Drug treatment and novel drug target against Cryptosporidium
Parasite, 15 3 (2008) 275-281
Published online: 2008-09-15
Articles citing this article
The Citing articles tool gives a list of articles citing the current article.
The citing articles come from EDP Sciences database, as well as other publishers participating in CrossRef Cited-by Linking Program. You can set up your personal account to receive an email alert each time this article is cited by a new article (see the menu on the right-hand side of the abstract page).
Cited article:
This article has been cited by the following article(s):
Parasitic protozoa: Biosystematics, identification, pathogenicity, causes and remedial measures
Gourav Mishra, Razia Kausar and Tushar YadavMicrobial Pathogenesis 207 107867 (2025)
https://doi.org/10.1016/j.micpath.2025.107867
Efficacy of Lactobacillus taiwanensis S29 and Lactiplantibacillus plantarum S27 against tapeworm infection in Swiss Albino rats
Sudeshna Mandal, Chandrani Mondal, Sinchan Ghosh, Samiparna Saha, Mou Singha Ray and Larisha M. LyndemExperimental Parasitology 259 108715 (2024)
https://doi.org/10.1016/j.exppara.2024.108715
Herbal-based compounds: A review on treatments of cryptosporidiosis
Fatemeh Namazi and Seyed Mostafa RazaviInternational Journal for Parasitology: Drugs and Drug Resistance 24 100521 (2024)
https://doi.org/10.1016/j.ijpddr.2024.100521
Pharmacokinetics and tissue distribution of LN002, a new compound alternative oxidase inhibitor against Cryptosporidium in rats
Minglang Ma, Yongxiang Zhang, Yanjun Fang, Yixing Lu, Huiguo Huang, Zhenling Zeng and Dongping ZengFrontiers in Pharmacology 15 (2024)
https://doi.org/10.3389/fphar.2024.1413872
miR-181d targets BCL2 to regulate HCT-8 cell apoptosis and parasite burden in response to Cryptosporidium parvum infection via the intrinsic apoptosis pathway
Juanfeng Li, Ruiying Feng, Xiaotian Zhang, Wenyan Hou, Yingying Zhang, Junqiang Li, Xiaoying Li, Fuchun Jian, Longxian Zhang, Sumei Zhang and Rongjun WangVeterinary Parasitology 330 110237 (2024)
https://doi.org/10.1016/j.vetpar.2024.110237
The first commercially approved efficacious cryptosporidium vaccine protecting New-Born calves from severe diarrhea
Marina Timmermans, Willem Hubers, Dianne Schroer, Koen Gevers, Ruud PAM Segers, Ron Niessen and Mark H van RoosmalenVeterinary Vaccine 3 (1) 100054 (2024)
https://doi.org/10.1016/j.vetvac.2024.100054
A multi-epitope vaccine candidate developed from unique immunogenic epitopes against Cryptosporidium hominis by utilizing an immunoinformatics-driven approach
Nirali Pandya and Amit KumarJournal of Biomolecular Structure and Dynamics 41 (10) 4614 (2023)
https://doi.org/10.1080/07391102.2022.2070284
Therapeutic efficacy of proton pump inhibitor (omeprazole) on cryptosporidiosis parvum in immunosuppressed experimental mice
Engy V. N. Beshay, Nashaat E. Nassef, Omaima K. El Shafei, Mona M. Saleh, Mona A. Kora and Fatma H. ShalaanJournal of Parasitic Diseases 47 (3) 535 (2023)
https://doi.org/10.1007/s12639-023-01592-9
Cost-effective In Vivo and In Vitro Mouse Models for Evaluating Anticryptosporidial Drug Efficacy: Assessing Vorinostat, Docetaxel, and Baicalein
Mingxiao Liu, Di Zhang, Dongqiang Wang, Xiaodong Wu, Ying Zhang, Jigang Yin and Guan ZhuThe Journal of Infectious Diseases 228 (10) 1430 (2023)
https://doi.org/10.1093/infdis/jiad243
The potential therapeutic effect of Nigella sativa and Zingiber officinale extracts versus Nitazoxanide drug against experimentally induced cryptosporidiosis in laboratory mice
Samah Hassan Yahia, Reda Lamei El gamal, Ghada Mahmoud Fathy, et al.Journal of Parasitic Diseases 47 (2) 329 (2023)
https://doi.org/10.1007/s12639-023-01572-z
Evaluation of the therapeutic efficacy of some essential oils in experimentally immunosuppressed mice infected with Cryptosporidium parvum
Noha Madbouly Taha, Rabab Sayed Zalat, Eman Khaled and Basma M. ElmansoryJournal of Parasitic Diseases 47 (4) 733 (2023)
https://doi.org/10.1007/s12639-023-01621-7
(2023)
https://doi.org/10.21203/rs.3.rs-2436725/v1
Investigation of the prophylactic and therapeutic effectiveness of oral thyme extract in rats experimentally infected with cryptosporidium parvum
Erdal Kara, Sibel Yasa Duru, Sami Gökpinar, Özkan Duru, Sedat Sevin, Yasin Şenel and Ufuk KayaVeterinary Research Communications 47 (2) 663 (2023)
https://doi.org/10.1007/s11259-022-10025-6
Therapeutic Potency of Ginger, Garlic, and Pomegranate Extracts Against Cryptosporidium parvum-Mediated Gastro-Splenic Damage in Mice
Dina M. M. EL-Shewehy, Gehad E. Elshopakey, Amira Ismail, Shimaa S. Hassan and Amany M. RamezActa Parasitologica 68 (1) 32 (2023)
https://doi.org/10.1007/s11686-022-00635-0
Pathobiology of Parasitic Protozoa: Dynamics and Dimensions
Amresh Kumar Singh, Suraiya Khanam Ansari, Alok Raghav and Vivek GaurPathobiology of Parasitic Protozoa: Dynamics and Dimensions 45 (2023)
https://doi.org/10.1007/978-981-19-8225-5_3
Bioactive Peptides against Human Apicomplexan Parasites
Norma Rivera-Fernández, Jhony Anacleto-Santos, Brenda Casarrubias-Tabarez, Teresa de Jesús López-Pérez, Marcela Rojas-Lemus, Nelly López-Valdez and Teresa I. FortoulAntibiotics 11 (11) 1658 (2022)
https://doi.org/10.3390/antibiotics11111658
QSAR and deep learning model for virtual screening of potential inhibitors against Inosine 5’ Monophosphate dehydrogenase (IMPDH) of Cryptosporidium parvum
Misgana Mengistu Asmare, Nitin Nitin, Soon-IL Yun and Rajani Kanta MahapatraJournal of Molecular Graphics and Modelling 111 108108 (2022)
https://doi.org/10.1016/j.jmgm.2021.108108
Parasitic Helminths and Zoonoses - From Basic to Applied Research
Osama M. Darwesh and Hoda Samir El-SayedParasitic Helminths and Zoonoses - From Basic to Applied Research (2022)
https://doi.org/10.5772/intechopen.103744
Anti-cryptosporidial activity of Camellia sinensis (green tea extract) in experimentally infected immunocompromised mice
Eman S. El-Wakil, Eman Ali Mohamed, Eman Ahmed El-Wakil, Tarek S. AbouShousha and Neimat Mousa AmerActa Protozoologica 61 23 (2022)
https://doi.org/10.4467/16890027AP.22.002.16205
Efficacy of clofazimine and nitazoxanide combination in treating intestinal cryptosporidiosis and enhancing intestinal cellular regeneration in immunocompromised mice
Marwa Esmat, Amany A. Abdel-Aal, Maisa A. Shalaby, Manal Badawi, Hala Elaskary, Ahmed Badawi Yousif and Mennat-Elrahman A. FahmyFood and Waterborne Parasitology 27 e00161 (2022)
https://doi.org/10.1016/j.fawpar.2022.e00161
Garlic (Allium sativum Linnaeus) improved inflammation and reduced cryptosporidiosis burden in immunocompromised mice
Alyaa Farid, Mona Yousry and Gehan SafwatJournal of Ethnopharmacology 292 115174 (2022)
https://doi.org/10.1016/j.jep.2022.115174
In vivo evaluation of anticryptosporidial effects of wheat germ extracts in immunocompromised mice
Hagar F. Abdelmaksoud, Ezzat E. A. Osman, Sayed S. Abdel-Hameed, Tarek Aboushousha and Heba M. El NaggarJournal of Parasitic Diseases 46 (3) 833 (2022)
https://doi.org/10.1007/s12639-022-01502-5
Chemical profiling of Verbena officinalis and assessment of its anti-cryptosporidial activity in experimentally infected immunocompromised mice
Eman S. El-Wakil, Maha A.M. El-Shazly, Ayman M. El-Ashkar, Tarek Aboushousha and Mosad A. GhareebArabian Journal of Chemistry 15 (7) 103945 (2022)
https://doi.org/10.1016/j.arabjc.2022.103945
1285 (2021)
https://doi.org/10.1016/B978-0-323-50934-3.00103-8
The Efficacy of Citrus maxima Peels Aqueous Extract Against Cryptosporidiosis in Immunecompromised Mice
Eman Naser Hafez and Wafaa Fayez Abd El HamedActa Parasitologica 66 (2) 638 (2021)
https://doi.org/10.1007/s11686-020-00315-x
Emerging Trends in Nanomedicine
Riti Mehta and Souvik SenguptaEmerging Trends in Nanomedicine 203 (2021)
https://doi.org/10.1007/978-981-15-9920-0_7
Giardia and Cryptosporidium in Neo-Tropical Rodents and Marsupials: Is There Any Zoonotic Potential?
Kegan Romelle Jones and Laura TardieuLife 11 (3) 256 (2021)
https://doi.org/10.3390/life11030256
Persistent Cryptosporidium parvum Infection Leads to the Development of the Tumor Microenvironment in an Experimental Mouse Model: Results of a Microarray Approach
Manasi Sawant, Sadia Benamrouz-Vanneste, Anthony Mouray, Peggy Bouquet, Nausicaa Gantois, Colette Creusy, Erika Duval, Adriana Mihalache, Pierre Gosset, Magali Chabé, David Hot, Eric Viscogliosi and Gabriela CertadMicroorganisms 9 (12) 2569 (2021)
https://doi.org/10.3390/microorganisms9122569
Evaluation of possible prophylactic and therapeutic effect of mefloquine on experimental cryptosporidiosis in immunocompromised mice
Eman S. El-Wakil, Amal E. Salem and Asmaa M. F. Al-GhandourJournal of Parasitic Diseases 45 (2) 380 (2021)
https://doi.org/10.1007/s12639-020-01315-4
The immunomodulatory activity of secnidazole–nitazoxanide in a murine cryptosporidiosis model
Neveen Madbouly, Azza El Amir, Asmaa Abdel Kader, Ibraheem Rabee and Alyaa FaridJournal of Medical Microbiology 70 (3) (2021)
https://doi.org/10.1099/jmm.0.001327
S-Methylcysteine (SMC) Ameliorates Intestinal, Hepatic, and Splenic Damage Induced by Cryptosporidium parvum Infection Via Targeting Inflammatory Modulators and Oxidative Stress in Swiss Albino Mice
Ehab Kotb Elmahallawy, Gehad E. Elshopakey, Amira A. Saleh, Ahmad Agil, Ahmed El-Morsey, Dina M. M. EL-shewehy, Ahmed S. Sad, Tokuma Yanai and Walied AbdoBiomedicines 8 (10) 423 (2020)
https://doi.org/10.3390/biomedicines8100423
Potential therapeutic and prophylactic effects of Asafoetida in murine cryptosporidiosis
Hagar F. Abdelmaksoud, Ayman M. El-Ashkar, Sh. A. Elgohary and Eman S. El-WakilJournal of Parasitic Diseases 44 (3) 646 (2020)
https://doi.org/10.1007/s12639-020-01241-5
Parasitology and Microbiology Research
Helena Lúcia Carneiro Santos, Karina Mastropasqua Rebello and Teresa Cristina Bergamo BomfimParasitology and Microbiology Research (2020)
https://doi.org/10.5772/intechopen.88387
Etiological Treatment of Protozoer Diarrhea in Neonatal Ruminants
İlker Yusuf AKINCI and Metin Koray ALBAYVeterinary Journal of Mehmet Akif Ersoy University 5 (1) 28 (2020)
https://doi.org/10.24880/maeuvfd.681052
Oocysticidal Effect of Essential Oils (EOs) and their Major Components on Cryptosporidium baileyi and Cryptosporidium galli
M. Tanghort, H. Chefchaou, A. Mzabi, et al.International Journal of Poultry Science 18 (10) 475 (2019)
https://doi.org/10.3923/ijps.2019.475.482
Limitations in the screening of potentially anti-cryptosporidial agents using laboratory rodents with gastric cryptosporidiosis
Andrea Valigurova, Radka Peckova, Karel Dolezal, et al.Folia Parasitologica 65 (2018)
https://doi.org/10.14411/fp.2018.010
The anti-parasitic effect of probiotic bacteria via limiting the fecundity of Trichinella spiralis female adults
B. Bucková, Z. Hurníková, A. Lauková, V. Revajová and E. DvorožňákováHelminthologia 55 (2) 102 (2018)
https://doi.org/10.2478/helm-2018-0010
Effect of oregano essential oil and carvacrol on Cryptosporidium parvum infectivity in HCT-8 cells
Shashank Gaur, Theresa B. Kuhlenschmidt, Mark S. Kuhlenschmidt and Juan E. AndradeParasitology International 67 (2) 170 (2018)
https://doi.org/10.1016/j.parint.2017.11.001
Cryptosporidiosis: A zoonotic disease concern
Natapol Pumipuntu and Supawadee PirataeVeterinary World 11 (5) 681 (2018)
https://doi.org/10.14202/vetworld.2018.681-686
Public health significance of zoonotic Cryptosporidium species in wildlife: Critical insights into better drinking water management
Alireza Zahedi, Andrea Paparini, Fuchun Jian, Ian Robertson and Una RyanInternational Journal for Parasitology: Parasites and Wildlife 5 (1) 88 (2016)
https://doi.org/10.1016/j.ijppaw.2015.12.001
Cryptosporidium canis in Two Mexican Toddlers
Mariana González-Díaz, Alejandro Urrea-Quezada, Isaac Villegas-Gómez, et al.Pediatric Infectious Disease Journal 35 (11) 1265 (2016)
https://doi.org/10.1097/INF.0000000000001287
Manual ofClinical Microbiology
Lihua Xiao and Vitaliano CamaManual ofClinical Microbiology 2435 (2015)
https://doi.org/10.1128/9781555817381.ch142
Parasitic diarrheal disease: drug development and targets
Amir Azam, Mudasir N. Peerzada and Kamal AhmadFrontiers in Microbiology 6 (2015)
https://doi.org/10.3389/fmicb.2015.01183
Target validation of the inosine monophosphate dehydrogenase (IMPDH) gene in Cryptosporidium using Phylomer® peptides
R. Jefferies, R. Yang, C.K. Woh, et al.Experimental Parasitology 148 40 (2015)
https://doi.org/10.1016/j.exppara.2014.11.003
Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases
David A. Bobak and Richard L. GuerrantMandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases 1253 (2015)
https://doi.org/10.1016/B978-1-4557-4801-3.00100-4
Validation of cell-free culture using scanning electron microscopy (SEM) and gene expression studies
R. Yang, Y. Elankumaran, N. Hijjawi and U. RyanExperimental Parasitology 153 55 (2015)
https://doi.org/10.1016/j.exppara.2015.03.002
Update on the role of cryptosporidiosis in calf diarrhoea
Emily Hotchkiss, Sarah Thomson, Beth Wells, Elisabeth Innes and Frank KatzerLivestock 20 (6) 316 (2015)
https://doi.org/10.12968/live.2015.20.6.316
Manual of Security Sensitive Microbes and Toxins
Lihua Xiao and Yaoyu FengManual of Security Sensitive Microbes and Toxins 427 (2014)
https://doi.org/10.1201/b16752-42
Genomes of Foodborne and Waterborne Pathogens
Guan Zhu and Lihua XiaoGenomes of Foodborne and Waterborne Pathogens 271 (2014)
https://doi.org/10.1128/9781555816902.ch19
Infectivity of Cryptosporidium andersoni and Cryptosporidium muris to Normal and Immunosuppressive Cynomolgus Monkeys
Koichi MASUNO, Yasuhiro FUKUDA, Masahito KUBO, et al.Journal of Veterinary Medical Science 76 (2) 169 (2014)
https://doi.org/10.1292/jvms.13-0350
Cryptosporidium parvum has an active hypusine biosynthesis pathway
Nimisha Mittal, Marie Morada, Pankaj Tripathi, et al.Molecular and Biochemical Parasitology 195 (1) 14 (2014)
https://doi.org/10.1016/j.molbiopara.2014.05.005
An evaluation of the potential use of Cryptosporidium species as agents for deliberate release
Ralf Matthias Hagen, U Loderstaedt and H FrickmannJournal of the Royal Army Medical Corps 160 (4) 289 (2014)
https://doi.org/10.1136/jramc-2013-000186
Canine and Feline Infectious Diseases
Michael R. LappinCanine and Feline Infectious Diseases 785 (2014)
https://doi.org/10.1016/B978-1-4377-0795-3.00081-8
Role of COX-2 in Pathogenesis of Intestinal Cryptosporidiosis and Effect of some Drugs on Treatment of Infection
Gehan S. Sadek and Bahaa El Deen W. El AswaResearch Journal of Parasitology 9 (2) 21 (2014)
https://doi.org/10.3923/jp.2014.21.40
CDPKs of Cryptosporidium parvum—stage-specific expression in vitro
Manja Etzold, Matthias Lendner, Arwid Daugschies and Viktor DyachenkoParasitology Research 113 (7) 2525 (2014)
https://doi.org/10.1007/s00436-014-3902-0
Food Associated Pathogens
Lucy RobertsonFood Associated Pathogens 169 (2013)
https://doi.org/10.1201/b15475-14
Effect of Nitaxozanide and Pyrimethamine on Astrocytes Infected by Toxoplasma gondii In Vitro
Ma. de la Luz Galván-Ramírez, Judith Marcela Dueñas Jiménez, Laura Rocío Rodríguez Pérez, Rogelio Troyo-Sanroman, Mario Ramírez-Herrera and Trinidad García-IglesiasArchives of Medical Research 44 (6) 415 (2013)
https://doi.org/10.1016/j.arcmed.2013.07.002
Diarrhea
Aaron C. Hamilton and Moises AuronHospital Medicine Clinics 2 (2) e227 (2013)
https://doi.org/10.1016/j.ehmc.2012.12.002
Assessment of Cryptosporidium parvum infection in immunocompetent and immunocompromised mice and its role in triggering intestinal dysplasia
Asmaa Gaber Abdou, Nancy Mahmoud Harba, Amira Fathy Afifi and Nada Farag ElnaidanyInternational Journal of Infectious Diseases 17 (8) e593 (2013)
https://doi.org/10.1016/j.ijid.2012.11.023
Cryptosporidiosis as threatening health problem: A review
Nurul Fariza Rossle and Baha LatifAsian Pacific Journal of Tropical Biomedicine 3 (11) 916 (2013)
https://doi.org/10.1016/S2221-1691(13)60179-3
Pathological features of Cryptosporidium andersoni-induced lesions in SCID mice
Koichi Masuno, Tokuma Yanai, Hiroki Sakai, et al.Experimental Parasitology 134 (3) 381 (2013)
https://doi.org/10.1016/j.exppara.2013.02.006
Traitement des parasitoses digestives (amœbose exclue)
G. Cinquetti, M.-P. Massoure and P. ReyEMC - Gastro-entérologie 30 (1) 1 (2013)
https://doi.org/10.1016/S1155-1968(13)50490-1
Canine and Feline Gastroenterology
Canine and Feline Gastroenterology 651 (2013)https://doi.org/10.1016/B978-1-4160-3661-6.00057-2
Therapy and prevention of cryptosporidiosis in animals
Md. Shahiduzzaman and Arwid DaugschiesVeterinary Parasitology 188 (3-4) 203 (2012)
https://doi.org/10.1016/j.vetpar.2012.03.052
Traitement des parasitoses digestives (amœbose exclue)
G. Cinquetti, M.-P. Massoure and P. ReyEMC - Maladies infectieuses 29 (1) 1 (2012)
https://doi.org/10.1016/S1166-8598(12)54709-5
Nitazoxanide suppresses IL-6 production in LPS-stimulated mouse macrophages and TG-injected mice
Seong Keun Hong, Hee Joo Kim, Chang Seon Song, et al.International Immunopharmacology 13 (1) 23 (2012)
https://doi.org/10.1016/j.intimp.2012.03.002
Efficacy ofAllium sativum(garlic) against experimental cryptosporidiosis
Maha Reda GaafarAlexandria Journal of Medicine 48 (1) 59 (2012)
https://doi.org/10.1016/j.ajme.2011.12.003
Current and Evolving Clinical Options for HIV-Infected Patients with Chronic Diarrhoea
Tom Wingfield, Ashley Pennell and Tom J. BlanchardClinical Medicine Insights: Therapeutics 3 (2011)
https://doi.org/10.4137/CMT.S6386
3 (2011)
https://doi.org/10.1002/9780470958957.ch1
A Rapid, High-Throughput Viability Assay for Blastocystis spp. Reveals Metronidazole Resistance and Extensive Subtype-Dependent Variations in Drug Susceptibilities
Haris Mirza, Joshua D. W. Teo, Jacqui Upcroft and Kevin S. W. TanAntimicrobial Agents and Chemotherapy 55 (2) 637 (2011)
https://doi.org/10.1128/AAC.00900-10
Manual of Clinical Microbiology
Lihua Xiao and Vitaliano CamaManual of Clinical Microbiology 2180 (2011)
https://doi.org/10.1128/9781555816728.ch139
Structure of triosephosphate isomerase fromCryptosporidium parvum
Trang N. Nguyen, Jan Abendroth, David J. Leibly, et al.Acta Crystallographica Section F Structural Biology and Crystallization Communications 67 (9) 1095 (2011)
https://doi.org/10.1107/S1744309111019178
Probiotics for the Control of Parasites: An Overview
Marie-Agnès Travers, Isabelle Florent, Linda Kohl and Philippe GrellierJournal of Parasitology Research 2011 1 (2011)
https://doi.org/10.1155/2011/610769
Antibody responses following administration of a Cryptosporidium parvum rCP15/60 vaccine to pregnant cattle
A.J. Burton, D.V. Nydam, G. Jones, et al.Veterinary Parasitology 175 (1-2) 178 (2011)
https://doi.org/10.1016/j.vetpar.2010.09.013
The loading of labelled antibody-engineered nanoparticles with Indinavir increases itsin vitroefficacy againstCryptosporidium parvum
L. BONDIOLI, A. LUDOVISI, G. TOSI, et al.Parasitology 138 (11) 1384 (2011)
https://doi.org/10.1017/S0031182011001119
Cryptosporidium-Malnutrition Interactions: Mucosal Disruption, Cytokines, and TLR Signaling In A Weaned Murine Model
Lourrany B Costa, Eric A JohnBull, Jordan T Reeves, et al.Journal of Parasitology 97 (6) 1113 (2011)
https://doi.org/10.1645/GE-2848.1
Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases
DAVID A. BOBAK and RICHARD L. GUERRANTMandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases 1359 (2010)
https://doi.org/10.1016/B978-0-443-06839-3.00095-3
Complete development and multiplication of Cryptosporidium hominis in cell-free culture
Nawal Hijjawi, Annika Estcourt, Rongchang Yang, Paul Monis and Una RyanVeterinary Parasitology 169 (1-2) 29 (2010)
https://doi.org/10.1016/j.vetpar.2009.12.021
Update on the Diagnosis and Management of Cryptosporidium spp Infections in Dogs and Cats
Valeria Scorza and Sahatchai TangtrongsupTopics in Companion Animal Medicine 25 (3) 163 (2010)
https://doi.org/10.1053/j.tcam.2010.07.007
Triazole Inhibitors of Cryptosporidium parvum Inosine 5′-Monophosphate Dehydrogenase
Sushil K. Maurya, Deviprasad R. Gollapalli, Shivapriya Kirubakaran, et al.Journal of Medicinal Chemistry 52 (15) 4623 (2009)
https://doi.org/10.1021/jm900410u
Functional Expression of a DNA‐Topoisomerase IB from Cryptosporidium parvum
César Ordóñez, Javier Alfonso, Rafael Balaña-Fouce, David Ordóñez and Ali OuaissiBioMed Research International 2009 (1) (2009)
https://doi.org/10.1155/2009/837608
Genetic polymorphism in Cryptosporidium species: An update
Judit Plutzer and Panagiotis KaranisVeterinary Parasitology 165 (3-4) 187 (2009)
https://doi.org/10.1016/j.vetpar.2009.07.003