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Journal articles on the topic 'Immunodeficit'

Author: Grafiati
Published: 4 June 2021
Last updated: 17 February 2022

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1

Bonilla, Francisco A., and Raif S. Geha. "Are you immunodeficient?" Journal of Allergy and Clinical Immunology 116, no. 2 (August 2005): 423–25. http://dx.doi.org/10.1016/j.jaci.2005.05.026.

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2

Bondarenko, Andrey V., Sergey I. Pokhil, Marianna V. Lytvynenko, Tatyana V. Bocharova, and Vitaliy V. Gargin. "_EXPERIMENTAL IMMUNODEFICIENT STATE MODEL." Wiadomości Lekarskie 72, no. 9 (2019): 1761–64. http://dx.doi.org/10.36740/wlek201909210.

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Introduction: The recently described anaplasmosis infection is widespread but concerns to the insufficiently known group of diseases. The aim of our research is the development of uniform biological model for reproducing of artificial immunodeficient state by experimental anaplasmosis. Materials and methods: Algorithm of experimental anaplasmosis reproducing, consisted of such consecutive stages: 1) artificial forming of the immunodeficient state at nonlinear white mise (Mus musculus L.); 2) preparation of the tested biological material samples; 3) inoculation by prepared samples of the laboratory animals with the artificially formed immunodeficient state; 4) sampling from the dead or slaughtered (by the method of chloroformed anesthesia) experimental animals of sectional material (organs and targets tissues); 5) verification of aetiology by express detection of causative agents by the method of PCR in the selected samples of sectional material. Results: Biological model of experimental anaplasmosis have been created suitable for realization of both diagnostic and epidemiological, epizootic, ecobiological and other researches of different origin biological material samples, including samples of solid and liquid consistency material. Formed model realised in premature death of experimental animals in 17.4 % cases; resulted in an onset of disease clinical signs without death during the term of supervision in 43.8 % cases; coursed in the absence of the expressed symptoms of infection in 31.3 % cases. Conclusions: Developed biological model of experimental anaplasmosis consists in that as laboratory animals with the increased sensitiveness to the infection and accumulation of causative agent are used white nonlinear mice with the artificially formed immunodeficient state.
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3

Brown, Karen L., Karen Stewart, Moira E. Bruce, and Hugh Fraser. "Scrapie in Immunodeficient mice." Biochemical Society Transactions 25, no. 2 (May 1, 1997): 173S. http://dx.doi.org/10.1042/bst025173s.

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4

Le Bras, Alexandra. "A new immunodeficient pig model." Lab Animal 48, no. 7 (June 19, 2019): 198. http://dx.doi.org/10.1038/s41684-019-0339-1.

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5

JAVIER, LAZO, ANTONIO CARLOS OLIVEIRA MENESES, ADEMIR ROCHA, MARCELO SIMÃO FERREIRA, JAIME OLAVO MARQUEZ, EDMUNDO CHAPADEIRO, and EDILSON REIS LOPES. "Chagasic meningoencephalitis in the immunodeficient." Arquivos de Neuro-Psiquiatria 56, no. 1 (March 1998): 93–97. http://dx.doi.org/10.1590/s0004-282x1998000100015.

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Based on their own experience and on the literature, the authors compare the brain pathology due to HIV+ associated Trypanosoma cruzi reactived infection to that described for the natural history of the Chagas' disease (CD). The peculiar focal necrotizing chagasic meningoencephalitis (MECNF) which appears only in immunedeficient chagasics, especially when the deficiency is due HIV is a safe criterion for reactivation of CD. MECNF morphologic findings are unlike to those found either for some cases of acute phase CD or for chronic nervous form of CD.
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6

Leonard, Arnold S., Michael W. Mulholland, and Alexandra H. Filipovich. "Surgery of the Immunodeficient Child." Surgical Clinics of North America 65, no. 6 (December 1985): 1505–25. http://dx.doi.org/10.1016/s0039-6109(16)43784-9.

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7

Boshoff, C., and R. Weiss. "Cancer processes in immunodeficient populations." European Journal of Cancer 37, no. 10 (July 2001): 1202–8. http://dx.doi.org/10.1016/s0959-8049(01)00114-9.

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8

Belizario, Jose E. "Immunodeficient Mouse Models: An Overview." Open Immunology Journal 2, no. 1 (August 19, 2009): 79–85. http://dx.doi.org/10.2174/1874226200902010079.

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9

Kaplan, Jonathan. "Opportunistic Infections in Immunodeficient Populations." Emerging Infectious Diseases 4, no. 3 (September 1998): 421–22. http://dx.doi.org/10.3201/eid0403.980321.

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10

Castanet, J., F. Monpoux, R. Mariani, J. P. Ortonne, and J. Ph Lacour. "Demodicidosis in an Immunodeficient Child." Pediatric Dermatology 14, no. 3 (May 1997): 219–20. http://dx.doi.org/10.1111/j.1525-1470.1997.tb00242.x.

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11

Kim, Yoon-Young, Jin-Soo Kim, Jeong-Hwan Che, Seung-Yup Ku, Byeong-Cheol Kang, and Jun-Won Yun. "Comparison of Genetically Engineered Immunodeficient Animal Models for Nonclinical Testing of Stem Cell Therapies." Pharmaceutics 13, no. 2 (January 20, 2021): 130. http://dx.doi.org/10.3390/pharmaceutics13020130.

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For the recovery or replacement of dysfunctional cells and tissue—the goal of stem cell research—successful engraftment of transplanted cells and tissues are essential events. The event is largely dependent on the immune rejection of the recipient; therefore, the immunogenic evaluation of candidate cells or tissues in immunodeficient animals is important. Understanding the immunodeficient system can provide insights into the generation and use of immunodeficient animal models, presenting a unique system to explore the capabilities of the innate immune system. In this review, we summarize various immunodeficient animal model systems with different target genes as valuable tools for biomedical research. There have been numerous immunodeficient models developed by different gene defects, resulting in many different features in phenotype. More important, mice, rats, and other large animals exhibit very different immunological and physiological features in tissue and organs, including genetic background and a representation of human disease conditions. Therefore, the findings from this review may guide researchers to select the most appropriate immunodeficient strain, target gene, and animal species based on the research type, mutant gene effects, and similarity to human immunological features for stem cell research.
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12

VINARSKAYA, H. I., N. A. NIKONOVA, and A. L. SMOLYA. "THE IMMUNODEFICITS: TIME OF INFLUENCE AND ECOLOGICAL SITUATION." Epidemiology 7, Supplement (July 1996): S55. http://dx.doi.org/10.1097/00001648-199607001-00148.

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13

Clark, David A., Christine Quarrington, Daljeet Banwatt, Justin Manuel, and Gabrielle Fulop. "Spontaneous Abortion in Immunodeficient SCID Mice." American Journal of Reproductive Immunology 32, no. 1 (August 1994): 15–25. http://dx.doi.org/10.1111/j.1600-0897.1994.tb00874.x.

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14

Otrok, T. "Colonic “histoplasmoma” in an immunodeficient patient." American Journal of Gastroenterology 95, no. 9 (September 2000): 2593. http://dx.doi.org/10.1016/s0002-9270(00)01779-2.

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15

Pérez-López, Israel, José David Herrera-García, and Ricardo Ruiz-Villaverde. "Palmar hyperkeratosis in an immunodeficient patient." Medicina Clínica (English Edition) 155, no. 6 (September 2020): 279. http://dx.doi.org/10.1016/j.medcle.2019.07.015.

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16

Woodland, David L. "Immunity to Viruses in Immunodeficient Hosts." Viral Immunology 28, no. 5 (June 2015): 247. http://dx.doi.org/10.1089/vim.2015.1506.

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17

Gawronska-Kozak, Barbara, Marek Bogacki, Jong-Seop Rim, W. Todd Monroe, and Jessica A. Manuel. "Scarless skin repair in immunodeficient mice." Wound Repair and Regeneration 14, no. 3 (June 28, 2006): 265–76. http://dx.doi.org/10.1111/j.1743-6109.2006.00121.x.

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18

Franks, J. J., and J. R. Kambam. "Perioperative care of the immunodeficient patient." Current Opinion in Anaesthesiology 2, no. 3 (June 1989): 353–56. http://dx.doi.org/10.1097/00001503-198906000-00019.

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19

Moritz, T. "Immunodeficient animals: Models for cancer research." European Journal of Cancer 33, no. 2 (February 1997): 316–17. http://dx.doi.org/10.1016/s0959-8049(96)00468-6.

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20

Businoo, L., A. Cantani, E. Galli, A. Solano, S. O. Smelli, and F. Aiuti. "INTRAVENOUS GAMMAGLOBULIN THERAPY IN IMMUNODEFICIENT CHILDREN." Pediatric Research 19, no. 10 (October 1985): 1118. http://dx.doi.org/10.1203/00006450-198510000-00278.

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21

Budzynski, W., and C. Radzikowski. "Cytotoxic Cs in Immunodeficient Athymic Mice." Immunopharmacology and Immunotoxicology 16, no. 3 (January 1994): 319–46. http://dx.doi.org/10.3109/08923979409007097.

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22

Macera, Lisa, Daniele Focosi, Maria Linda Vatteroni, Aldo Manzin, Guido Antonelli, Mauro Pistello, and Fabrizio Maggi. "Cyclovirus Vietnam DNA in immunodeficient patients." Journal of Clinical Virology 81 (August 2016): 12–15. http://dx.doi.org/10.1016/j.jcv.2016.05.011.

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23

Al-Herz, Waleed, and Arti Nanda. "Skin Manifestations in Primary Immunodeficient Children." Pediatric Dermatology 28, no. 5 (March 31, 2011): 494–501. http://dx.doi.org/10.1111/j.1525-1470.2011.01409.x.

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24

Otrok, T., S. Tabriz, S. Krishnan, and S. Chokhavatia. "Colonic "histoplasmoma" in an immunodeficient patient." American Journal of Gastroenterology 95, no. 9 (September 2000): 2593. http://dx.doi.org/10.1111/j.1572-0241.2000.02987.x.

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25

Berlinger, Norman T. "SINUSITIS IN IMMUNODEFICIENT AND IMMUNOSUPPRESSED PATIENTS." Laryngoscope 95, no. 1 (January 1985): 29???33. http://dx.doi.org/10.1288/00005537-198501000-00009.

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26

Stein, C. Michael. "Immunodeficient states and associated rheumatic manifestations." Current Opinion in Rheumatology 8, no. 1 (January 1996): 52–56. http://dx.doi.org/10.1097/00002281-199601000-00010.

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27

Imada, Kazunori. "Immunodeficient Mouse Models of Lymphoid Tumors." International Journal of Hematology 77, no. 4 (May 2003): 336–41. http://dx.doi.org/10.1007/bf02982640.

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28

Walters, M. D. S., J. E. Deanfield, P. J. Robinson, and D. J. Matthew. "Obstructive endocarditis in an immunodeficient infant." European Journal of Pediatrics 145, no. 6 (December 1986): 553–54. http://dx.doi.org/10.1007/bf02429063.

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29

Caroleo, M. Cristina, Daniela Frasca, Giuseppe Nisticó, and Gino Doria. "Melatonin as immunompdulator in immunodeficient mice." Immunopharmacology 23, no. 2 (March 1992): 81–89. http://dx.doi.org/10.1016/0162-3109(92)90031-7.

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30

Salkowski, Cindy A., and Edward Balish. "Susceptibility of congenitally immunodeficient mice to a nonencapsulated strain of Cryptococcus neoformans." Canadian Journal of Microbiology 37, no. 11 (November 1, 1991): 834–39. http://dx.doi.org/10.1139/m91-144.

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The susceptibility of congenitally immunodeficient mice to a nonencapsulated strain of Cryptococcus neoformans (strain M7) was evaluated. Gnotobiotic mice with defined congenital defects in innate immunity (beige) or cell-mediated immunity (athymic) or with combined defects in innate and cellular immunity (beige athymic) were i.v. challenged with C. neoformans M7. The nonencapsulated strain of C. neoformans produced a persistant low-grade infection in the brains of all immunodeficient and immunocompetent mice used in this study. Immunocompetent mice (nu/+;bg/+) and immunodeficient bg/bg mice readily cleared nonencapsulated cryptococci from their kidneys, liver, lungs, and spleen. In contrast to nu/+ mice, nu/nu mice had a reduced capacity to clear nonencapsulated cryptococci from their kidneys and liver after i.v. challenge. Both bg/bg–nu/nu and bg/bg–nu/+ mice developed a low-grade infection in their kidneys, liver, lungs, and spleen, which was maintained throughout the 21-day study. Persistent infections were not due to reversion to an encapsulated state. These data indicate that a capsule may not always be necessary for C. neoformans to survive, in vivo, in tissues of immunodeficient and immunocompetent mice. Key words: Cryptococcus neoformans, capsule, immunodeficient mice.
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31

Falcone, Valeria, Marcus Panning, Brigitte Strahm, Thomas Vraetz, Sibylle Bierbaum, Dieter Neumann-Haefelin, and Daniela Huzly. "Prolonged KI Polyomavirus Infection in Immunodeficient Child." Emerging Infectious Diseases 18, no. 4 (April 2012): 706–8. http://dx.doi.org/10.3201/eid1804.111588.

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32

Rajan, T. V., J. M. Moore, and L. D. Shultz. "Immunodeficient mice as hosts for hemoparasitic infections." Parasitology Today 12, no. 12 (December 1996): 479–85. http://dx.doi.org/10.1016/s0169-4758(96)10066-1.

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33

Sura, Piotr, and Zbigniew Srebro. "Cerebral Pathology in Immunodeficient Gnotobiotic Laboratory Mice." Folia Biologica 53, no. 3 (October 1, 2005): 205–8. http://dx.doi.org/10.3409/173491605775142738.

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34

Soliman, M., E. Kaplan, F. Straus, M. E. Fisfalen, Y. Hidaka, V. Guimaraes, and L. J. DeGroot. "Graves' disease in severe combined immunodeficient mice." Journal of Clinical Endocrinology & Metabolism 80, no. 10 (October 1995): 2848–55. http://dx.doi.org/10.1210/jcem.80.10.7559863.

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35

Barbera, J. R., J. A. Capdevila, and A. M. Planes. "Shewanella putrefaciens bacteremia in an immunodeficient patient." Clinical Microbiology Newsletter 18, no. 7 (April 1996): 53–55. http://dx.doi.org/10.1016/s0196-4399(96)80012-2.

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36

Weber, R., and R. T. Bryan. "Microsporidial Infections in Immunodeficient and Immunocompetent Patients." Clinical Infectious Diseases 19, no. 3 (September 1, 1994): 517–21. http://dx.doi.org/10.1093/clinids/19.3.517.

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37

Campisi, Paolo, Linda Vong, Jonathan M. Sgro, Nikolaus Wolter, Bo Ngan, and Jacob Friedberg. "Transcervical thymic biopsy in the immunodeficient child." LymphoSign Journal 6, no. 4 (December 1, 2019): 141–47. http://dx.doi.org/10.14785/lymphosign-2019-0014.

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Objective: The objectives of this study are to present a case series of immunodeficient children who underwent a transcervical thymic biopsy and to describe the transcervical approach to the thymus gland. Design: Case series. Setting: Pediatric otolaryngology practice in an academic setting. Patients: Consecutive sample of immunodeficient children (≤18 years old) who underwent thymic biopsies from 1996 to 2019 for the purpose of confirming or excluding profound T cell immunodeficiency. Intervention: Diagnostic transcervical thymic biopsy. Results: A total of 14 patients with atypical combined immunodeficiency underwent the procedure during the study period, with minimal post-operative complication. The thymus was found to be abnormal histologically in 9 children and normal in another 5 patients. In all cases, thymus morphology helped define the extent of the immunodeficiency, resulting in either supporting a decision to perform a bone marrow transplant (8 patients) or avoid this high risk procedure (3 patients). Conclusion: Thymus biopsy is helpful in the characterization of childhood immunodeficiency and provides critical information that affects the medical management. The transcervical approach to the thymus is feasible in children and can be accomplished with minimal morbidity. Statement of novelty: Biopsies of the thymus have assisted in the characterization of new entities of primary immunodeficiency.
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38

Shukhtin, VV, AI Hozhenko, and AP Levyts'kyĭ. "Pathogenesis of skin injury in immunodeficient rats." Fiziolohichnyĭ zhurnal 59, no. 4 (August 15, 2013): 63–66. http://dx.doi.org/10.15407/fz59.04.063.

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39

Soliman, M. "Graves' disease in severe combined immunodeficient mice." Journal of Clinical Endocrinology & Metabolism 80, no. 10 (October 1, 1995): 2848–55. http://dx.doi.org/10.1210/jc.80.10.2848.

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40

Dorval, Jean-Claude. "Darier-White Disease: A Multifaceted Immunodeficient State?" Archives of Dermatology 121, no. 2 (February 1, 1985): 170. http://dx.doi.org/10.1001/archderm.1985.01660020028008.

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41

Dorval, J. C. "Darier-White disease: a multifaceted immunodeficient state?" Archives of Dermatology 121, no. 2 (February 1, 1985): 170a—170. http://dx.doi.org/10.1001/archderm.121.2.170a.

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42

Davis, J. J., and M. B. Heyman. "Cryptosporidiosis and Sinusitis in an Immunodeficient Adolescent." Journal of Infectious Diseases 158, no. 3 (September 1, 1988): 649. http://dx.doi.org/10.1093/infdis/158.3.649.

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43

Song, Kyle R., Michael S. Wong, and Cecilia Yeung. "Primary Cutaneous Zygomycosis in an Immunodeficient Infant." Annals of Plastic Surgery 60, no. 4 (April 2008): 433–36. http://dx.doi.org/10.1097/sap.0b013e3181238df2.

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44

Healy, Fiona M., and Samuel B. Goldfarb. "PULMONARY ALVEOLAR MICROLITHIASIS IN AN IMMUNODEFICIENT PATIENT." Chest 136, no. 4 (October 2009): 17S. http://dx.doi.org/10.1378/chest.136.4_meetingabstracts.17s-d.

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45

Campbell, N. J., J. Longley, A. Pascalis, J. Bennett, M. Remer, R. Stone, D. Muller, et al. "Immunotherapy in the immunodeficient: A treatment paradox?" Annals of Oncology 29 (October 2018): viii429. http://dx.doi.org/10.1093/annonc/mdy288.082.

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46

Mills, Gordon C., and John S. Mills. "Urinary excretion of methylthioadenosine in immunodeficient children." Clinica Chimica Acta 147, no. 1 (March 1985): 15–23. http://dx.doi.org/10.1016/0009-8981(85)90005-1.

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47

Moriya, Osamu, and Yoichi Ichikawa. "J-chain-positive cells in immunodeficient chickens." Developmental & Comparative Immunology 17, no. 2 (March 1993): 179–84. http://dx.doi.org/10.1016/0145-305x(93)90027-n.

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48

Bernatowska, Ewa, Bożena Mikołuć, Antoni Krzeski, Barbara Piątosa, and Iwona Gromek. "Chronic rhinosinusitis in primary antibody immunodeficient patients." International Journal of Pediatric Otorhinolaryngology 70, no. 9 (September 2006): 1587–92. http://dx.doi.org/10.1016/j.ijporl.2006.04.013.

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49

Al-Herz, W. "Mortality Among Primary Immunodeficient Patients in Kuwait." Journal of Allergy and Clinical Immunology 125, no. 2 (February 2010): AB75. http://dx.doi.org/10.1016/j.jaci.2009.12.296.

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50

Lombar, A. V., M. Segovia, C. M. Carranza, M. L. Chessari, A. I. Sanchez, and A. M. Assetta. "Parvovirus B 19 infection in immunodeficient patient." International Journal of Infectious Diseases 14 (March 2010): e405. http://dx.doi.org/10.1016/j.ijid.2010.02.520.

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