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"ITS1"

Original Article

Morphological and Molecular Identification of Spirometra Tapeworms (Cestoda: Diphyllobothriidae) from Carnivorous Mammals in the Serengeti and Selous Ecosystems of Tanzania
Barakaeli Abdieli Ndosi, Hansol Park, Dongmin Lee, Seongjun Choe, Yeseul Kang, Tilak Chandra Nath, Mohammed Mebarek Bia, Chatanun Eamudomkarn, Hyeong-Kyu Jeon, Keeseon S. Eom
Korean J Parasitol 2020;58(6):653-660.
Published online December 29, 2020
DOI: https://doi.org/10.3347/kjp.2020.58.6.653
Spirometra tapeworms (Cestoda: Diphyllobothriidae) collected from carnivorous mammals in Tanzania were identified by the DNA sequence analysis of the mitochondrial cytochrome c oxidase subunit 1 (cox1) and internal transcribed spacer 1 (ITS1), and by morphological characteristics. A total of 15 adult worms were collected from stool samples and carcasses of Panthera leo, Panthera pardus, and Crocuta crocuta in the Serengeti and Selous ecosystems of Tanzania. Three Spirometra species: S. theileri, S. ranarum and S. erinaceieuropaei were identified based on morphological features. Partial cox1 sequences (400 bp) of 10 specimens were revealed. Eight specimens showed 99.5% similarity with Spirometra theileri (MK955901), 1 specimen showed 99.5% similarity with the Korean S. erinaceieuropaei and 1 specimen had 99.5% similarity with Myanmar S. ranarum. Sequence homology estimates for the ITS1 region of S. theileri were 89.8% with S. erinaceieuropaei, 82.5% with S. decipiens, and 78.3% with S. ranarum; and 94.4% homology was observed between S. decipiens and S. ranarum. Phylogenetic analyses were performed with 4 species of Spirometra and 2 species of Dibothriocephalus (=Diphyllobothrium). By both ML and BI methods, cox1 and ITS1 gave well supported, congruent trees topology of S. erinaceieuropaei and S. theileri with S. decipiens and S. ranarum forming a clade. The Dibothriocephalus species were sisters of each other and collectively forming successive outgroups. Our findings confirmed that 3 Spirometra species (S. theileri, S. ranarum, and S. erinaceieuropaei) are distributed in the Serengeti and Selous ecosystems of Tanzania.

Citations

Citations to this article as recorded by  Crossref logo
  • Molecular confirmation of Spirometra mansoni (Cestoda: Diphyllobothriidae) in Javanese keelback water snake (Fowlea melanzosta) in Indonesia
    Ryanka Edila, Seongjun Choe, Mustofa Helmi Effendi, Lucia Tri Suwanti, John Yew Huat Tang
    International Journal for Parasitology: Parasites and Wildlife.2025; 28: 101150.     CrossRef
  • Description of Spirometra asiana sp. nov. (Cestoda: Diphyllobothriidae) found in wild boars and hound dogs in Japan
    Hiroshi Yamasaki, Hiromu Sugiyama, Yasuyuki Morishima, Hirotaka Kobayashi
    Parasitology International.2024; 98: 102798.     CrossRef
  • Molecular Characterization of Spirometra erinaceieuropaei from Jungle Cat (Felis chaus) in North of Iran
    Mahboobeh Salimi, Meysam Sharifdini, Eshrat Beigom Kia
    Acta Parasitologica.2024; 69(1): 574.     CrossRef
  • Diversity and biology of Spirometra tapeworms (Cestoda: Diphyllobothriidea), zoonotic parasites of wildlife: A review
    Roman Kuchta, Anna J. Phillips, Tomáš Scholz
    International Journal for Parasitology: Parasites and Wildlife.2024; 24: 100947.     CrossRef
  • Mitochondrial Genome of Spirometra theileri Compared with Other Spirometra Species
    Barakaeli Abdieli Ndosi, Hansol Park, Dongmin Lee, Seongjun Choe, Yeseul Kang, Tilak Chandra Nath, Mohammed Mebarek Bia, Chatanun Eamudomkarn, Hyeong-Kyu Jeon, Keeseon S. Eom
    The Korean Journal of Parasitology.2021; 59(2): 139.     CrossRef
  • 5,106 View
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  • 5 Web of Science
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Case Report

Ten Cases of Taenia saginata Infection Confirmed by Analysis of the Internal Transcribed Spacer 1 rDNA Region in the Republic of Korea
Su-Min Song, Hae Soo Yun, Dorene VanBik, Hyun-Ha Chang, Sang-Ah Lee, Shin-Woo Kim, Namhee Ryoo, Dong Yeub Eun, Nan Young Lee, Youn-Kyoung Goo, Yeonchul Hong, Meesun Ock, Hee-Jae Cha, Dong-Il Chung
Korean J Parasitol 2019;57(4):417-422.
Published online August 31, 2019
DOI: https://doi.org/10.3347/kjp.2019.57.4.417
From October 2015 to August 2018, tapeworm proglottids were obtained from 10 patients who were residents of Daegu and Gyeongbuk provinces and had a history of raw beef consumption. Most of them had no overseas travel experience. The gravid proglottids obtained from the 10 cases had 15-20 lateral uterine branches. A part of internal transcribed spacer 1 (ITS1) DNA of the 10 cases, amplified by polymerase chain reaction (PCR) and digested with AleI restriction enzyme, produced the same band pattern of Taenia saginata, which differentiated from T. asiatica and T. solium. Sequences of ITS1 and cytochrome c oxidase subunit 1 (cox1) showed higher homology to T. saginata than to T. asiatica and T. solium. Collectively, these 10 cases were identified as T. saginata human infections. As taeniasis is one of the important parasitic diseases in humans, it is necessary to maintain hygienic conditions during livestock farming to avoid public health concerns.

Citations

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  • Exploring bioactive molecules released during inter- and intraspecific competition: A paradigm for novel antiparasitic drug discovery and design for human use
    Pichet Ruenchit
    Current Research in Parasitology & Vector-Borne Diseases.2025; 7: 100256.     CrossRef
  • Taeniasis impacts human gut microbiome composition and function
    Wenjie Mu, Pingping Ma, Yugui Wang, Yaqi Li, Yingying Ding, Yang Zou, Lixia Pu, Qi Yan, Haoyue Kong, Xiaola Guo, Aijiang Guo, Hailong Li, Shuai Wang
    The ISME Journal.2024;[Epub]     CrossRef
  • Taenia saginata Infection Misdiagnosed as Acute Cholecystitis in a Tibetan Patient, in China
    Xiu-Min Han, Xue-Yong Zhang, Ying-Na Jian, Qing-Shan Tian
    The Korean Journal of Parasitology.2021; 59(3): 311.     CrossRef
  • 11,892 View
  • 239 Download
  • 4 Web of Science
  • Crossref

Original Article

Establishment of a Tm-shift Method for Detection of Cat-Derived Hookworms
Yeqi Fu, Yunqiu Liu, Asmaa M.I. Abuzeid, Yue Huang, Xue Zhou, Long He, Qi Zhao, Xiu Li, Jumei Liu, Rongkun Ran, Guoqing Li
Korean J Parasitol 2019;57(1):9-15.
Published online February 26, 2019
DOI: https://doi.org/10.3347/kjp.2019.57.1.9
Melting temperature shift (Tm-shift) is a new detection method that analyze the melting curve on real-time PCR thermocycler using SYBR Green I fluorescent dye. To establish a Tm-shift method for the detection of Ancylostoma ceylanicum and A. tubaeforme in cats, specific primers, with GC tail of unequal length attached to their 5 ? end, were designed based on 2 SNP loci (ITS101 and ITS296) of the internal transcribed spacer 1 (ITS1) sequences. The standard curve of Tm-shift was established using the standard plasmids of A. ceylanicum (AceP) and A. tubaeforme (AtuP). The Tm-shift method stability, sensitivity, and accuracy were tested with reference to the standard curve, and clinical fecal samples were also examined. The results demonstrated that the 2 sets of primers based on the 2 SNPs could accurately distinguish between A. ceylanicum and A. tubaeforme. The coefficient of variation (CV) of Tm-values of AceP and AtuP was 0.07% and 0.06% in ITS101 and was 0.06% and 0.08% in ITS296, respectively. The minimum detectable DNA concentration was 5.22×10-6 and 5.28×10-6 ng/μl samples of AceP and AtuP, respectively. The accuracy of Tm-shift method reached 100% based on examination of 10 hookworm DNA samples with known species. In the clinical detection of hookworm in 69 stray cat fecal sample, the Tm-shift detection results were consistent with the microscopic examination and successfully differentiated between the 2-hookworm species. In conclusion, the developed method is a rapid, sensitive and accurate technique and can provide a promising tool for clinical detection and epidemiological investigation of cat-derived hookworms.

Citations

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  • Genetic characterization of zoonotic hookworms infecting wild felids in northern India
    Thangam Venkatesan, Rasmita Panda, Anil Kumar Nehra, Hira Ram, M. Karikalan, Devendra Prasad Pateer, Rajat Garg, A. M. Pawde
    BMC Veterinary Research.2025;[Epub]     CrossRef
  • A novel A > G polymorphism in the intron 2 of TBX3 gene is significantly associated with body size in donkeys
    Gang Wang, Mei Li, Jun Zhou, Xiaoya An, Fuxia Bai, Yuan Gao, Jie Yu, Haijing Li, Chuzhao Lei, Ruihua Dang
    Gene.2021; 785: 145602.     CrossRef
  • Cutaneous Larva Migrans
    Alfonso J. Rodriguez-Morales, Natalia González-Leal, Maria Camila Montes-Montoya, Lorena Fernández-Espíndola, D. Katterine Bonilla-Aldana, José María Azeñas- Burgoa, Juan Carlos Diez de Medina, Verónica Rotela-Fisch, Melany Bermudez-Calderon, Kovy Arteaga
    Current Tropical Medicine Reports.2021; 8(3): 190.     CrossRef
  • 8,594 View
  • 101 Download
  • 4 Web of Science
  • Crossref

Brief Communications

Molecular Description of Macroorchis spinulosus (Digenea: Nanophyetidae) Based on ITS1 Sequences
Eun Jeong Won, Deok-Gyu Kim, Jaeeun Cho, Bong-Kwang Jung, Min-Jae Kim, Yong Woon Yun, Jong-Yil Chai, Dong Wook Ryang
Korean J Parasitol 2016;54(1):109-112.
Published online February 26, 2016
DOI: https://doi.org/10.3347/kjp.2016.54.1.109
We performed a molecular genetic study on the sequences of 18S ribosomal RNA (ITS1 region) gene in 4-day-old adult worms of Macroorchis spinulosus recovered in mice experimentally infected with metacercariae from crayfish in Jeollanam-do Province, Korea. The metacercariae were round, 180 μm in average diameter, encysted with 2 layers of thick walls, but the stylet on the oral sucker was not clearly seen. The adult flukes were oval shape, and 760-820 μm long and 320-450 μm wide, with anterolateral location of 2 large testes. The phylogenetic tree based on ITS1 sequences of 6 M. spinulosus samples showed their distinguished position from other trematode species in GenBank. The most closely resembled group was Paragonimus spp. which also take crayfish or crabs as the second intermediate host. The present study is the first molecular characterization of M. spinulosus and provided a basis for further phylogenetic studies to compare with other trematode fauna in Korea.

Citations

Citations to this article as recorded by  Crossref logo
  • Origins, phylogenetic relationships and host-parasite interactions of Troglotrematoidea since the cretaceous
    Konstantin S. Vainutis, Anastasia N. Voronova, Georg G. Duscher, Egor M. Shchelkanov, Mikhail Yu. Shchelkanov
    Infection, Genetics and Evolution.2022; 101: 105274.     CrossRef
  • Morphological and Molecular Characteristics of Clinostomid Metacercariae from Korea and Myanmar
    Eun Jeong Won, Yu Jeong Lee, Moon-Ju Kim, Jong-Yil Chai, Byoung-Kuk Na, Woon-Mok Sohn
    The Korean Journal of Parasitology.2020; 58(6): 635.     CrossRef
  • Metagonimus suifunensis sp. n. (Trematoda: Heterophyidae) from the Russian Southern Far East: Morphology, life cycle, and molecular data
    P.G. Shumenko, Y.V. Tatonova, V.V. Besprozvannykh
    Parasitology International.2017; 66(1): 982.     CrossRef
  • 8,599 View
  • 109 Download
  • 3 Web of Science
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Anisakis pegreffii Larvae in Sea Eels (Astroconger myriaster) from the South Sea, Republic of Korea
Jaeeun Cho, Hyemi Lim, Bong-Kwang Jung, Eun-Hee Shin, Jong-Yil Chai
Korean J Parasitol 2015;53(3):349-353.
Published online June 30, 2015
DOI: https://doi.org/10.3347/kjp.2015.53.3.349
Anisakis simplex sensu stricto (s.s.), Anisakis pegreffii, Anisakis berlandi (=A. simplex sp. C), and Anisakis typica are the 4 major species of Anisakis type I larvae. In the Republic of Korea (Korea), A. pegreffii, A. berlandi, and A. typica larvae in fish hosts has seldom been documented. In this study, molecular analysis was performed on Anisakis larvae from the sea eels (Astroconger myriaster), the major source of human anisakiasis in Korea, collected from Tongyeong City, a southern coastal area of Korea. All 20 sea eels examined were infected with Anisakis type I larvae (160 larvae; 8 per fish). Their species were analyzed using PCR-RFLP patterns and nucleotide sequences of internal transcribed spacers (ITS1, 5.8 subunit gene, and ITS2) and mitochondrial cytochrome c oxidase 2 (cox2). Most (86.8%; 112/129) of the Anisakis type I larvae were A. pegreffii, and 7.8% (10/129) were A. typica. The remaining 5.4% (7/129) was not identified. Thus, A. pegreffii is the major species of anisakid larvae in sea eels of the southern coast of Korea.

Citations

Citations to this article as recorded by  Crossref logo
  • Anisakidae and Anisakidosis: A Public Health Perspective
    Diana Nonković, Vanja Tešić, Vida Šimat, Svjetlana Karabuva, Alan Medić, Jerko Hrabar
    Pathogens.2025; 14(3): 217.     CrossRef
  • Rapid and Ultrasensitive Detection of H. aduncum via the RPA-CRISPR/Cas12a Platform
    Xiaoming Wang, Xiang Chen, Ting Xu, Xingsheng Jin, Junfang Jiang, Feng Guan
    Molecules.2024; 29(20): 4789.     CrossRef
  • Genetic analyses of Anisakis pegreffii (Nematoda: Anisakidae) from the East Asian finless porpoise Neophocaena asiaeorientalis sunameri (Cetacea: Phocoenidae) in Korean waters
    Sunmin Kim, Jong Yoon Jeon, Kyunglee Lee, Hyunjoo Lee, Han Chan Park, Kyung Eun Lee, Hang Lee, Sung Bin Lee, Sang Wha Kim, Se Chang Park, Seongjun Choe, Heejeong Youn
    Parasitology Research.2024;[Epub]     CrossRef
  • Prevalence of Anisakid Nematodes in Fish in China: A Systematic Review and Meta-Analysis
    Qing Liu, Qi Wang, Jing Jiang, Jun-Yang Ma, Xing-Quan Zhu, Qing-Long Gong
    Frontiers in Veterinary Science.2022;[Epub]     CrossRef
  • Demographic history and population genetic structure of Anisakis pegreffii in the cutlassfish Trichiurus japonicus along the coast of mainland China and Taiwan
    Fang Ding, Sui Gu, Mu-Rong Yi, Yun-Rong Yan, Wei-Kuang Wang, Kwong-Chung Tung
    Parasitology Research.2022; 121(10): 2803.     CrossRef
  • First morphological and molecular identification of third-stage larvae of Anisakis typica (Nematoda: Anisakidae) from marine fishes in Vietnamese water
    Hoang Van Hien, Bui Thi Dung, Ha Duy Ngo, Pham Ngoc Doanh
    Journal of Nematology.2021; 53(1): 1.     CrossRef
  • Comparison of risk factors between human intestinal and gastric Anisakiasis
    Kazuki Yamamoto, Osamu Takahashi, Daiki Kobayashi
    Parasitology International.2020; 75: 102024.     CrossRef
  • Genera and Species of the Anisakidae Family and Their Geographical Distribution
    Juan C. Ángeles-Hernández, Fabian R. Gómez-de Anda, Nydia E. Reyes-Rodríguez, Vicente Vega-Sánchez, Patricia B. García-Reyna, Rafael G. Campos-Montiel, Norma L. Calderón-Apodaca, Celene Salgado-Miranda, Andrea P. Zepeda-Velázquez
    Animals.2020; 10(12): 2374.     CrossRef
  • Establishment and validation of ARMS (amplification-refractory mutation system) for identification of Anisakis species collected from Korean waters
    Hyunsu Kim, Kyung-Wan Baek, Mi-Kyung Park, Kyung-Yoon Jeon, Eun-Ji Ko, Hee-Jae Cha, Mee Sun Ock
    Gene.2019; 691: 125.     CrossRef
  • Molecular Identification of Anisakis Larvae Extracted by Gastrointestinal Endoscopy from Health Check-up Patients in Korea
    Hyemi Song, Bong-Kwang Jung, Jaeeun Cho, Taehee Chang, Sun Huh, Jong-Yil Chai
    The Korean Journal of Parasitology.2019; 57(2): 207.     CrossRef
  • Anisakid Larvae from Anchovies in the South Coast of Korea
    Taehee Chang, Bong-Kwang Jung, Sooji Hong, Hyejoo Shin, Jeonggyu Lee, Laddawan Patarwut, Jong-Yil Chai
    The Korean Journal of Parasitology.2019; 57(6): 699.     CrossRef
  • Anisakiasis Causing Acute Dysentery in Malaysia
    Amirah Amir, Romano Ngui, Yee-Ling Lau, Wan Hafiz Wan Ismail, Rohela Mahmud, Kum T. Wong, Jaxinthe S. K. Ong, Yvonne A. L. Lim
    The American Journal of Tropical Medicine and Hygiene.2016; 95(2): 410.     CrossRef
  • 10,570 View
  • 119 Download
  • 13 Web of Science
  • Crossref
Case Report
A Case of Fatal Strongyloidiasis in a Patient with Chronic Lymphocytic Leukemia and Molecular Characterization of the Isolate
Eshrat Beigom Kia, Hamid Reza Rahimi, Hossein Mirhendi, Mohammad Reza Nilforoushan, Ardeshir Talebi, Farzaneh Zahabiun, Hamid Kazemzadeh, Ahmad Reza Meamar
Korean J Parasitol 2008;46(4):261-263.
Published online December 20, 2008
DOI: https://doi.org/10.3347/kjp.2008.46.4.261

Strongyloides stercoralis is a human intestinal parasite which may lead to complicated strongyloidiasis in immunocompromised. Here, a case of complicated strongyloidiasis in a patient with chronic lymphocytic leukemia is reported. Presence of numerous S. stercoralis larvae in feces and sputum confirmed the diagnosis of hyperinfection syndrome in this patient. Following recovery of filariform larvae from agar plate culture of the stool, the isolate was characterized for the ITS1 region of ribosomal DNA gene by nested-PCR and sequencing. Albendazole therapy did not have cure effects; and just at the beginning of taking ivermectin, the patient died. The most important clue to prevent such fatal consequences is early diagnosis and proper treatment.

Citations

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  • Multifaceted clinical presentations and predisposing factors of Strongyloides stercoralis and its treatment outcome: A case series
    Subhayan Das Gupta, Rohon Das Roy, Dipmala Das
    Tropical Doctor.2025; 55(4): 339.     CrossRef
  • Severe strongyloidiasis: a systematic review and meta-analysis of 339 cases
    Olga C Rojas, Alexandra M Montoya, Hiram Villanueva-Lozano, Diego Carrion-Alvarez
    Transactions of The Royal Society of Tropical Medicine and Hygiene.2023; 117(10): 682.     CrossRef
  • Fatal Disseminated Strongyloidiasis in an Immunosuppressed Patient During COVID-19 Pandemic
    Eissa Soleymani, Lotfollah Davoodi, Shadi Shayesteh Azar, Seyed Reza Mirbadiei, Fatemeh Parandin, Afshin Azimi, Azadeh Mizani, Zohreh Khorshidvand, Mahdi Fakhar
    Acta Parasitologica.2023; 68(3): 711.     CrossRef
  • Molecular characterization of human isolates of Strongyloides stercoralis and Rhabditis spp. based on mitochondrial cytochrome c oxidase subunit 1 (cox1)
    Mandana Fadaei Tehrani, Meysam Sharifdini, Farzaneh Zahabiun, Robabeh Latifi, Eshrat Beigom Kia
    BMC Infectious Diseases.2019;[Epub]     CrossRef
  • Strongyloidiasis in northern Vietnam: epidemiology, clinical characteristics and molecular diagnosis of the causal agent
    Nguyen Van De, Pham Ngoc Minh, Le Van Duyet, Santiago Mas-Coma
    Parasites & Vectors.2019;[Epub]     CrossRef
  • Effects of dexamethasone, cyclosporine and betamethasone on inflammatory cell recruitment in mice infected with Strongyloides venezuelensis
    Eleuza R Machado, Marlene T Ueta, Rosângela Maria Rodrigues, Simone G Ramos, Virgínia Vilhena, Anna Maly de Leão e Neves Eduardo, Leandro Junio Barreto dos Reis, Raphael da Silva Affonso, Lúcia Helena Faccioli
    Journal of Lung, Pulmonary & Respiratory Research.2019; 6(4): 108.     CrossRef
  • Strongyloides stercoralis hyperinfection in an unconscious diabetic patient with dermatomyositis
    Meysam Sharifdini, Aniseh Hesari, SeifAli Mahdavi, Akram Alipour, EshratBeigom Kia
    Indian Journal of Pathology and Microbiology.2018; 61(1): 109.     CrossRef
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    Tiago Mendes, Karen Minori, Marlene Ueta, Danilo Ciccone Miguel, Silmara Marques Allegretti
    Journal of Parasitology Research.2017; 2017: 1.     CrossRef
  • Case Report: Strongyloides stercoralis Hyperinfection in a Patient with Chronic Lymphocytic Leukemia
    Aimee Wilkin, Elizabeth Palavecino, Richelle Guerrero-Wooley, Ernesto Aranda-Aguirre, Wencheng Li
    The American Journal of Tropical Medicine and Hygiene.2017; 97(5): 1629.     CrossRef
  • A PCR-Based Molecular Detection of Strongyloides stercoralis in Human Stool Samples from Tabriz City, Iran
    Reza Ghasemikhah, Mohammad Tabatabaiefar, Seyed Shariatzadeh, Abbas Shahbazi, Teymour Hazratian
    Scientia Pharmaceutica.2017; 85(2): 17.     CrossRef
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    Reza Rafiei, Abdollah Rafiei, Mahmoud Rahdar, Bijan Keikhaie
    Parasite Epidemiology and Control.2016; 1(3): 229.     CrossRef
  • Strong-LAMP: A LAMP Assay for Strongyloides spp. Detection in Stool and Urine Samples. Towards the Diagnosis of Human Strongyloidiasis Starting from a Rodent Model
    Pedro Fernández-Soto, Alicia Sánchez-Hernández, Javier Gandasegui, Cristina Bajo Santos, Julio López-Abán, José María Saugar, Esperanza Rodríguez, Belén Vicente, Antonio Muro, James S McCarthy
    PLOS Neglected Tropical Diseases.2016; 10(7): e0004836.     CrossRef
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    M. Le, K. Ravin, A. Hasan, H. Clauss, D.G. Muchant, J.K. Pasko, G. Cipollina, F. Abanyie, S.P. Montgomery, M. Loy, M. Ahmed, M. Mathur, B. Chokkalingam Mani, J. Mehr, A. Kotru, C. Varma, M. Maksimak, M. Schultz, G. Obradovic, R. Alvarez, Y. Toyoda, M. Bir
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    Infection.2014; 42(6): 1039.     CrossRef
  • Severe strongyloidiasis: a systematic review of case reports
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    BMC Infectious Diseases.2013;[Epub]     CrossRef
  • Fulminant gastrointestinal hemorrhage due to Strongyloides stercoralis hyperinfection in an AIDS patient
    Valdes Roberto Bollela, Cinara Feliciano, André Costa Teixeira, Ana Carolina Ribeiro Junqueira, Marcos Antonio Rossi
    Revista da Sociedade Brasileira de Medicina Tropical.2013; 46(1): 111.     CrossRef
  • Strongyloidiasis: An Emerging Infectious Disease in China
    Xiaohong Zhou, Anthony A. James, Chunmei Wang, Juan Li, Xiaoguang Chen, Guiyun Yan, Jiabao Xu
    The American Journal of Tropical Medicine and Hygiene.2013; 88(3): 420.     CrossRef
  • Prevalence of Strongyloides stercoralis and other intestinal parasitic infections among mentally retarded residents in central institution of southern Iran
    Azar Shokri, Khojasteh Sharifi Sarasiabi, Saeed Hosseini Teshnizi, Hamid Mahmoodi
    Asian Pacific Journal of Tropical Biomedicine.2012; 2(2): 88.     CrossRef
  • 8,479 View
  • 102 Download
  • Crossref