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1

Merrick, Catherine J. "Plasmodium falciparum." Emerging Topics in Life Sciences 1, no. 6 (2017): 517–23. http://dx.doi.org/10.1042/etls20170099.

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Plasmodium falciparum is a protozoan parasite that causes the most severe form of human malaria. Five other Plasmodium species can also infect humans — P. vivax, P. malariae, P. ovale curtisi, P. ovale wallikeri and P. knowlesi — but P. falciparum is the most prevalent Plasmodium species in the African region, where 90% of all malaria occurs, and it is this species that causes the great majority of malaria deaths. These were reported by the WHO at 438 000 in 2015 from an estimated 214 million cases; importantly, however, figures for the global burden of malaria tend to have wide margins of err
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Robson, K. J. H., and A. R. Berendt. "Plasmodium falciparum malaria." Current Opinion in Infectious Diseases 2, no. 5 (1989): 617–25. http://dx.doi.org/10.1097/00001432-198910000-00002.

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Iioka, Futoshi, and Katsuyo Tsuda. "Plasmodium falciparum malaria." Tenri Medical Bulletin 16, no. 2 (2013): 138–40. http://dx.doi.org/10.12936/tenrikiyo.16-022.

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MCCASLIN, R. IAN, ANDREAS PIKIS, and WILLIAM J. RODRIGUEZ. "Pediatric Plasmodium falciparum malaria." Pediatric Infectious Disease Journal 13, no. 8 (1994): 709–15. http://dx.doi.org/10.1097/00006454-199408000-00006.

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Kakaraparthi, Sweta, and Raghunath Prabhu. "Plasmodium Vivax Infection Impersonating Plasmodium Falciparum Malaria." Eurasian Journal of Medicine 46, no. 1 (2014): 50–52. http://dx.doi.org/10.5152/eajm.2014.09.

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MEHDI, SYED GHAZANFAR, and NAEEM NAQI. "FALCIPARUM MALARIA." Professional Medical Journal 18, no. 01 (2011): 64–68. http://dx.doi.org/10.29309/tpmj/2011.18.01.1860.

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Introduction: Quinine and quinidines remain the drugs of choice for chloroquine resistant Plasmodium falciparum malaria. In 1972, Chinese scientists discovered the antimalarial properties of a group of compounds from the qinghao plant (Artemisia annua) which have activity against all malaria causing parasites including multi-drug resistant strains of Plasmodium falciparum. Objective: To compare response to treatment between quinine and artemether in Plasmodium falciparum malaria. Design: Quasi-experimental study. Setting: Department of Medicine Pakistan Air Force Hospital Lahore. Period: 1st J
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7

R, K. Obi, C. Okangba C, C. Nwanebu F, U. Ndubuisi U, and M. Orji N. "Premunition in Plasmodium falciparum malaria." African Journal of Biotechnology 9, no. 10 (2010): 1397–401. http://dx.doi.org/10.5897/ajbx09.034.

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Arboleda Sánchez, J. A., V. M. Aguilar Urbano, F. J. García Rodríguez, and M. I. Mata Vázquez. "Malaria grave por Plasmodium falciparum." Medicina Intensiva 34, no. 8 (2010): 574. http://dx.doi.org/10.1016/j.medin.2010.01.004.

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Kreil, Anna, Christoph Wenisch, Gary Brittenham, Sornchai Looareesuwan, and Markus Peck-Radosavljevic. "Thrombopoietin in Plasmodium falciparum malaria." British Journal of Haematology 109, no. 3 (2000): 534–36. http://dx.doi.org/10.1046/j.1365-2141.2000.02096.x.

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10

Phillips, Rodney E., and Geoffrey Pasvol. "Anaemia of Plasmodium falciparum malaria." Baillière's Clinical Haematology 5, no. 2 (1992): 315–30. http://dx.doi.org/10.1016/s0950-3536(11)80022-3.

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Delmont, J., P. Brouqui, P. Poullin, and A. Bourgeade. "Harbour-acquired Plasmodium falciparum malaria." Lancet 344, no. 8918 (1994): 330–31. http://dx.doi.org/10.1016/s0140-6736(94)91367-6.

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12

Del Castillo Calderon, Jose Gabriel, and Angie Milena Cardenas Silva. "Malaria congénita por Plasmodium falciparum." Revista Chilena de Pediatría 91, no. 5 (2020): 749. http://dx.doi.org/10.32641/rchped.v91i5.1283.

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La malaria congénita (MC) es la infección por Plasmodium spp adquirida in útero o durante el parto y sus manifestaciones clínicas son inespecíficas. Puede causar enfermedad grave en la embarazada y en el recién nacido.Objetivo: describir dos casos de MC causados por Plasmodium falciparum, diagnóstico diferencial de sepsis en recién nacidos de gestantes que hayan visitado o residan en áreas endémicas para malaria.Casos Clínicos: Neonatos de sexo femenino, nacidos en área no endémica para malaria, diagnosticados con sepsis neonatal y tratados con antibióticos sin respuesta clínica. Después de la
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13

Stratton, Charles W. "Chloroquine-resistant Plasmodium falciparum malaria." Infectious Diseases Newsletter 11, no. 6 (1992): 46–47. http://dx.doi.org/10.1016/0278-2316(92)90003-v.

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14

Naik, Ramachandra S., OraLee H. Branch, Amina S. Woods, et al. "Glycosylphosphatidylinositol Anchors of Plasmodium falciparum." Journal of Experimental Medicine 192, no. 11 (2000): 1563–76. http://dx.doi.org/10.1084/jem.192.11.1563.

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Induction of proinflammatory cytokine responses by glycosylphosphatidylinositols (GPIs) of intraerythrocytic Plasmodium falciparum is believed to contribute to malaria pathogenesis. In this study, we purified the GPIs of P. falciparum to homogeneity and determined their structures by biochemical degradations and mass spectrometry. The parasite GPIs differ from those of the host in that they contain palmitic (major) and myristic (minor) acids at C-2 of inositol, predominantly C18:0 and C18:1 at sn-1 and sn-2, respectively, and do not contain additional phosphoethanolamine substitution in their
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15

Magnaval, J. F., A. Berry, R. Fabre, and S. Cassaing. "Plasmodium falciparum Chloroquine-Resistance Transporter Gene Detection in Imported Plasmodium falciparum Malaria Cases." Clinical Infectious Diseases 42, no. 12 (2006): 1806–7. http://dx.doi.org/10.1086/504434.

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Aird, William C., Laurent O. Mosnier, and Rick M. Fairhurst. "Plasmodium falciparum picks (on) EPCR." Blood 123, no. 2 (2014): 163–67. http://dx.doi.org/10.1182/blood-2013-09-521005.

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Abstract Of all the outcomes of Plasmodium falciparum infection, the coma of cerebral malaria (CM) is particularly deadly. Malariologists have long wondered how some patients develop this organ-specific syndrome. Data from two recent publications support a novel mechanism of CM pathogenesis in which infected erythrocytes (IEs) express specific virulence proteins that mediate IE binding to the endothelial protein C receptor (EPCR). Malaria-associated depletion of EPCR, with subsequent impairment of the protein C system promotes a proinflammatory, procoagulant state in brain microvessels.
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Vásquez, Ana María, and Alberto Tobón. "Pathogenic mechanisms in Plasmodium falciparum malaria." Biomédica 32, sup1 (2012): 106. http://dx.doi.org/10.7705/biomedica.v32i0.447.

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Se presentan los mecanismos patogénicos más conocidos en la infección por Plasmodium falciparum durante la fase eritrocitaria y extraeritrocitaria. La obstrucción vascular, explicada por los fenómenos de secuestro de glóbulos rojos parasitados y la formación de rosetas, mediados por diversos ligandos y receptores endoteliales, además de los procesos inflamatorios instaurados ante la presencia del parásito, son aspectos centrales en la patogenia de la malaria que permiten explicar los procesos de disfunción, daño y muerte celular en diferentes órganos.A partir de eventos como la lesión y la des
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18

Doorduijn, Jeanette K. "Halofantrine Treatment of Plasmodium falciparum Malaria." Annals of Internal Medicine 120, no. 2 (1994): 167. http://dx.doi.org/10.7326/0003-4819-120-2-199401150-00019.

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19

Kremsner, P. G., A. J. F. Luty, and W. Graninger. "Combination chemotherapy for Plasmodium falciparum malaria." Parasitology Today 13, no. 5 (1997): 167–68. http://dx.doi.org/10.1016/s0169-4758(97)01037-5.

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20

Collignon, Peter J., William T. Matthews, and Phillip F. Baron. "Rapid identification of Plasmodium falciparum malaria." Medical Journal of Australia 167, no. 10 (1997): 560. http://dx.doi.org/10.5694/j.1326-5377.1997.tb138894.x.

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21

Sermet-Gaudelus, I., V. Abadie, F. Stambouli, C. Hennequin, G. Lenoir, and D. Gendrel. "Haemophagocytic syndrome in Plasmodium falciparum malaria." Acta Paediatrica 89, no. 3 (2000): 368–69. http://dx.doi.org/10.1111/j.1651-2227.2000.tb01343.x.

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22

Kochar, D. K. "Cerebellar syndrome in Plasmodium falciparum malaria." QJM 92, no. 4 (1999): 233–34. http://dx.doi.org/10.1093/qjmed/92.4.233.

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23

Sehdev, Paul S. "Atovaquone/proguanil for plasmodium falciparum malaria." Pediatric Infectious Disease Journal 21, no. 8 (2002): 787–89. http://dx.doi.org/10.1097/00006454-200208000-00017.

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24

Murugavel, K., S. Saravanapavananthan, A. Anpalahan, and R. F. James. "Subarachnoid haemorrhage in Plasmodium falciparum malaria." Postgraduate Medical Journal 65, no. 762 (1989): 236–37. http://dx.doi.org/10.1136/pgmj.65.762.236.

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25

Kalanon, Ming, and Geoffrey I. McFadden. "Malaria, Plasmodium falciparum and its apicoplast." Biochemical Society Transactions 38, no. 3 (2010): 775–82. http://dx.doi.org/10.1042/bst0380775.

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Malaria, which is caused by species of the parasite genus Plasmodium, remains a major global health problem. A vestigial plastid homologous with the chloroplasts of plants and algae was discovered in malaria and related parasites from the phylum Apicomplexa and has radically changed our view of the evolutionary origins of these disease-causing protists. We now recognize that this large group of parasites had a photosynthetic ancestry and were converted into parasitism early in the evolution of animals. Apicomplexans have probably been parasitizing the animal kingdom for more than 500 million y
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26

Godfrey-Faussett, P., R. H. Behrens, and R. Kapoor. "Mononeuritis multiplex in Plasmodium falciparum malaria." Transactions of the Royal Society of Tropical Medicine and Hygiene 84, no. 3 (1990): 351–52. http://dx.doi.org/10.1016/0035-9203(90)90313-4.

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Bulaan, Ayuti, W. Riski Widya Mulyani, Agung Nova Mahendra, and I. Wayan Sumardika. "Plasmodium falciparum Serine Repeat Antigen 5 (PfSERA5): current vaccine candidate for Plasmodium falciparum malaria." Intisari Sains Medis 11, no. 1 (2020): 320. http://dx.doi.org/10.15562/ism.v11i1.573.

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28

M., Rukmini Ramya, and Rajya Lakshmi M. "A prospective comparative study of clinical profile and severity of plasmodium falciparum and plasmodium vivax in coastal Andhra Pradesh, India." International Journal of Advances in Medicine 5, no. 5 (2018): 1240. http://dx.doi.org/10.18203/2349-3933.ijam20183901.

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Background: Plasmodium falciparum (P. falciparum) causes vital organ dysfunction. The manifestation of severe form of falciparum malaria includes cerebral malaria, acidosis, severe anaemia, renal failure, hypotension, shock, disseminated intravascular coagulation and convulsion. Death rate used to be high. But vivax malaria is not presented in severe form and there is tendency of recurrence. Present study has been designed to compare clinical profile and severity of P. falciparum and Plasmodium vivax (P. vivax) malaria in coastal district of Andhra Pradesh.Methods: Present study is a prospecti
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29

Palmer, Carol J., John F. Lindo, Winslow I. Klaskala, et al. "Evaluation of the OptiMAL Test for Rapid Diagnosis of Plasmodium vivax and Plasmodium falciparum Malaria." Journal of Clinical Microbiology 36, no. 1 (1998): 203–6. http://dx.doi.org/10.1128/jcm.36.1.203-206.1998.

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The development of rapid and specific diagnostic tests to identify individuals infected with malaria is of paramount importance in efforts to control the severe public health impact of this disease. This study evaluated the ability of a newly developed rapid malaria diagnostic test, OptiMAL (Flow Inc., Portland, Oreg.), to detect Plasmodium vivax and Plasmodium falciparum malaria during an outbreak in Honduras. OptiMAL is a rapid (10-min) malaria detection test which utilizes a dipstick coated with monoclonal antibodies against the intracellular metabolic enzyme parasite lactate dehydrogenase
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30

Ravilala, Vinod Kumar, Shabbeer Ahmed, Murali Krishna Vanka, and Rajesh Seepana. "Comparison of clinical profile between Plasmodium vivax and Plasmodium falciparum malaria in children in tertiary care hospital." International Journal of Contemporary Pediatrics 5, no. 4 (2018): 1294. http://dx.doi.org/10.18203/2349-3291.ijcp20182477.

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Background: The high prevalence of uncomplicated malaria as seen in this study suggests the importance of timely diagnosis and effective treatment and encourages new activities to further decrease complicated malaria cases.Methods: In this study, malaria was diagnosed by conventional thick and thin peripheral smear stained with Leishman stain, examined under oil immersion. The slide was considered negative when there were no parasites in 100 HPF. Rapid diagnostic tests were based on detection of specific plasmodium antigen, LDH (optimal test) for Vivax and HRP2 for falciparum. The mode of pres
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31

Kumar Kochar, Dhanpat, and Banshi Lal Kumawat. "Cerebral malaria or Plasmodium falciparum malaria with hypoglycaemia." Lancet 347, no. 9014 (1996): 1549–50. http://dx.doi.org/10.1016/s0140-6736(96)90701-1.

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Karimov, I. Z., N. G. Los’-Yatsenko, A. S. Midikari, M. V. Gorovenko, and P. S. Arshinov. "Clinical and epidemiological features of imported malaria in the Republic of Crimea for a twenty-year period (1994-2014)." Kazan medical journal 95, no. 6 (2014): 916–20. http://dx.doi.org/10.17816/kmj2004.

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Aim. To identify the main clinical and epidemiological features of imported malaria in the Republic of Crimea for a twenty year period (1994-2014). Methods. Archival case reports, results of thin and thick blood films for malaria, a set of general clinical and biochemical laboratory parameters were assessed. Results. Over the past 20 years, 48 patients (including 47 men) aged 21 to 61 years were treated for imported malaria in the department of infectious diseases of the 7th City Clinical Hospital in Simferopol. 34 patients were diagnosed with Plasmodium falciparum malaria, 7 - with Plasmodium
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Chakrabartty, Subroto, and Saheli Misra. "Guillain Barre Syndrome complicating Plasmodium falciparum malaria." Journal of Pediatric Infectious Diseases 06, no. 02 (2015): 137–39. http://dx.doi.org/10.3233/jpi-2011-0313.

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AGOSTI, JAN M. "Plasmodium falciparum Malaria and Intravenous Quinidine Gluconate." Annals of Internal Medicine 103, no. 2 (1985): 307. http://dx.doi.org/10.7326/0003-4819-103-2-307_1.

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Maria, Musumeci, Simpore Jacques ., Barone Rita ., Angius Andrea ., Malaguarnera Lucia ., and Musumeci Salvatore . "Synchronic Macrophage Response and Plasmodium falciparum Malaria." Pakistan Journal of Biological Sciences 8, no. 7 (2005): 954–58. http://dx.doi.org/10.3923/pjbs.2005.954.958.

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Navarro, Mario Ordóñez, Maite Aizpún Sara, and Leyre Adrián Arrieta. "Manifestaciones atípicas en malaria por Plasmodium falciparum." FMC - Formación Médica Continuada en Atención Primaria 20, no. 7 (2013): 436–37. http://dx.doi.org/10.1016/s1134-2072(13)70624-8.

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Teklehaimanot, Awash. "CHLOROQUINE-RESISTANT PLASMODIUM FALCIPARUM MALARIA IN ETHIOPIA." Lancet 328, no. 8499 (1986): 127–29. http://dx.doi.org/10.1016/s0140-6736(86)91945-8.

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Yamey, Gavin. "Treating Plasmodium falciparum Malaria with Artemisinin Derivatives." PLoS Medicine 2, no. 11 (2005): e414. http://dx.doi.org/10.1371/journal.pmed.0020414.

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Del Castillo, Melissa, Ann Marie Szymanski, Ariella Slovin, Edward C. C. Wong, and Roberta L. DeBiasi. "Congenital Plasmodium falciparum Malaria in Washington, DC." American Journal of Tropical Medicine and Hygiene 96, no. 1 (2016): 167–69. http://dx.doi.org/10.4269/ajtmh.15-0630.

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Uludag Altun, Hatice, Yasemin Kurtoglu Gul, Emre Vudali, et al. "Plasmodium falciparum Malaria Case Originating from Uganda." Turkish Journal of Parasitology 37, no. 3 (2013): 229–32. http://dx.doi.org/10.5152/tpd.2013.52.

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Kizilates, Filiz, Hande Berk, Derya Seyman, Erdal Kurtoglu, and Nefise Oztoprak. "Plasmodium falciparum Malaria and Exchange Transfusion Application." Turkish Journal of Parasitology 39, no. 2 (2015): 151–54. http://dx.doi.org/10.5152/tpd.2015.3515.

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Malaguarnera, Lucia, and Salvatore Musumeci. "The immune response to Plasmodium falciparum malaria." Lancet Infectious Diseases 2, no. 8 (2002): 472–78. http://dx.doi.org/10.1016/s1473-3099(02)00344-4.

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Helbok, Raimund, Peter Lackner, and Erich Schmutzhard. "Severe Plasmodium falciparum malaria with peripheral gangrene." Lancet Infectious Diseases 8, no. 6 (2008): 400. http://dx.doi.org/10.1016/s1473-3099(08)70129-4.

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Salaria, Osman Nawazish, Salman Nawazish Salaria, Riyad Basir, and Misbahuddin Khaja. "A Case of Plasmodium Falciparum Malaria Presentation." Medicine 94, no. 34 (2015): e1415. http://dx.doi.org/10.1097/md.0000000000001415.

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Mantel, C. F., C. Klose, S. Scheurer, R. Vogel, A.-L. Wesirow, and U. Blenzie. "Plasmodium falciparum malaria acquired in Berlin, Germany." Lancet 346, no. 8970 (1995): 320–21. http://dx.doi.org/10.1016/s0140-6736(95)92212-1.

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Radloff, P. D., J. Philips, M. Nkeyi, et al. "Atovaquone and proguanil for Plasmodium falciparum malaria." Lancet 347, no. 9014 (1996): 1511–14. http://dx.doi.org/10.1016/s0140-6736(96)90671-6.

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Sanchez, R., J. Portilla, V. Boix, E. Merino, and J. M. Murcia. "Acalculous Cholecystitis Associated with Plasmodium falciparum Malaria." Clinical Infectious Diseases 31, no. 2 (2000): 622–23. http://dx.doi.org/10.1086/313944.

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Cunnington, A. J., E. M. Riley, and M. Walther. "Microvascular Dysfunction in Severe Plasmodium falciparum Malaria." Journal of Infectious Diseases 207, no. 2 (2012): 369–70. http://dx.doi.org/10.1093/infdis/jis681.

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NATHWANI, DILIP, PETER F. CURRIE, J. GRAHAM DOUGLAS, STEPHEN T. GREEN, and NORMAN C. SMITH. "Plasmodium falciparum malaria in pregnancy: a review." BJOG: An International Journal of Obstetrics and Gynaecology 99, no. 2 (1992): 118–21. http://dx.doi.org/10.1111/j.1471-0528.1992.tb14467.x.

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Iftikhar, S. A. "Indigenous Plasmodium falciparum malaria in Queens, NY." Archives of Internal Medicine 155, no. 10 (1995): 1099–101. http://dx.doi.org/10.1001/archinte.155.10.1099.

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