi.org/10.1017/s0022149x10000398openalex-snapshot

Variation in the helminth community structure of three sympatric sigmodontine rodents from the coastal Atlantic Forest of Rio de Janeiro, Brazil

inferredcites →https://doi.org/10.1017/s0031182000011707openalex-snapshot

On a Collection of Nematodes from Nigerian Mammals (chiefly Rodents)

inferredcites →https://doi.org/10.1017/s0031182000069572openalex-snapshot

A new species of Angiostrongylus in an Australian rat, Rattus fuscipes

inferredcites →https://doi.org/10.1017/s0031182008005258openalex-snapshot

Angiostrongylus vasorumfrom South America and Europe represent distinct lineages

inferredcites →https://doi.org/10.1046/j.1365-3156.2003.01035.xopenalex-snapshot

Présence d'Angiostrongylus cantonensis en Haïti

inferredcites →https://doi.org/10.1051/parasite/1935134312openalex-snapshot

Un nouveau nématode pulmonaire, Pulmonema cantonensis, n. g., n. sp.

inferredcites →https://doi.org/10.1051/parasite/1970455597openalex-snapshot

Révision de la systématique du genre Angiostrongylus Kamensky 1905 (Nematoda : Metastrongyloidea)

inferredcites →https://doi.org/10.1051/parasite/1972471131openalex-snapshot

Description d’une nouvelle espèce d’Aelurostrongylus parasite de Rongeur africain

inferredcites →https://doi.org/10.1051/parasite/1973484567openalex-snapshot

Angiostrongylus vasorum (Baillet, 1866). Etude biologique et morphologique

inferredcites →https://doi.org/10.1051/parasite/1974491069openalex-snapshot

Le cycle évolutif de Morerastrongylus andersoni (Petter, 1972)

inferredcites →https://doi.org/10.1051/parasite/1975504469openalex-snapshot

Mode de pénétration et localisation des larves de Morerastrongylus andersoni (Petter, 1972) (Metastrongyloidea, Nematoda) chez l’hôte intermédiaire

inferredcites →https://doi.org/10.1071/ma05063openalex-snapshot

Neuroangiostrongyliasis: disease in wildlife and humans

inferredcites →https://doi.org/10.1071/zo04007openalex-snapshot

The helminth parasites of Melomys cervinipes (Rodentia : Muridae : Hydromyinae)

inferredcites →https://doi.org/10.1071/zo06061openalex-snapshot

Occurrence of Angiostrongylus species (Nematoda) in populations of Rattus rattus and Rattus fuscipes in coastal forests of south-eastern Australia

inferredcites →https://doi.org/10.1071/zo9550001openalex-snapshot

The life history of the rat lung-worm, Angiostrongylus cantonensis (Chen) (Nematoda: Metastrongylidae).

inferredcites →https://doi.org/10.1079/9780851994215.0000openalex-snapshot

Nematode parasites of vertebrates: their development and transmission

inferredcites →https://doi.org/10.1079/joh200152openalex-snapshot

Helminths in the wolf, Canis lupus, from north-western Spain

inferredcites →https://doi.org/10.1080/00034983.1968.11686591openalex-snapshot

Early migration and pathogenicity ofAngiostrongylus cantonensisin laboratory rats

inferredcites →https://doi.org/10.1093/cid/cit444openalex-snapshot

Severe Hemorrhagic Meningoencephalitis Due to Angiostrongylus cantonensis Among Young Children in Sydney, Australia

inferredcites →https://doi.org/10.1093/oxfordjournals.aje.a120946openalex-snapshot

STUDIES ON EOSINOPHILIC MENINGITIS

inferredcites →https://doi.org/10.1111/avj.12082openalex-snapshot

Patent A ngiostrongylus mackerrasae infection in a black flying fox ( P teropus alecto)

inferredcites →https://doi.org/10.1111/avj.12116openalex-snapshot

Neuroangiostrongyliasis due to A ngiostrongylus cantonensis in gang‐gang cockatoos ( C allocephalon fimbriatum)

inferredcites →https://doi.org/10.1111/j.1445-5994.1979.tb03402.xopenalex-snapshot

EOSINOPHILIC MENINGITIS

inferredcites →https://doi.org/10.1111/j.1445-5994.1980.tb03725.xopenalex-snapshot

BRIEF COMMUNICATION: ANGIOSTRONGYLIASS IN AUSTRALIA

inferredcites →https://doi.org/10.1111/j.1751-0813.1976.tb00124.xopenalex-snapshot

GRANULOMATOUS ENCEPHALOMYELITIS OF PUPPIES DUE TO

inferredcites →https://doi.org/10.1111/j.1751-0813.1978.tb00354.xopenalex-snapshot

ANGIOSTRONGYLUS CANTONENSIS INFECTION OF THE BRAIN OF A CAPTIVE BENNETT'S WALLABY (MACROPUS RUFOGRISEUS)

inferredcites →https://doi.org/10.1111/j.1751-0813.1987.tb15181.xopenalex-snapshot

Canine neural angiostrongylosis: the clinical and therapeutic features of 55 natural cases

inferredcites →https://doi.org/10.1111/j.1751-0813.1991.tb03131.xopenalex-snapshot

Equine neural angiostrongylosis

inferredcites →https://doi.org/10.1111/j.1751-0813.1992.tb07505.xopenalex-snapshot

Angiostrongylosis in dogs in Sydney

inferredcites →https://doi.org/10.1111/j.1751-0813.1997.tb14194.xopenalex-snapshot

Neural angiostrongylosis in three captive rufous bettongs (Aepyprymnus rufescens)

inferredcites →https://doi.org/10.1111/j.1751-0813.1998.tb10121.xopenalex-snapshot

Cerebrospinal angiostrongyliasis in five captive tamarins (Sanguinus spp)

inferredcites →https://doi.org/10.1111/j.1751-0813.1999.tb12095.xopenalex-snapshot

Angiostrongylus cantonensis infection in grey‐headed fruit bats (Pteropus poliocephalus)

inferredcites →https://doi.org/10.1111/j.1751-0813.2002.tb11039.xopenalex-snapshot

Neuro‐angiostrongylosis in wild Black and Grey‐headed flying foxes (Pteropus spp)

inferredcites →https://doi.org/10.1111/j.1751-0813.2010.00660.xopenalex-snapshot

Neuroangiostrongyliasis and other parasites in tawny frogmouths (Podargus strigoides) in south‐eastern Queensland

inferredcites →https://doi.org/10.1111/j.2042-3292.2000.tb01754.xopenalex-snapshot

Verminous meningoencephalomyelitis by Angiostrongylus (=Parastrongylus) cantonensis in an American Miniature Horse

inferredcites →https://doi.org/10.1126/science.158.3804.1057openalex-snapshot

Angiostrongylus cantonensis : Proof of Direct Transmission with Its Epidemiological Implications

inferredcites →https://doi.org/10.1136/vr.135.19.447openalex-snapshot

Canine angiostrongylosis: a review

inferredcites →https://doi.org/10.1139/z03-211openalex-snapshot

Angiostrongylus vasorumandCrenosoma vulpisin red foxes (Vulpes vulpes) in Newfoundland, Canada

inferredcites →https://doi.org/10.11646/zootaxa.1721.1.1openalex-snapshot

Checklist of helminth parasites in wild carnivore mammals from Brazil

inferredcites →https://doi.org/10.1186/1756-3305-7-396openalex-snapshot

Moving the boundaries to the South-East: first record of autochthonous Angiostrongylus vasorum infection in a dog in Vojvodina province, northern Serbia

inferredcites →https://doi.org/10.14943/jjvr.27.1-2.5openalex-snapshot

Studies on the parasite fauna of Thailand. I Two new metastrongylid nematodes, Angiostrongylus siamensis sp. n. and Thaistrongylus harinasutai gen. et sp. n. (Metastrongyloidea; Angiostrongylidae) from wild rats.

inferredcites →https://doi.org/10.14943/jjvr.28.4.114openalex-snapshot

Report on the prevalence and experimental infections of Angiostrongylus siamensis Ohbayashi, Kamiya et Bhaibulaya, 1979, parasitic in the mesenteric arteries of rodents in Thailand.

inferredcites →https://doi.org/10.14943/jjvr.31.1.49openalex-snapshot

Incidence of Angiostrongylus siamensis in small mammals at Nakorn Nayok, Thailand.

inferredcites →https://doi.org/10.14943/jjvr.31.2.71openalex-snapshot

A case of abdominal angiostrongyliasis in a monkey.

inferredcites →https://doi.org/10.14943/jjvr.31.3-4.151openalex-snapshot

Development and migration route of Angiostrongylus siamensis in mice.

inferredcites →https://doi.org/10.14943/jjvr.36.1.47openalex-snapshot

Angiostrongylus sandarsae Alicata, 1968 (Nematoda: Metastrongyloidea) from Praomys natalensis in Kenya.

inferredcites →https://doi.org/10.1590/s0034-89101997000300014openalex-snapshot

Registro de Achatina fulica Bowdich, 1822 (Mollusca, Gastropoda) no Brasil: caramujo hospedeiro intermediário da angiostrongilíase

inferredcites →https://doi.org/10.1590/s0036-46651990000300001openalex-snapshot

Identificação de roedores silvestres como hospedeiros do Angiostrongylus costaricensis no sul do Brasil

inferredcites →https://doi.org/10.1590/s0037-86821998000300006openalex-snapshot

Angiostrongylus costaricensis and the intermediate hosts: observations on elimination of L3 in the mucus and inoculation of L1 through the tegument of mollucs

inferredcites →https://doi.org/10.1590/s0074-02761993000300020openalex-snapshot

On the diversity of mollusc intermediate hosts of Angiostrongylus costaricensis Morera & Cespedes, 1971 in southern Brazil

inferredcites →https://doi.org/10.1590/s0074-02761995000600010openalex-snapshot

Angiostrongylus costaricensis life cycle: a new proposal

inferredcites →https://doi.org/10.1590/s0074-02761999000400022openalex-snapshot

Penetration Sites and Migratory Routes of Angiostrongylus costaricensis in the Experimental Intermediate Host (Sarasinula marginata)

inferredcites →https://doi.org/10.1590/s0074-02762005000400012openalex-snapshot

Angiostrongylus costaricensis: complete redescription of the migratory pathways based on experimental Sigmodon hispidus infection

inferredcites →https://doi.org/10.1638/05-075.1openalex-snapshot

PARASITES OF FREE-RANGING SMALL CANIDS AND FELIDS IN THE BOLIVIAN CHACO

inferredcites →https://doi.org/10.1645/0022-3395(2001)087[1174:agitif]2.0.co;2openalex-snapshot

Angiocaulus gubernaculatusin the Island Fox (Urocyon littoralis) From the California Channel Islands and Comments on the Diagnosis of Angiostrongylidae Nematodes in Canid and Mustelid Hosts

inferredcites →https://doi.org/10.1645/0022-3395(2002)088[1024:pacnei]2.0.co;2openalex-snapshot

Parastrongylus (=Angiostrongylus) cantonensis Now Endemic in Louisiana Wildlife

inferredcites →https://doi.org/10.1645/ge-1340.1openalex-snapshot

A New Angiostrongylid (Nematoda) Species from the Pulmonary Arteries of Akodon azarae (Rodentia: Cricetidae) in Argentina

inferredcites →https://doi.org/10.1645/ge-2013.1openalex-snapshot

A New Metastrongilid Species (Nematoda: Metastrongylidae): A Lungworm from Akodon montensis (Rodentia: Sigmodontinae) in Brazil

inferredcites →https://doi.org/10.1645/ge-3128.1openalex-snapshot

Histopathology Associated with Angiostrongylosis inAkodonSpecies (Rodentia: Sigmodontinae) from Sierra de la Ventana, Buenos Aires, Argentina

inferredcites →https://doi.org/10.1645/ge-3171.1openalex-snapshot

A New Metastrongyloidean Species (Nematoda) Parasitizing Pulmonary Arteries ofPuma(Herpailurus)yagouaroundi(É. Geoffroy, 1803) (Carnivora: Felidae) from Brazil

inferredcites →https://doi.org/10.1645/ge-653r.1openalex-snapshot

Endemic Infections of Parastrongylus (=Angiostrongylus) costaricensis in Two Species of Nonhuman Primates, Raccoons, and an Opossum From Miami, Florida

inferredcites →https://doi.org/10.1647/2004-024.1openalex-snapshot

Angiostrongylus cantonensis as a Cause of Cerebrospinal Disease in a Yellow-tailed Black Cockatoo (Calyptorhynchus funereus) and Two Tawny Frogmouths (Podargus strigoides)

inferredcites →https://doi.org/10.2307/3276595openalex-snapshot

Studies on Angiostrongylus cantonensis in Molluscan Intermediate Hosts

inferredcites →https://doi.org/10.2307/3277116openalex-snapshot

Angiostrongylus sandarsae sp. n. (Nematoda: Metastrongyloidea), a Lungworm of Rodents in Mozambique, East Africa

inferredcites →https://doi.org/10.2307/3277901openalex-snapshot

Angiostrongylus schmidti sp. n. (Nematoda: Metastrongyloidea) from the Rice Rat, Oryzomys palustris, in Florida, with a Key to the Species of Angiostrongylus Kamensky, 1905

inferredcites →https://doi.org/10.2307/3278969openalex-snapshot

CIH Keys to the Nematode Parasites of Vertebrates

inferredcites →https://doi.org/10.2307/3279604openalex-snapshot

A New Definitive Natural Host of Angiostrongylus costaricensis (Morera and Cespedes 1971)

inferredcites →https://doi.org/10.2307/3280170openalex-snapshot

First Report of Angiostrongylus costaricensis Morera and Céspedes 1971 in the United States

inferredcites →https://doi.org/10.2307/3281599openalex-snapshot

Systematics of Species Referred to the Genus angiostrongylus

inferredcites →https://doi.org/10.2460/ajvr.1970.31.01.131openalex-snapshot

Life History of the Canine Lungworm Angiostrongylus vasorum (Baillet)

inferredcites →https://doi.org/10.3201/eid0803.010316openalex-snapshot

Enzootic Angiostrongyluscantonensis in Rats and Snails after an Outbreak of Human Eosinophilic Meningitis, Jamaica

inferredcites →https://doi.org/10.3760/cma.j.issn.1673-4904.2002.06.003openalex-snapshot

Parasitic meningitis

inferredcites →https://doi.org/10.4267/2042/67410openalex-snapshot

Recherches sur le cycle évolutif du Strongle des vaisseaux du Chien

inferredcites →https://doi.org/10.4269/ajtmh.1973.22.348openalex-snapshot

ANGIOSTRONGYLUS COSTARICENSIS IN PANAMA

inferredcites →https://doi.org/10.4269/ajtmh.1973.22.613openalex-snapshot

LIFE HISTORY AND REDESCRIPTION OF ANGIOSTRONGYLUS COSTARICENSIS MORERA AND CÉSPEDES, 1971

inferredcites →https://doi.org/10.4269/ajtmh.1981.30.963openalex-snapshot

First Record of Angiostrongylus cantonensis in Cuba

inferredcites →https://doi.org/10.4269/ajtmh.1983.32.1460openalex-snapshot

First Record of Angiostrongylus Costaricensis Morera and Céspedes, 1971 in Ecuador

inferredcites →https://doi.org/10.4269/ajtmh.1986.35.319openalex-snapshot

First Report of Angiostrongylus Cantonensis in Puerto Rico

inferredcites →https://doi.org/10.4269/ajtmh.1988.38.568openalex-snapshot

The Finding of Angiostrongylus Cantonensis in Rats in New Orleans

inferredcites →https://doi.org/10.4269/ajtmh.1990.42.70openalex-snapshot

Eosinophilic Meningoencephalitis Due to Angiostrongylus Cantonensis as the Cause of Death in Captive Non-Human Primates

inferredcites →https://doi.org/10.5694/j.1326-5377.1975.tb111586.xopenalex-snapshot

EOSINOPHILIC MENINGITIS (ANGIOSTRONGYLOSIS): A PROBABLE CASE

inferredcites →https://doi.org/10.5694/j.1326-5377.1987.tb133461.xopenalex-snapshot

Eosinophilic meningoencephalitis with permanent sequelae

inferredcites →https://doi.org/10.5694/j.1326-5377.1999.tb127872.xopenalex-snapshot

Parasitic meningitis

inferredcites →https://doi.org/10.5694/j.1326-5377.1999.tb127880.xopenalex-snapshot

A fatal case of angiostrongyliasis in an 11‐month‐old infant

inferredcites →https://doi.org/10.5694/j.1326-5377.2003.tb05623.xopenalex-snapshot

First report of human angiostrongyliasis acquired in Sydney

inferredcites →https://doi.org/10.5694/mja12.11085openalex-snapshot

Angiostrongylus meningoencephalitis: survival from minimally conscious state to rehabilitation

inferredcites →https://doi.org/10.7589/0090-3558-41.4.816openalex-snapshot

Angiostrongylus vasorum Infection in a Coyote (Canis latrans) from Newfoundland and Labrador, Canada

inferredcites →https://doi.org/10.7589/2013-03-050openalex-snapshot

Angiostrongylus cantonensis (Nematoda: Metastrongylidae) in the Ryukyu Islands Tree Rat (Diplothrix legata)

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

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inferred← citeshttps://doi.org/10.1016/j.crpvbd.2021.100033openalex-snapshot

Using cerebrospinal fluid to confirm Angiostrongylus cantonensis as the cause of canine neuroangiostrongyliasis in Australia where A. cantonensis and Angiostrongylus mackerrasae co-exist

inferred← citeshttps://doi.org/10.1016/j.crpvbd.2024.100179openalex-snapshot

Older urban rats are infected with the zoonotic nematode Angiostrongylus cantonensis

inferred← citeshttps://doi.org/10.1016/j.dci.2019.103579openalex-snapshot

Physiology and immunity of the invasive giant African snail, Achatina (Lissachatina) fulica, intermediate host of Angiostrongylus cantonensis

inferred← citeshttps://doi.org/10.1016/j.fawpar.2021.e00119openalex-snapshot

Newly developed SYBR Green-based quantitative real-time PCRs revealed coinfection evidence of Angiostrongylus cantonensis and A. malaysiensis in Achatina fulica existing in Bangkok Metropolitan, Thailand

inferred← citeshttps://doi.org/10.1016/j.fawpar.2021.e00128openalex-snapshot

Co-occurrence of Angiostrongylus malaysiensis and Angiostrongylus cantonensis DNA in cerebrospinal fluid: Evidence from human eosinophilic meningitis after ingestion of raw snail dish in Thailand

inferred← citeshttps://doi.org/10.1016/j.ijppaw.2017.05.004openalex-snapshot

Eosinophilic meningoencephalitis associated with rat lungworm (Angiostrongylus cantonensis) migration in two nine-banded armadillos (Dasypus novemcinctus) and an opossum (Didelphis virginiana) in the southeastern United States

inferred← citeshttps://doi.org/10.1016/j.ijppaw.2018.12.011openalex-snapshot

Zoonotic nematodes of wild carnivores

inferred← citeshttps://doi.org/10.1016/j.ijppaw.2021.05.003openalex-snapshot

Angiostrongylus vasorum in foxes (Vulpes vulpes) and wolves (Canis lupus italicus) from Abruzzo region, Italy

inferred← citeshttps://doi.org/10.1016/j.ijppaw.2025.101046openalex-snapshot

First record of Angiostrongylus cantonensis infection in Diplothrix legata (Rodentia: Muridae) in Tokunoshima Island, Japan

inferred← citeshttps://doi.org/10.1016/j.ijppaw.2026.101256openalex-snapshot

Cotton-top tamarins (Saguinus oedipus) can serve as definitive hosts of the rodent metastrongyloid parasite Angiostrongylus dujardini and develop fatal infections

inferred← citeshttps://doi.org/10.1016/j.onehlt.2022.100426openalex-snapshot

Paratenic hosts of Angiostrongylus cantonensis and their relation to human neuroangiostrongyliasis globally

inferred← citeshttps://doi.org/10.1016/j.onehlt.2023.100628openalex-snapshot

Fatal neural angiostrongyliasis in the Bolivian squirrel monkey (Saimiri boliviensis boliviensis) leading to defining Angiostrongylus cantonensis risk map at a zoo in Australia

inferred← citeshttps://doi.org/10.1016/j.onehlt.2023.100658openalex-snapshot

Stressed snails release Angiostrongylus cantonensis (rat lungworm) larvae in their slime

inferred← citeshttps://doi.org/10.1016/j.parint.2016.04.005openalex-snapshot

Fatal Angiostrongylus dujardini infection in callitrichid monkeys and suricates in an Italian zoological garden

inferred← citeshttps://doi.org/10.1016/j.parint.2018.09.006openalex-snapshot

Molecular phylogeography and genetic diversity of Angiostrongylus cantonensis and A. malaysiensis (Nematoda: Angiostrongylidae) based on 66-kDa protein gene

inferred← citeshttps://doi.org/10.1016/j.parint.2020.102058openalex-snapshot

Alien parasitic infections in the endangered Ryukyu long-furred rat (Diplothrix legata) on Amami-Oshima Island, Japan

inferred← citeshttps://doi.org/10.1016/j.parint.2023.102829openalex-snapshot

Angiostrongylus dujardini infection in a coconut lorikeet (Trichoglossus haematodus) from a zoological garden in Switzerland

inferred← citeshttps://doi.org/10.1016/j.pt.2015.07.001openalex-snapshot

Felid Lungworms and Heartworms in Italy: More Questions than Answers?

inferred← citeshttps://doi.org/10.1016/j.rvsc.2019.08.008openalex-snapshot

Cardiopulmonary nematode infections in wild canids: Does the key lie on host-prey-parasite evolution?

inferred← citeshttps://doi.org/10.1016/j.rvsc.2020.10.023openalex-snapshot

Angiostrongylus spp. (Nematoda; Metastrongyloidea) of global public health importance

inferred← citeshttps://doi.org/10.1016/j.vetpar.2015.08.016openalex-snapshot

First report of a naturally patent infection of Angiostrongylus costaricensis in a dog

inferred← citeshttps://doi.org/10.1016/j.vetpar.2016.08.017openalex-snapshot

The white-nosed coati (Nasua narica) is a naturally susceptible definitive host for the zoonotic nematode Angiostrongylus costaricensis in Costa Rica

inferred← citeshttps://doi.org/10.1016/j.vetpar.2016.09.007openalex-snapshot

Angiostrongylus chabaudi in felids: New findings and a review of the literature

inferred← citeshttps://doi.org/10.1016/j.vetpar.2016.12.006openalex-snapshot

Use of a commercial serologic test for Angiostrongylus vasorum for the detection of A. chabaudi in wildcats and A. daskalovi in badgers

inferred← citeshttps://doi.org/10.1016/j.vetpar.2018.03.011openalex-snapshot

Prevalence of Angiostrongylus vasorum, Aelurostrongylus abstrusus and Crenosoma vulpis larvae in native slug populations in Germany

inferred← citeshttps://doi.org/10.1016/j.vprsr.2019.100363openalex-snapshot

Angiostrongylus cantonensis central nervous system infection in captive callitrichids in Texas

inferred← citeshttps://doi.org/10.1017/s0022149x17000244openalex-snapshot

Cytochrome c oxidase subunit I haplotype reveals high genetic diversity of Angiostrongylus malaysiensis (Nematoda: Angiostrongylidae)

inferred← citeshttps://doi.org/10.1017/s0022149x1700061xopenalex-snapshot

Angiostrongylus mackerrasae and A. cantonensis (Nematoda: Metastrongyloidea) belong to same genetic lineage: evidence from mitochondrial protein-coding genes

inferred← citeshttps://doi.org/10.1017/s0022149x18000779openalex-snapshot

The first report of cerebral, pulmonary and gastrointestinal angiostrongyliasis in the water rat Hydromys chrysogaster from Queensland, Australia

inferred← citeshttps://doi.org/10.1017/s0022149x18000822openalex-snapshot

Invasive slug Meghimatium pictum (Stoliczka, 1873) infected by Angiostrongylus costaricensis Morera & Céspedes, 1971, and the possible risk of human infection associated with grape consumption

inferred← citeshttps://doi.org/10.1017/s0022149x19000270openalex-snapshot

Annotated catalogue of species of Angiostrongylus and the related genera Gallegostrongylus, Rodentocaulus and Stefanskostrongylus (Nematoda: Metastrongyloidea, Angiostrongylidae)

inferred← citeshttps://doi.org/10.1017/s0022149x21000341openalex-snapshot

Leukogram and cortisol parameters in Swiss mice experimentally infected withAngiostrongylus costaricensis

inferred← citeshttps://doi.org/10.1017/s0022149x21000602openalex-snapshot

Molossinema wimsatti infection in the brain of Pallas's mastiff bats (Molossus molossus)

inferred← citeshttps://doi.org/10.1017/s0022149x22000761openalex-snapshot

The invasive giant African land snail,Achatina fulica(Gastropoda: Pulmonata): global geographical distribution of this species as host of nematodes of medical and veterinary importance

inferred← citeshttps://doi.org/10.1017/s0031182016000640openalex-snapshot

An epidemiological study ofA. cantonensisin Jamaica subsequent to an outbreak of human cases of eosinophilic meningitis in 2000

inferred← citeshttps://doi.org/10.1017/s0031182016000652openalex-snapshot

Angiostrongylus cantonensis: a review of its distribution, molecular biology and clinical significance as a human pathogen

inferred← citeshttps://doi.org/10.1017/s003118201600069xopenalex-snapshot

Comparative pathogenesis of eosinophilic meningitis caused by Angiostrongylus mackerrasae and Angiostrongylus cantonensis in murine and guinea pig models of human infection

inferred← citeshttps://doi.org/10.1017/s0031182017001433openalex-snapshot

Larval development ofAngiostrongylus chabaudi, the causative agent of feline angiostrongylosis, in the snailCornu aspersum

inferred← citeshttps://doi.org/10.1017/s0031182020000232openalex-snapshot

The mitochondrial genome of Angiostrongylus mackerrasae is distinct from A. cantonensis and A. malaysiensis

inferred← citeshttps://doi.org/10.1017/s003118202000164xopenalex-snapshot

Variation in Angiostrongylus cantonensis infection in definitive and intermediate hosts in Hawaii, a global hotspot of rat lungworm disease

inferred← citeshttps://doi.org/10.1017/s0031182022000191openalex-snapshot

A validated high-throughput method for assaying rat lungworm (Angiostrongylus cantonensis) motility when challenged with potentially anthelmintic natural products from Hawaiian fungi

inferred← citeshttps://doi.org/10.1017/s0031182022000488openalex-snapshot

Host transmission dynamics of first- and third-stage Angiostrongylus cantonensis larvae in Bullastra lessoni

inferred← citeshttps://doi.org/10.1017/s0031182022001573openalex-snapshot

Genetic analysis of a 66-kDa protein-encoding gene of Angiostrongylus cantonensis and Angiostrongylus malaysiensis

inferred← citeshttps://doi.org/10.1017/s0031182025000034openalex-snapshot

Passage of Angiostrongylus cantonensis through the trophic web: an experimental study on reptiles

inferred← citeshttps://doi.org/10.1051/parasite/2018022openalex-snapshot

Angiostrongylus costaricensisinfection in Martinique, Lesser Antilles, from 2000 to 2017

inferred← citeshttps://doi.org/10.1051/parasite/2024069openalex-snapshot

Helminth diversity and seasonality of Angiostrongylus cantonensis in hedgehogs from Mallorca

inferred← citeshttps://doi.org/10.1071/ma25013openalex-snapshot

Neuroangiostrongyliasis: accidental zoonosis caused by the rat lungworm

inferred← citeshttps://doi.org/10.1071/zo19017openalex-snapshot

Wildlife parasitology in Australia: past, present and future

inferred← citeshttps://doi.org/10.1079/cabicompendium.30825openalex-snapshot

Limax maximus (leopard slug)

inferred← citeshttps://doi.org/10.1080/13235818.2025.2491040openalex-snapshot

Adapted methods for helminth detection reveal trematode and nematode infections in terrestrial molluscs of Sergipe State, Brazil

inferred← citeshttps://doi.org/10.1089/vbz.2020.2734openalex-snapshot

Genetic Characterization and Detection of Angiostrongylus cantonensis by Molecular Approaches

inferred← citeshttps://doi.org/10.1093/infdis/jiaf173openalex-snapshot

Rainfall- and Temperature-Driven Emergence of Neural Angiostrongyliasis in Eastern Australia, 2020–2024

inferred← citeshttps://doi.org/10.1093/med/9780198746690.003.0178openalex-snapshot

Angiostrongyliasis

inferred← citeshttps://doi.org/10.1101/2022.12.07.518866openalex-snapshot

Improving the detection of A. cantonensis in brain tissues of mammalian hosts

inferred← citeshttps://doi.org/10.1101/2022.12.19.521150openalex-snapshot

Angie-LAMP for diagnosis of human eosinophilic meningitis using dog as proxy: A LAMP assay for Angiostrongylus cantonensis DNA in cerebrospinal fluid

inferred← citeshttps://doi.org/10.1101/2025.04.10.25325607openalex-snapshot

Gastrointestinal parasites of zoonotic importance detected in bats in the conservation area of Semuliki National Park, western Uganda

inferred← citeshttps://doi.org/10.1111/1749-4877.12143openalex-snapshot

Global parasite and Rattus rodent invasions: The consequences for rodent‐borne diseases

inferred← citeshttps://doi.org/10.1111/1749-4877.12766openalex-snapshot

Physiological strategies in wild rodents: immune defenses of commensal rats

inferred← citeshttps://doi.org/10.1111/1749-4877.13004openalex-snapshot

Hedgehogs and Angiostrongylus cantonensis : Uncovering the Role of Atelerix albiventris in the Parasite Life Cycle

inferred← citeshttps://doi.org/10.1111/eva.12621openalex-snapshot

Hurdles in the evolutionary epidemiology of Angiostrongylus cantonensis: Pseudogenes, incongruence between taxonomy and DNA sequence variants, and cryptic lineages

inferred← citeshttps://doi.org/10.1111/zph.13072openalex-snapshot

A cross‐sectional study ofAngiostrongylus malaysiensisin rats and gastropod hosts from recreational parks in Kuala Lumpur, Malaysia: Detection, risk factors and pathology

inferred← citeshttps://doi.org/10.1128/cmr.00266-20openalex-snapshot

Canine and Feline Parasitology: Analogies, Differences, and Relevance for Human Health

inferred← citeshttps://doi.org/10.1155/japr/9972163openalex-snapshot

Gastrointestinal Parasites of Zoonotic Importance Detected in Bats in the Conservation Area of Semuliki National Park, Western Uganda

inferred← citeshttps://doi.org/10.11606/d.10.2024.tde-13032024-115326openalex-snapshot

>b /b<

inferred← citeshttps://doi.org/10.1177/10406387211037664openalex-snapshot

Verminous meningoencephalomyelitis in a red kangaroo associated with Angiostrongylus cantonensis infection

inferred← citeshttps://doi.org/10.1186/s12917-018-1494-0openalex-snapshot

Causes of mortality and morbidity in free-ranging mustelids in Switzerland: necropsy data from over 50 years of general health surveillance

inferred← citeshttps://doi.org/10.1186/s13071-015-1082-0openalex-snapshot

The mitochondrial genome of Angiostrongylus mackerrasae as a basis for molecular, epidemiological and population genetic studies

inferred← citeshttps://doi.org/10.1186/s13071-016-1440-6openalex-snapshot

Angiostrongylus vasorum in the eye: new case reports and a review of the literature

inferred← citeshttps://doi.org/10.1186/s13071-016-1483-8openalex-snapshot

Development of Crenosoma vulpis in the common garden snail Cornu aspersum: implications for epidemiological studies

inferred← citeshttps://doi.org/10.1186/s13071-016-1718-8openalex-snapshot

A rare cardiopulmonary parasite of the European badger, Meles meles: first description of the larvae, ultrastructure, pathological changes and molecular identification of Angiostrongylus daskalovi Janchev & Genov 1988

inferred← citeshttps://doi.org/10.1186/s13071-016-1961-zopenalex-snapshot

Gastropod-derived haemocyte extracellular traps entrap metastrongyloid larval stages of Angiostrongylus vasorum, Aelurostrongylus abstrusus and Troglostrongylus brevior

inferred← citeshttps://doi.org/10.1186/s13071-018-2765-0openalex-snapshot

Angiostrongylus vasorum and Aelurostrongylus abstrusus: Neglected and underestimated parasites in South America

inferred← citeshttps://doi.org/10.1186/s13071-019-3293-2openalex-snapshot

Mice as paratenic hosts of Aelurostrongylus abstrusus

inferred← citeshttps://doi.org/10.1186/s13071-025-06700-7openalex-snapshot

Living in the city: Angiostrongylus cantonensis is a novel threat to an urban population of Florida burrowing owls (Athene cunicularia floridana) in south Florida

inferred← citeshttps://doi.org/10.1292/jvms.21-0282openalex-snapshot

Pathologic features and molecular identification of parelaphostrongylosis in a sitatunga (Tragelaphus spekii)

inferred← citeshttps://doi.org/10.1371/journal.pntd.0005776openalex-snapshot

Phylogeography of Angiostrongylus cantonensis (Nematoda: Angiostrongylidae) in southern China and some surrounding areas

inferred← citeshttps://doi.org/10.1371/journal.pntd.0006923openalex-snapshot

Activity profiling of peptidases in Angiostrongylus costaricensis first-stage larvae and adult worms

inferred← citeshttps://doi.org/10.1371/journal.pntd.0007277openalex-snapshot

The invasive giant African snail Lissachatina fulica as natural intermediate host of Aelurostrongylus abstrusus, Angiostrongylus vasorum, Troglostrongylus brevior, and Crenosoma vulpis in Colombia

inferred← citeshttps://doi.org/10.1371/journal.pntd.0007846openalex-snapshot

The genetic basis of adaptive evolution in parasitic environment from the Angiostrongylus cantonensis genome

inferred← citeshttps://doi.org/10.1371/journal.pntd.0011038openalex-snapshot

Angie-LAMP for diagnosis of human eosinophilic meningitis using dog as proxy: A LAMP assay for Angiostrongylus cantonensis DNA in cerebrospinal fluid

inferred← citeshttps://doi.org/10.1371/journal.pntd.0013634openalex-snapshot

Hidden threats in urban environments: Angiostrongylus cantonensis in Banda Aceh’s cityscape

inferred← citeshttps://doi.org/10.1371/journal.pntd.0014024openalex-snapshot

Occurrence of Angiostrongylus cantonensis in invasive snails in the French territories of America, French Guiana, Guadeloupe, and Martinique

inferred← citeshttps://doi.org/10.1371/journal.pone.0134581openalex-snapshot

Mitochondrial Genome Supports Sibling Species of Angiostrongylus costaricensis (Nematoda: Angiostrongylidae)

inferred← citeshttps://doi.org/10.1371/journal.pone.0223257openalex-snapshot

Genetic characterization of Angiostrongylus larvae and their intermediate host, Achatina fulica, in Thailand

inferred← citeshttps://doi.org/10.1590/0001-3765202320220249openalex-snapshot

Diversity and abundance of terrestrial molluscs and their associated nematode fauna in urban kitchen gardens in the city of Rio de Janeiro, Brazil

inferred← citeshttps://doi.org/10.1590/0074-02760150371openalex-snapshot

New host, geographic records, and histopathologic studies ofAngiostrongylus spp (Nematoda: Angiostrongylidae) in rodents from Argentina with updated summary of records from rodent hosts and host specificity assessment

inferred← citeshttps://doi.org/10.1590/0074-02760170226openalex-snapshot

Angiostrongylus spp. in the Americas: geographical and chronological distribution of definitive hosts versus disease reports

inferred← citeshttps://doi.org/10.1590/0074-02760200236openalex-snapshot

Gastropods as intermediate hosts of Angiostrongylus spp. in the Americas: bioecological characteristics and geographical distribution

inferred← citeshttps://doi.org/10.1590/0103-8478cr20160547openalex-snapshot

Anatomo-pathological aspects of parasitism by nematodes of the superfamily Metastrongyloidea in wild crab-eating fox (Cerdocyon thous) in Midwestern Brazil

inferred← citeshttps://doi.org/10.1590/1678-4685-gmb-2016-0274openalex-snapshot

Comparative transcriptomic analysis of two important life stages of Angiostrongylus cantonensis: fifth-stage larvae and female adults

inferred← citeshttps://doi.org/10.1590/1678-5150-pvb-7666openalex-snapshot

Anatomopathological findings and causes of death in wild canids rescued in São Paulo State (2021-2023): implications for wildlife health and conservation

inferred← citeshttps://doi.org/10.1590/s1984-29612019103openalex-snapshot

Angiostrongylus minasensis n. sp.: new species found parasitizing coatis (Nasua nasua) in an urban protected area in Brazil

inferred← citeshttps://doi.org/10.1590/s1984-29612021058openalex-snapshot

Rodent helminths in fragmented Atlantic Forest areas in the western region of the state of Paraná

inferred← citeshttps://doi.org/10.1645/18-176openalex-snapshot

The Occurrence of Physaloptera Hispida and a Mastophorus Sp. in Pulmonary Vessels of Hispid Cotton Rats ( Sigmodon hispidus) from Georgia, U.S.A.

inferred← citeshttps://doi.org/10.21203/rs.3.rs-37815/v1openalex-snapshot

SYBR-Green-Based Quantitative Real-Time PCR for Discriminating Between Closely Related Angiostrongylus Cantonensis and A. Malaysisensis

inferred← citeshttps://doi.org/10.21203/rs.3.rs-6424431/v1openalex-snapshot

Gastrointestinal parasites of zoonotic importance detected in bats in the conservation area of Semuliki National Park, western Uganda

inferred← citeshttps://doi.org/10.2298/vetgl170310010iopenalex-snapshot

Cardiopulmonary metastrongyloidosis of dogs and cats contribution to diagnose

inferred← citeshttps://doi.org/10.2298/vetgl2001085sopenalex-snapshot

First report of autochthonous canine angiostrongylosis in Bosnia and Herzegovina

inferred← citeshttps://doi.org/10.24070/bjvp.1983-0246.018001openalex-snapshot

Angiostrongylus spp. in the nasal mucosa of Didelphis sp

inferred← citeshttps://doi.org/10.2478/macvetrev-2025-0029openalex-snapshot

Morphological and Genetic Diversity of Angiostrongylus vasorum

inferred← citeshttps://doi.org/10.2478/s11686-019-00029-9openalex-snapshot

Severe Verminous Pneumonia Caused by Natural Mixed Infection with Aelurostrongylus abstrusus and Angiostrongylus chabaudi in a European Wildcat from Western Balkan Area

inferred← citeshttps://doi.org/10.26077/aqtz-a113openalex-snapshot

A Review of Rat Lungworm Infection and Recent Data on Its Definitive Hosts in Hawaii

inferred← citeshttps://doi.org/10.2754/avb201988030303openalex-snapshot

Co-infection with Angiostrongylus chabaudi and Dirofilaria immitis in a wildcat, Felis silvestris from Romania – a case report

inferred← citeshttps://doi.org/10.2807/1560-7917.es.2019.24.33.1900489openalex-snapshot

Angiostrongylus cantonensis in North African hedgehogs as vertebrate hosts, Mallorca, Spain, October 2018

inferred← citeshttps://doi.org/10.2984/79.2.2openalex-snapshot

Reexamination of Rat Lungworm (Angiostrongylus cantonensis: Nematoda) Prevalence in Wild Rattus spp. on the Island of Kaua‘i after a 60-Year Hiatus1

inferred← citeshttps://doi.org/10.3201/eid2412.180056openalex-snapshot

Rat Lungworm Infection in Rodents across Post-Katrina New Orleans, Louisiana, USA

inferred← citeshttps://doi.org/10.33448/rsd-v11i4.26637openalex-snapshot

Gastrointestinal parasites in captive wild animals from two Brazilian Zoological Gardens

inferred← citeshttps://doi.org/10.3347/kjp.2015.53.6.713openalex-snapshot

A Case of Ocular Angiostrongyliasis with Molecular Identification of the Species in Vietnam

inferred← citeshttps://doi.org/10.3389/fpara.2026.1797945openalex-snapshot

Case Report: Neurological and pulmonary angiostrongylosis in a Ryukyu long-furred rat (Diplothrix legata) on Amami-Oshima Island, Japan

inferred← citeshttps://doi.org/10.3389/fvets.2022.1023426openalex-snapshot

Parasitism of terrestrial gastropods by medically-important nematodes in Brazil

inferred← citeshttps://doi.org/10.3389/fvets.2024.1294484openalex-snapshot

Case report: First documented case of cerebral angiostrongyliasis caused by Angiostrongylus costaricensis in a free-ranging opossum

inferred← citeshttps://doi.org/10.3390/d15050611openalex-snapshot

First Worldwide Evidence of Bronchopulmonary Strongyle Nematodes and the First Report on Italy of Cryptosporidium sp. in Allochthonous Nutria (Myocastor coypus)

inferred← citeshttps://doi.org/10.3390/microorganisms10081565openalex-snapshot

Nationwide Seroprevalence Survey of Angiostrongylus vasorum-Derived Antigens and Specific Antibodies in Dogs from Colombia

inferred← citeshttps://doi.org/10.3390/pathogens10060715openalex-snapshot

Habitat Characteristics as Potential Drivers of the Angiostrongylus daskalovi Infection in European Badger (Meles meles) Populations

inferred← citeshttps://doi.org/10.3390/pathogens10101236openalex-snapshot

Angiostrongylosis in Animals and Humans in Europe

inferred← citeshttps://doi.org/10.3390/pathogens12040567openalex-snapshot

Update on the First Finding of the Rat Lungworm, Angiostrongylus cantonensis, in Rattus spp. in Continental Europe, Valencia, Spain, 2022

inferred← citeshttps://doi.org/10.3390/pathogens13030255openalex-snapshot

The Zoonotic Angiostrongylus cantonensis and the Veterinary Parasite Aelurostrongylus abstrusus Infecting Terrestrial Gastropods from Urban Areas of Macapá, Brazilian Amazon Region

inferred← citeshttps://doi.org/10.3390/pathogens15070757openalex-snapshot

Detection of Aelurostrongylus spp. Infection in the Neozoan American Mink (Neogale vison) in Southern Chile

inferred← citeshttps://doi.org/10.35537/10915/65717openalex-snapshot

Epidemiología de las parasitosis transmitidas por moluscos en el NE de Argentina: Puerto Iguazú, sitio de intercambio en la triple frontera

inferred← citeshttps://doi.org/10.35841/biomedicalresearch.30-19-134openalex-snapshot

Analyses of single nucleotide polymorphisms in Angiostrongylus cantonensis based on transcriptome sequencing.

inferred← citeshttps://doi.org/10.4103/ijo.ijo_843_18openalex-snapshot

Angiostrongylus cantonensis in anterior chamber

inferred← citeshttps://doi.org/10.5005/jacm-11020-0029openalex-snapshot

Eosinophilic Meningitis due to Angiostrongylus cantonensis: A Rare Brain Intruder in Infants

inferred← citeshttps://doi.org/10.5216/rpt.v45i1.40272openalex-snapshot

EVALUATION OF TECHNIQUES FOR RECOVERY OF Angiostrongylus vasorum FROM Achatina fulica, A POTENTIAL INTERMEDIATE HOST

inferred← citeshttps://doi.org/10.56238/connexpemultidisdevolpfut-100openalex-snapshot

Tools for control of the african snail (Achatina fulica, Bowdich, 1822)

inferred← citeshttps://doi.org/10.70675/fac094eaz765ez483fz9078zfc3f7882d14copenalex-snapshot

Identification et caractérisation de BCLA, un antigène spécifique du stade kystique de Toxoplasma gondii et marqueur sérologique potentiel des toxoplasmoses latentes

inferred← citeshttps://doi.org/10.7589/2018-12-294openalex-snapshot

Occurrence of Rat Lungworm (Angiostrongylus cantonensis) in Invasive Coqui Frogs (Eleutherodactylus coqui) and Other Hosts in Hawaii, USA

inferred← citeshttps://doi.org/10.7705/biomedica.v39i3.4387openalex-snapshot

Angiostrongylus (Parastrongylus) cantonensis en huéspedes intermediarios y definitivos en Ecuador, 2014-2017

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