Relevant bibliographies by topics / Falciparum

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Falciparum'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 July 2025

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Journal articles on the topic "Falciparum"

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ARICAN ÇELİK, Aslı, Rıfat TAMALI, Gülruhsar YILMAZ, Pınar KARABACAK, and Mustafa Soner ÖZCAN. "A Rare Cause of Fever in ICU; Malaria." Acta Medica Nicomedia 5, no. 3 (2022): 235–37. http://dx.doi.org/10.53446/actamednicomedia.1103400.

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Sıtma, anofel cinsi sivrisineklerin insanları sokması sonucu bulaşan paraziter bir hastalıktır. Plasmodium falciparum (P Falciparum) en ölümcül tabloya yol açan türüdür, ülkemizde nadir görülür ve genellikle yurtdışı kaynaklıdır. Yoğun bakımda yüksek ateş pek çok klinik durumda karşımıza çıksa da nadir görülen bir durum olan P. Falciparuma bağlı sıtma aklımızda bulunmalıdır Bu olgu sunumunda, yurt dışı seyahat öyküsü bulunan P. Falciparum sıtma tanısı konulan hastanın yoğun bakım takip ve tedavi süreci sunulmuştur.
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Ren, Yi. "Peroxisome Proliferator-Activator Receptorγ: A Link between Macrophage CD36 and Inflammation in Malaria Infection". PPAR Research 2012 (2012): 1–6. http://dx.doi.org/10.1155/2012/640769.

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Severe malaria infection caused byPlasmodium falciparumis a global life-threatening disease and a leading cause of death worldwide. Intensive investigations have demonstrated that macrophages play crucial roles in control of inflammatory and immune responses and clearance ofPlasmodium-falciparum-parasitized erythrocytes (PE). This paper focuses on how macrophage CD36 recognizes and internalizes PE and participates the inflammatory signaling in response toPlasmodium falciparum. In addition, recent advances in our current understanding of the biological actions of PPARγ on CD36 and malaria clear
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Cserti, Christine M., and Walter H. Dzik. "The ABO blood group system and Plasmodium falciparum malaria." Blood 110, no. 7 (2007): 2250–58. http://dx.doi.org/10.1182/blood-2007-03-077602.

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In the century since the discovery of the ABO blood groups, numerous associations between ABO groups and disease have been noted. However, the selection pressures defining the ABO distributions remain uncertain. We review published information on Plasmodium falciparum infection and ABO blood groups. DNA sequence information dates the emergence and development of the group O allele to a period of evolution before human migration out of Africa, concomitant with P falciparum's activity. The current geographic distribution of group O is also consistent with a selection pressure by P falciparum in
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Engelbrecht, Dewaldt, Pierre Marcel Durand, and Thérèsa Louise Coetzer. "On Programmed Cell Death inPlasmodium falciparum: Status Quo." Journal of Tropical Medicine 2012 (2012): 1–15. http://dx.doi.org/10.1155/2012/646534.

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Conflicting arguments and results exist regarding the occurrence and phenotype of programmed cell death (PCD) in the malaria parasitePlasmodium falciparum. Inconsistencies relate mainly to the number and type of PCD markers assessed and the different methodologies used in the studies. In this paper, we provide a comprehensive overview of the current state of knowledge and empirical evidence for PCD in the intraerythrocytic stages ofP. falciparum. We consider possible reasons for discrepancies in the data and offer suggestions towards more standardised investigation methods in this field. Furth
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Umar, Khairuddin Zainuddin, Yuri P.Utami, and Muhammad A.Y. Ardi. "Antimalarial Activity of Ethanol Extract of Sampare Leaves (Glochidion sp var. Biak) Against Plasmodium falciparum In Vitro." Indonesian Journal of Pharmaceutical Science and Technology 10, no. 1 (2023): 10. http://dx.doi.org/10.24198/ijpst.v10i1.29477.

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Malaria is one of the health problems in the world and in Indonesia. This disease is caused by theprotozoan parasite, the genus Plasmodium. Plasmodium falciparum is the most important parasiticdisease with high morbidity and mortality in the world and tropical countries such as Indonesia inparticular. This study aims to determine the activity of sampare leaf extract in inhibiting the growth ofthe FCR-3 strain of the P. falciparum parasite which causes malaria. Sampare leaves were extracted bymaceration method using 70% ethanol. Extract the results extraction were tested against P. falciparumby
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MD, Dr Tapan Biswas. "Artesunate Resistant Plasmodium Falciparum." Journal of Medical Science And clinical Research 05, no. 04 (2017): 20025–27. http://dx.doi.org/10.18535/jmscr/v5i4.48.

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Sariyanto, Iwan. "Aktivitas SGOT Dan SGPT Pada Penderita Malaria Falciparum Dan Malaria Vivax Di Puskesmas Hanura Kecamatan Teluk Pandan Kabupaten Pesawaran." Jurnal Analis Kesehatan 7, no. 1 (2018): 666. http://dx.doi.org/10.26630/jak.v7i1.913.

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<p>Penyakit Malaria bersifat endemik di daerah tropis dan subtropis. <em>Plasmodium falciparum</em> dan <em>plasmodium vivax</em> merupakan penyebab malaria terbanyak di Indonesia. <em>Plasmodium falciparum</em> menginvasi sel darah merah hingga mencapai 50%. Pembesaran hati lebih sering ditemukan dari pada pembesaran limpa. Sedangkan pada <em>plasmodium vivax </em> menginveksi retikulosit, sehingga parasitemia biasanya terbatas sekitar 2-5%,<em> </em>dapat terjadi relaps, karena maturasi hipnozoit yang tertinggal dalam hati. &l
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Maslachah, Lilik, Yoes Prijatna Dachlan, Chairul A. Nidom, and Loeki Enggar Fitr. "Experimental Models Point Mutations In Plasmodium falciparum pfatpase6 Gene Exposed to Recuring Artemisinin In Vitro." KnE Life Sciences 3, no. 6 (2017): 422. http://dx.doi.org/10.18502/kls.v3i6.1151.

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The aims of this research to prove that repeated exposure of artemisinin can cause pfatpase6 gene mutation on Plasmodium falciparum in vitro. The research methods used culture In Vitro Plasmodium falciparum of strain 2300 IC50 value determination test artemisinin, artemisinin repeated exposure test (PO1, PO2, PO3 dan PO4) dose IC50, DNA extraction, gene amplification of pfatpase6 using Polymerase Chain Reaction (PCR) technique, electrophoresis, PCR product purification, labeling DNA from PCR results, DNA precipitation of PCR product, application of product labeling on the sequencing machines,
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Wångdahl, Andreas, Katja Wyss, Dashti Saduddin, et al. "Severity of Plasmodium falciparum and Non-falciparum Malaria in Travelers and Migrants: A Nationwide Observational Study Over 2 Decades in Sweden." Journal of Infectious Diseases 220, no. 8 (2019): 1335–45. http://dx.doi.org/10.1093/infdis/jiz292.

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Abstract Background The aim was to assess factors affecting disease severity in imported P. falciparum and non-falciparum malaria. Methods We reviewed medical records from 2793/3260 (85.7%) of all episodes notified in Sweden between 1995 and 2015 and performed multivariable logistic regression. Results Severe malaria according to WHO 2015 criteria was found in P. falciparum (9.4%), P. vivax (7.7%), P. ovale (5.3%), P. malariae (3.3%), and mixed P. falciparum episodes (21.1%). Factors associated with severe P. falciparum malaria were age <5 years and >40 years, origin in nonendemic countr
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Tiwari, Aparna, and Abhinav Sinha. "Etymologia: Falciparum." Emerging Infectious Diseases 27, no. 2 (2021): 470. http://dx.doi.org/10.3201/eid2702.et2702.

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Dissertations / Theses on the topic "Falciparum"

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Buthsaraporn, Surakhaka Polrat Wilairatana. "Therapeutic response of falciparum malaria in relation to in vitro sensitivity of plasmodium falciparum /." Abstract, 2000. http://mulinet3.li.mahidol.ac.th/thesis/2543/43E-Buthsaraporn-S.pdf.

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Thiên. "Glucose metabolism in falciparum Malaria." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2004. http://dare.uva.nl/document/74040.

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Krishna, S. "Cation atpases in Plasmodium falciparum." Thesis, University of Oxford, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.293442.

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Holland, Zoe. "Plasmodium falciparum protein kinase CK2." Thesis, University of Glasgow, 2008. http://theses.gla.ac.uk/606/.

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Malaria, caused by infection with intracellular protozoan parasites of the genus Plasmodium, is responsible for 300 to 600 million clinical cases annually (Snow et al., 2005), resulting in the deaths of up to three million people every year (Breman, 2001, Breman et al., 2004). There is a clear need for further research aimed at identifying novel drug targets (Ridley, 2002). Reversible phosphorylation of proteins is a major regulatory mechanism in most cellular processes, and protein kinases are considered promising drug targets, comprising as much as 30% of all protein targets under investigat
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Patzewitz, Eva-Maria. "Glutathione metabolism of Plasmodium falciparum." Thesis, University of Glasgow, 2009. http://theses.gla.ac.uk/913/.

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Apicomplexan parasites of the genus Plasmodium are the causative agent of malaria, one of the most prevalent infectious diseases worldwide. Five different Plasmodium species can cause malaria in humans, leading to a total of approximately 500 million cases each year and of these, P. falciparum causes the most deadly form of the disease and is responsible for more than 1 million deaths annually. A major problem in the global fight against malaria is the widespread resistance of the parasites against the currently available drugs. It is of great importance to identify new drug target as well as
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Quashie, Neils Benjamin. "Purine transport in plasmodium falciparum." Thesis, Thesis restricted. Connect to e-thesis to view abstract, 2008. http://theses.gla.ac.uk/165/.

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Thesis (Ph.D.) -- University of Glasgow, 2008.<br>Ph.D. thesis submitted to the Division of Infection and Immunity, Institute of Biomedical and Life Sciences, University of Glasgow, 2008. Includes bibliographical references. Print version also available.
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Jones, Matthew L. "Erythrocyte invasion by Plasmodium falciparum." Thesis, Birmingham, Ala. : University of Alabama at Birmingham, 2009. https://www.mhsl.uab.edu/dt/2009r/jonesm.pdf.

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Vetelet, Philippe. "Paludisme grave à plasmodium falciparum." Bordeaux 2, 1988. http://www.theses.fr/1988BOR25294.

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Paul, Richard E. L. "The genetic diversity of Plasmodium falciparum." Thesis, University of Oxford, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318788.

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Hayward, Rhian Elizabeth. "The biology of Plasmodium falciparum gametocytes." Thesis, University of Oxford, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.360296.

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Books on the topic "Falciparum"

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Costanzo, Marna Schutte. Constraints and trade-offs in enzyme evolution of Plasmodium falciparum. Harvard University, 2010.

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Read, M. Tubulin in the erythrocytic stages of phasmodium falciparum. UMIST, 1995.

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Tarique, Mohammed. Drug Targets for Plasmodium Falciparum: Historic to Future Perspectives. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-19-4484-0.

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Murithi, James Muriungi. Dissecting the mechanisms of antiplasmodial resistance in Plasmodium falciparum. [publisher not identified], 2021.

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Golightly, Edmond Kwashie Odartey. Interaction between nutritional deficiencies and Plasmodium Falciparum malaria in the Gambia. Brunel University, 1988.

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Iqbal, Jamshaid. Erythrocyte membrane associated Plasmodium falciparum antigens, involvement in immunity and sequestration. Department of Immunology, the Wenner-Gren Institute, Stockholm University, 1994.

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Chu, Yen. Rheological beheaviour[sic] of erythrocyte rosettes induced by Plasmodium falciparum in flow. University of Birmingham, 1995.

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Patel, Samir. CD36-mediated clearance of Plasmodium falciparum-infected erythrocytes by rodent monocytes/macrophages. National Library of Canada, 2003.

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Scanfeld, Daniel. Exploring the Plasmodium falciparum Transcriptome Using Hypergeometric Analysis of Time Series (HATS). [publisher not identified], 2013.

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Verrall, B. Expresssion of the TATA box binding protein of plasmodium falciparum in heterologous systems. UMIST, 1997.

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Book chapters on the topic "Falciparum"

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Feldman, Charles, and Guy A. Richards. "Falciparum Malaria." In Critical Care Infectious Diseases Textbook. Springer US, 2001. http://dx.doi.org/10.1007/978-1-4615-1679-8_26.

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Keenihan, Sarah Hudson, Robert Gramzinksi, Sutanti Ratiwayanto, et al. "Plasmodium Falciparum." In Tropical Diseases. Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0059-9_7.

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Ringelmann, R., and Beate Heym. "Plasmodium falciparum." In Parasiten des Menschen. Steinkopff, 1991. http://dx.doi.org/10.1007/978-3-642-85397-5_72.

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Feldman, C., and G. A. Richards. "Falciparum Malaria." In Infectious Diseases in Critical Care. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-34406-3_24.

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Biddau, Marco, and Sylke Müller. "Carbon Metabolism ofPlasmodium falciparum." In Comprehensive Analysis of Parasite Biology: From Metabolism to Drug Discovery. Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527694082.ch16.

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Ginsburg, Hagai. "The biochemistry ofPlasmodium falciparum." In Advances in Malaria Research. John Wiley & Sons, Inc., 2016. http://dx.doi.org/10.1002/9781118493816.ch9.

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Mehlhorn, Heinz. "Plasmodium falciparum: Endothelial Receptors." In Encyclopedia of Parasitology. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-43978-4_4778.

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Mehlhorn, Heinz. "Plasmodium falciparum: Phylogenetic Origins." In Encyclopedia of Parasitology. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-43978-4_4782.

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Mehlhorn, Heinz. "Plasmodium falciparum: Endothelial Receptors." In Encyclopedia of Parasitology. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-27769-6_4778-1.

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Mehlhorn, Heinz. "Plasmodium falciparum: Phylogenetic Origins." In Encyclopedia of Parasitology. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-27769-6_4782-1.

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Conference papers on the topic "Falciparum"

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Verma, Ved Vrat, Yugandhar P. Reddy, Aditi Tomar, Chetan Kumar Sharma, and Varun Kumar Sharma. "Computational Approaches Based Evolutionary Analysis to Identify the Genetic Variation Among Kelch 13 Gene Linked to Artemisinin Resistance in Plasmodium Falciparum." In 2025 International Conference on Cognitive Computing in Engineering, Communications, Sciences and Biomedical Health Informatics (IC3ECSBHI). IEEE, 2025. https://doi.org/10.1109/ic3ecsbhi63591.2025.10991235.

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Quevedo, Viviana, and Bernabe Ortega-Tenezaca. "IF for the dataset of Plasmodium Falciparum." In MOL2NET 2019, International Conference on Multidisciplinary Sciences, 5th edition. MDPI, 2019. http://dx.doi.org/10.3390/mol2net-05-06253.

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Cai, Hong, Maribel Sanchez, Yufeng Wang, and Jianying Gu. "Putative Cell Cycle Related Genes in Plasmodium Falciparum." In 2009 International Joint Conference on Bioinformatics, Systems Biology and Intelligent Computing. IEEE, 2009. http://dx.doi.org/10.1109/ijcbs.2009.44.

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Evans, Krystal J., Dedreia Tull, Michael C. Hewitt, Malcolm J. McConville, Peter H. Seeberger, and Louis Schofield. "PURIFICATION OF THE GLYCOSYLPHOSPHATIDYLINOSITOL TOXIN OF PLASMODIUM FALCIPARUM." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.690.

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Omonuwa, Kennedy, Mangala Narasimhan, and Paul Mayo. "Acute Respiratory Distress Syndrome (ARDS) In Falciparum Malaria." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a4589.

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Neto, Paulo Schumann, Lohraine Talia Domingues, Isabela Reis Manzoli, Mariana Kely Diniz Gomes De Lima, and Diego Bezerra Soares. "PATOGENICIDADE DAS ESPÉCIES VIVAX E FALCIPARUM NO AGRAVAMENTO DA MALÁRIA." In II Congresso Brasileiro de Saúde On-line. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/1444.

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Introdução: A malária é uma doença infecciosa de grande relevância na parasitologia, causada essencialmente no cenário brasileiro pelas espécies de protozoários Plasmodium vivax e falciparum. Essa patologia pode ser definida como uma síndrome febril potencialmente grave, em que o principal mecanismo de transmissão ao homem ocorre pelo repasto sanguíneo da fêmea do mosquito Anopheles infectado. Objetivos: Devido a elevada prevalência no número de casos de malária no Brasil, essa doença é considerada uma endemia principalmente na região norte, onde estima-se uma taxa de incidência de 100.000 nov
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Yumang, Analyn N., Ericson D. Dimaunahan, Jennifer Dela Cruz, Geraldo C. Talisic, Gabriel Avelino R. Sampedro, and Maricor N. Soriano. "Real-Time Plasmodium Falciparum Parasitemia using Natural Neighbor Interpolation." In 2018 IEEE 10th International Conference on Humanoid, Nanotechnology, Information Technology,Communication and Control, Environment and Management (HNICEM). IEEE, 2018. http://dx.doi.org/10.1109/hnicem.2018.8666280.

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Paun, Rafael. "Factors Associated with Falciparum Malaria in Lembata, East Nusa Tenggara." In The 4th International Conference on Public Health. Masters Program in Public Health Universitas Sebelas Maret, 2018. http://dx.doi.org/10.26911/theicph.2018.01.61.

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Fogel, Gary B., Carla Islas, and David Hecht. "Modeling the evolution of drug resistance in Plasmodium falciparum DHFR." In 2013 IEEE Congress on Evolutionary Computation (CEC). IEEE, 2013. http://dx.doi.org/10.1109/cec.2013.6557572.

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Setianingrum, Anif Hanifa, Luh Kesuma Wardhani, A. Faisal Ridwan, and Silvia F. Nasution. "Identification of Plasmodium falciparum Stages Using Support Vector Machine Method." In 2019 7th International Conference on Cyber and IT Service Management (CITSM). IEEE, 2019. http://dx.doi.org/10.1109/citsm47753.2019.8965413.

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Reports on the topic "Falciparum"

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สืบหลินวงศ์, ธาดา, та จุฑาพันธุ์ พิณสวัสดิ์. รูปแบบของโปรตีนใน Plasmodium falciparum โดยอิเล็คโตรฟอรีซิสสองมิติ : รายงานวิจัยฉบับสมบูรณ์. จุฬาลงกรณ์มหาวิทยาลัย, 1988. https://doi.org/10.58837/chula.res.1988.10.

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โปรตีนในแต่ละเซลล์จะถูกสังเคราะห์ขึ้นอย่างรัดกุม มีการควบคุมในระดับยีน จึงมีคุณสมบัติเฉพาะตัวสำหรับแต่ละเซลล์หรือแต่ละชนิดของสัตว์และพืช ดังนั้น การศึกษารูปแบบของโปรตีนซึ่งถือเป็น gene product จึงอาจใช้เป็น marker ของเซลล์หรือสัตว์แต่ละชนิดได้ วัตถุประสงค์ของการวิจัยครั้งนี้เพื่อนำรูปแบบโปรตันซึ่งศึกษาโดยเทคนิค 2-D electrophoresis มาเป็น marker ของแต่ละสายพันธุ์บริสุทธิ์ของ P.falciparum โดยได้ศึกษารูปแบบโปรตีนของเม็ดเลือดแดงที่ติดเชื้อ P.falciparum ในตัวอย่างที่เป็น isolate และสายพันธุ์บริสุทธิ์รวม 70 ตัวอย่าง และศึกษาโปรตีนใน P. falciparum โดยใช้ [superscript 3 5]S-methionine incorporation, 2
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Rossan, Richard N. Drug Evaluation in the Plasmodium Falciparum-Aotus Model. Defense Technical Information Center, 1989. http://dx.doi.org/10.21236/ada210494.

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Rossan, Richard N. Drug Evaluation in the Plasmodium Falciparum - Aotus Model. Defense Technical Information Center, 1986. http://dx.doi.org/10.21236/ada211392.

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Rossan, Richard N. Drug Evaluation in the Plasmodium falciparum - Aotus Model. Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/ada232854.

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หาญยุทธนากร, พงชัย, та กาญจนา รังษีหิรัญรัตน์. การตรวจหาลำดับเบสของจีนไดไฮโดรไฟเลท รีดักเตส-ไทมิไดเลท ซินเทสของเชื้อมาเลเรียสายพันธุ์บริสุทธิ์ ที่มีระดับความไวต่อยาไพริเมทามีนต่างกัน ด้วยวิธีการหาลำดับเบสโดยตรง : รายงานผลการวิจัย. จุฬาลงกรณ์์มหาวิทยาลัย, 1998. https://doi.org/10.58837/chula.res.1998.31.

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ในอดีตยาไพริเมทามีน เป็นยาที่ให้ผลดีในการรักษษไข้มาลาเรียที่เกิดจาก Plasmodium falciparum โดยใช้ร่วมกับยาซัลฟาด็อกซิน แต่ในปัจจุบันยาดังกล่าวได้ลดความสำคัญในการใช้ลงเนื่องจากการแพร่กระจายของเชื้อมาลาเรียที่ดื้อต่อยาในส่วนต่าง ๆ ของโลกอย่างกว้างขวาง ไพริเมทามีนเป็นยาในกลุ่ม antifolate ที่สามารถยับยั้งการทำงานของเอนไซม์ dihydrofolate reductase-thymidylate synthase (DHFR-TS) ของเชื้อมาลาเรียซึ่งมีบทบาทสำคัญในการสังเคราะห์สารจำนวนนิวคลีโอไทด์ที่เป็นองค์ประกอบหลักของดีเอ็นเอ จากการศึกษาลำดับเบสของจีนที่มีรหัสในการสร้างเอนไซม์ DHFR-TS ของเชื้อมาลาเรียชนิด P. falciparum สายพันธุ์บริสุทธิ์ T9/94/RC17
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Wirth, Dyann F. New Strategies for Drug Discovery and Development for Plasmodium Falciparum. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada375802.

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Piper, Robert C. Parasite Lactate Dehydrogenase for Diagnosis of Plasmodium Falciparum. Phase II. Defense Technical Information Center, 1997. http://dx.doi.org/10.21236/adb230017.

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Obaldia, Nicanor, and III. Drug and Vaccine Evaluation in the Human-Aotus Plasmodium Falciparum Model. Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada405377.

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Rollwagen, Florence M., Nancy D. Pacheco, Jr Wistar, and Richard. Proliferative Responses of Mice to a Cloned Plasmodium Falciparum Sporozoite Antigen. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada205098.

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Makler, Michael T. Method for Evaluation of Drug Resistance for Plasmodium Falciparum. Phase 2. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/adb158380.

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