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Books on the topic 'IIV infections'

Author: Grafiati

Published: 30 June 2021

Last updated: 14 February 2022

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1

International, Workshop on Campylobacter Infections (3rd 1985 Ottawa Ont ). Campylobacter III: Proceedings of the Third International Workshop on Campylobacter Infections, Ottawa, 7-10 July 1985. London: Public Health Laboratory Service, 1985.

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2

Adhikari, Rameshwar, and Santosh Thapa, eds. Infectious Diseases and Nanomedicine III. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-7572-8.

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3

National AIDS Control Programme (India). Phase--III. Targeted interventions under NACP III: Operational guidelines. New Delhi: National AIDS Control Organization, Ministry of Health & Family Welfare, Govt. of India, 2007.

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4

National AIDS Co-ordinating Agency (Botswana), ed. Botswana AIDS impact survey III: Statistical report. Gaborone: Central Statistics Office, 2009.

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5

Pollard, Andrew J., and Adam Finn, eds. Hot Topics in Infection and Immunity in Children III. Boston, MA: Springer US, 2006. http://dx.doi.org/10.1007/0-387-33026-7.

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6

National AIDS Control Programme (Tanzania). Third health sector HIV and AIDS strategic plan: (HSHSP-III) 2013-2017. Dar es Salaam: Ministry of Health and Social Welfare, National AIDS Control Programme, 2014.

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7

(India), Taylor Nelson Sofres Mode. Behavioural surveillance survey in Andhra Pradesh (WAVE III): Summary report. [New Delhi]: Resource Centre for Sexual Health and HIV/AIDS, 2007.

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8

Social, and Rural Research Institute (New Delhi India). Behavioural surveillance survey in West Bengal: WAVE III : summary report. Kolkata: West Bengal State AIDS Prevention & Control Society, 2004.

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9

Runck, Bette. Coping with AIDS: Psychological and social considerations in helping people with HTLV-III infection. Atlanta, Ga: U.S. Dept. of Health and Human Services, Public Health Service, 1986.

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10

St, Mary's Hospital (London England). AIDS and HTLV III: The St Mary's control of infection pack : district control of infection policies devised and implemented by St Mary's Hospital, Praed St, London W2. London: Paddington and North Kensington Health Authority and North West Thames Regional Health Authority, 1986.

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11

1934-, Bellanti Joseph A., ed. Neonatal hematology and immunology III: Proceedings of the Third Neonatal Hematology and Immunology Symposium, held in Washington, D.C., September 29-October 1, 1996. Amsterdam: Elsevier Science, 1997.

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12

Miller, Benjamin L. Frontiers in biological detection: From nanosensors to systems III : 22-23 January 2011, San Francisco, California, United States. Edited by SPIE (Society). Bellingham, Wash: SPIE, 2011.

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13

Kislenko, Viktor. Microbiology. Practicum. ru: INFRA-M Academic Publishing LLC., 2019. http://dx.doi.org/10.12737/1016621.

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The tutorial consists of two sections. Section I "General Microbiology" contains information about the rules of work in bacteriological laboratories, includes a description of the main microbiological, genetic and immunological methods of research. Section II "Infectious agents" lists the main properties of pathogens, methods of their identification and differentiation. Meets the requirements of the Federal state educational standards of higher education of the last generation. For students of higher educational institutions studying in the direction of training 36.03.01 "Veterinary and sanitary examination".

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14

Pearson, A. D., H. Lior, and M. B. Skirrow. Campylobacter III. Mosby-Year Book, 1986.

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15

Wilson, John W., and Lynn L. Estes. Nontuberculosis Mycobacterial Infections. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780199797783.003.0125.

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•Group I (photochromogens): Produces pigment in light: Mycobacterium kansasii, M marinum, M simiae•Group II (scotochromogens): Produces pigment in dark: M scrofulaceum, M szulgai, M xenopi, M gordonae•Group III (nonphotochromogens): No pigment: M avium-intracellulare complex (MAC), M haemophilum, M ulcerans, M malmoense, M terrae...

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16

(Editor), Naomi P. O'Grady, and Didier Pittet (Editor), eds. Catheter-Related Infections In The Critically III (Perspectives on Critical Care Infectious Diseases). Springer, 2004.

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17

Apic. Apic Infection Control Iii. Kendall/Hunt Publishing Company, 1988.

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18

DeAugustinas, M., and A. Kiely. Periocular Infections. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199976805.003.0015.

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Periocular Infections occur when there is inflammation of the conjunctiva. Uncomplicated viral infections can usually be managed with careful hand hygiene and lubrication of the eye with artificial tears. More severe infections are notable for purulent discharge, membrane formation, and scarring, and can lead to corneal change. For suspected bacterial conjunctivitis, empiric therapy begins with broad spectrum antibiotic eye drops or ointment, which are supplemented with oral antibiotics in cases associated with pharyngitis and in children with H. influenzae infection. For gonococcal conjunctivitis, systemic ceftriaxone is recommended for both adults and children (including neonates) due to the increasing prevalence of penicillin-resistant N. gonorrhoeae. If the cornea is not involved and the patient is extremely reliable, next day referral to an ophthalmologist in addition to management with IM ceftriaxone is sufficient. Otherwise, admission for IV therapy is advised. Copious, repeated irrigation is also advised to remove inflammatory mediators and debris that can contribute to corneal melting.

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19

The Pediatric Spine III: Cysts, Tumors, and Infections. Springer, 2013.

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20

Garrard, Christopher. Ciprofloxacin i.v.: Defining Its Role in Serious Infections. Springer, 1995.

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21

Choux, Maurice, Concezio Di Rocco, and Anthony J. Raimondi. The Pediatric Spine III: Cysts, Tumors, and Infections. Springer, 2011.

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22

Garrard, C. Ciprofloxacin I.V.: Defining Its Role in Serious Infections. Springer-Verlag Telos, 2000.

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23

(Editor), Andrew J. Pollard, and Adam Finn (Editor), eds. Hot Topics in Infection and Immunity in Children III (Advances in Experimental Medicine and Biology). Springer, 2006.

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24

COLOR ATLAS OF INFECTIOUS DISEASE (VOLUME II OF III). Clinical Communications, Inc, 1995.

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25

Finn, Adam, and Andrew J. Pollard. Hot Topics in Infection and Immunity in Children III. Springer, 2010.

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26

St. Mary's Hospital (London, England), Paddington and North Kensington Health Authority., and North West Thames Regional Health Authority., eds. Aids and HTLV III: The St. Mary's control of infection pack. London: Paddington and North Kensington Health Authority and North West Thames Regional Health Authority, 1986.

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27

St. Mary's Hospital (Praed Street), ed. AIDS and HTLV III: The St. Mary's control of infection pack. London: Paddington and North Kensington Health Authority and North West Thames Regional Health Authority, 1986.

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28

C, Garrard, ed. Ciprofloxacin i.v.: Defining its role in serious infections : international symposium, Salzburg, September 1993. Berlin: Springer-Verlag, 1994.

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29

Grais, Rebecca F. Research in crises: overcoming obstacles and lessons for the future. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198789833.003.0003.

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At present, there is the highest number of displaced persons since World War II. Add to that the approximately one billion people living in so-designated fragile states, as well as multiple large-scale humanitarian crises. These vulnerable populations are subject direct and indirect health effects. Unfortunately, delivering effective interventions to them is fraught with difficulty, and the evidence base is weak. The chapter examines the conditions that give rise to acute and prevalent health risks among vulnerable populations, and the present challenges to research. These issues are particularly pertinent to inform our understanding of the ecology of infectious disease. Research contributions are also essential to address infectious diseases and to weigh the relative benefits and risks of different control options. Effective research in crises provides critical information for our understanding of infections among the most vulnerable.

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30

Jacquet, Gabrielle. Deep Space Infections of the Head and Neck. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199976805.003.0014.

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Deep space infections occur around the airway, including the epiglottis, the parotid gland, and the retropharyngeal spaces (retropharyngeal abscesses [RPA]) and parapharyngeal spaces. These infections can extend into the airway and mediastinum, and their extent can be difficult to appreciate without imaging. In adults, deep space infections most commonly result from trauma, irradiation, surgical procedures, and human or animal bites. In children, they more commonly result from cervical adenitis and thyroiditis caused by bacteria or viruses. RPA commonly presents with sore throat, fever, torticollis, dysphagia, neck pain, muffled “hot potato” voice, cervical lymphadenopathy, and respiratory distress. Epiglottitis symptoms classically include the triad of drooling, dysphagia, and distress but may include inspiratory stridor. Parotitis is recognized by a sudden firm, erythematous swelling of the preauricular and postauricular areas. Immediate airway management and otolaryngology consultation are required. Most patients will require transoral or transcervical incision and drainage in addition to IV fluid resuscitation and close observation.

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31

Barsoum, Rashad S. Schistosomiasis. Edited by Vivekanand Jha. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0194_update_001.

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The urinary system is the primary target of Schistosoma haematobium infection, which leads to granuloma formation in the lower urinary tract that heals with fibrosis and calcification. While the early lesions may be associated with distressing acute or subacute symptoms, it is the late lesions that constitute the main clinical impact of schistosomiasis. The latter include chronic cystitis, ureteric fibrosis, ureterovesical obstruction or reflux which may lead to chronic pyelonephritis. Secondary bacterial infection and bladder cancer are the main secondary sequelae of urinary schistosomiasis.The kidneys are also a secondary target of S. mansoni infection, attributed to the systemic immune response to the parasite. Specific immune complexes are responsible for early, often asymptomatic, possibly reversible, mesangioproliferative lesions which are categorized as ‘class I’. Subsequent classes (II–VI) display different histopathology, more serious clinical disease, and confounding pathogenic factors. Class II lesions are encountered in patients with concomitant salmonellosis; they are typically exudative and associated with acute-onset nephrotic syndrome. Classes III (mesangiocapillary glomerulonephritis) and IV (focal segmental sclerosis) are progressive forms of glomerular disease associated with significant hepatic pathology. They are usually associated with immunoglobulin A deposits which seem to have a significant pathogenic role. Class V (amyloidosis) occurs with long-standing active infection with either S. haematobium or S. mansoni. Class VI is seen in patients with concomitant HCV infection, where the pathology is a mix of schistosomal and cryoglobulinaemic lesions, as well as amyloidosis which seems to be accelerated by the confounded pathogenesis.Early schistosomal lesions, particularly those of the lower urinary tract, respond to antiparasitic treatment. Late urological lesions may need surgery or endoscopic interventions. As a rule, glomerular lesions do not respond to treatment with the exception of class II where dual antiparasitic and antibiotic therapy is usually curative. Patients with end-stage kidney disease may constitute specific, yet not insurmountable technical and logistic problems in dialysis or transplantation. Recurrence after transplantation is rare.

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32

Adhikari, Rameshwar, and Santosh Thapa. Infectious Diseases and Nanomedicine III: Second International Conference , Dec. 15-18, 2015, Kathmandu, Nepal. Springer, 2018.

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33

Adhikari, Rameshwar, and Santosh Thapa. Infectious Diseases and Nanomedicine III: Second International Conference , Dec. 15-18, 2015, Kathmandu, Nepal. Springer, 2018.

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34

Baydoun, Hasan E., Bachar Hamade, and Jamil D. Bayram. Septic Arthritis. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199976805.003.0046.

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Septic arthritis is an infectious inflammation of a joint. It usually presents as acute, progressive pain that increases with motion and eventually leads to the inability to bear weight. The most common presenting features include joint pain, swelling, and fever. Pediatric cases are often associated with bacteremia. Gonococcal arthritis is migratory and associated with dermatitis and tenosynovitis. Optimal positioning of the joint to avoid future contractures is essential, and joint aspiration should be done as soon as possible. IV antibiotics should be given only after aspiration unless the patient is septic, in which case antibiotics should not be delayed. Orthopedic consultation is mandatory in cases of septic arthritis. In documented gonococcal arthritis with no suspicion for other concomitant infection, nonsurgical treatment may be considered if there is complete symptom resolution with IV antibiotics and joint aspiration.

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35

National Institute of Mental Health (U.S.) Office of Scientific Information, ed. Coping with AIDS: Psychological and social considerations in helping people with HTLV-III infection. Rockville, Md: U.S. Dept. of Health and Human Services, Public Health Service, Alcohol, Drug Abuse, and Mental Health Administration, National Institute of Mental Health, Office of Scientific Information, 1986.

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36

AIDS, Indonesia Komisi Penanggulangan, ed. Strategi nasional penanggulangan HIV dan AIDS, 2007-2010: Lampiran surat keputusan Menteri Koordinator Bidang Kesejahteraan Rakyat/Ketua Komisi Penanggulangan AIDS Nasional nomor 07/Kep/Menko/Kesra/III/2007. [Jakarta]: Komisi Penanggulangan AIDS Nasional, 2007.

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37

Roche, Benjamin, Hélène Broutin, and Frédéric Simard. Afterword II Fundamental knowledge in the evolutionary ecology of infectious diseases. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198789833.003.0022.

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In Part II, the main academic knowledge gathered to date on the ecology and evolution of infectious diseases with relevance for infectious diseases control in low-income countries has been reviewed. We have seen that many pathogens affecting human populations rely strongly on environmental determinants, such as climate, water, abiotic characteristics and inter-specific relationships, among other factors. This is especially important for low-income countries that are mostly located in tropical areas and, therefore, are exposed to high variability in terms of climatic conditions in environments ranging from the deep evergreen equatorial forests to arid deserts....

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38

Directrices: Quimioterapia preventiva para controlar las geohelmintiasis en grupos de población en riesgo. Organización Panamericana de la Salud, 2018. http://dx.doi.org/10.37774/9789275319949.

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La Organización Mundial de la Salud (OMS) estima que las principales geohelmintiasis —por lombriz intestinal (Ascaris lumbricoides), por tricocéfalo (Trichuris trichiura) y por uncinarias (Ancylostoma duodenale y americanus de Necator)— acarrearon en el 2010 en el mundo la pérdida de 5,18 millones de años de vida ajustados en función de la discapacidad. A nivel mundial, unos 820 millones de personas están infectadas por lombrices intestinales, 460 millones por tricocéfalos y 440 millones por uncinarias. Aunque cada especie tiene características específicas, para fines de control estas geohelmintiasis se agrupan juntas debido a lo siguiente: (i) son similares su endemicidad geográfica y los grupos vulnerables afectados; (ii) se tratan con los mismos medicamentos; (iii) se utilizan las mismas herramientas para diagnosticarlas; y (iv) sus repercusiones negativas sobre la salud humana obedecen a mecanismos similares (vinculados a la intensidad de la infección). Versión oficial en español de la obra original en inglés. Guideline: preventive chemotherapy to control soil-transmitted helminth infections in at-risk population groups. © Organización Mundial de la Salud 2017. ISBN: 978-92-4-155011-6.

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39

Integrated biological and behavioral surveillance survey (IBBS) among men who have sex with men (MSM) in Kathmandu Valley: Round III--2009. [Kathmandu: STD/AIDS Counseling and Training Services, 2009.

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40

P, Wormser Gary, Stahl Rosalyn E, and Bottone Edward J, eds. AIDS, acquired immune deficiency syndrome, and other manifestations of HIV infection: Epidemiology, etiology, immunology, clinical manifestations, pathology, control, treatment and prevention. Park Ridge, N.J., U.S.A: Noyes Publications, 1987.

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41

Lupton, Joshua. Hospital Acquired Pneumonia. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199976805.003.0023.

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Pneumonia consists of inflammation of the pulmonary parenchyma, typically resulting from a microbial infection. Hospital-acquired pneumonia (HAP) occurs in (typically elderly) patients in long-term care facilities, with regular IV therapy, with immunosuppression, or with a history of recent treatment at a hospital. It is associated with high mortality. The majority HAP patients present with some constellation of cough, fever, sputum production, and pleuritic chest pain. Patients with chronic obstructive pulmonary disease (COPD) and cystic fibrosis are at increased risk for pneumonia. The Infectious Disease Society of America requires infiltrates on chest x-ray or other imaging for the diagnosis of pneumonia. For hospitalized patients, empiric antimicrobial therapy for HAP should be given as soon as pneumonia is highly suspected. There is currently a vaccine available against Streptococcus pneumonia that all patients should be offered before discharge from the hospital. The elderly are already more susceptible to HAP due to decreased mobility and increased comorbidities.

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42

Guidelines for preventing transmission of infection with human T-cell lymphotropic virus type III in the workplace: AIDS. [Olympia?]: Washington State Dept. of Social & Health Services, 1986.

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43

Levy, Barry S., ed. Social Injustice and Public Health. Oxford University Press, 2019. http://dx.doi.org/10.1093/oso/9780190914653.001.0001.

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The third edition of Social Injustice and Public Health provides a comprehensive, up-to-date resource on the relationship of social injustice to the broad field of public health. It includes 29 chapters and many text boxes on a wide range of relevant issues written by 78 contributors who are expert in their respective areas of work. The book includes many descriptions of social injustice and its adverse effects on health, supplemented with many tables, graphs, photographs, and case examples—and many recommendations on what needs to be done to address social injustice. Social Injustice and Public Health is divided into four parts. Part I describes the nature of social injustice and its overall impact on public health. Part II describes how the health of specific population groups is affected by social injustice. Part III describes how social injustice adversely impacts various aspects of health, such as infectious diseases, nutrition, noncommunicable diseases, mental health, and violence. Part IV broadly addresses what needs to be done, from a variety of perspectives, ranging from addressing social injustice in a human rights context, to strengthening communities, to promoting equitable and sustainable human development.

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44

United States. Public Health Service, ed. Summary: Recommendations for preventing transmission of infection with human T-lymphotropic virus type III/lymphadenopathy-associated virus in the workplace. [Rockville, Md.?]: Public Health Service, 1986.

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45

Parkes, Joanna E., Simon Rothwell, and Janine A. Lamb. Aetiology and pathogenesis. Edited by Hector Chinoy and Robert Cooper. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198754121.003.0003.

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The aetiology and pathogenesis of idiopathic inflammatory myopathies (IIM) is poorly understood; IIM are thought to result from exposure to environmental factors in genetically susceptible individuals. Both innate and adaptive immune responses are involved in IIM, and there is increasing evidence that non-inflammatory mechanisms play an important role in disease pathology. Several environmental risk factors, including infectious agents, ultraviolet radiation, cigarette smoking, and exposure to statins, have been implicated. Genetic studies have identified the major histocompatibility complex as the most strongly associated region, while recent large scale genome-wide studies have implicated genes that commonly regulate the adaptive immune response, which overlap with other seropositive autoimmune diseases. Integrating data across these various fields should facilitate refined models of disease pathogenesis.

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46

Family Health International (Organization). Nepal Country Office., New ERA (Firm : Kathmandu, Nepal), and STD/AIDS Counseling and Training Services (Kathmandu, Nepal), eds. Integrated biological and behavioral surveillance survey (IBBS) among male injecting drug users (IDUs) in western to far-western Terai of Nepal: Round III--2009. [Kathmandu: STD/AIDS Counseling and Training Services, 2009.

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47

Katsikis, Peter D., Stephen P. Schoenberger, and Bali Pulendran. Crossroads between Innate and Adaptive Immunity III. Springer, 2011.

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48

Crossroads Between Innate And Adaptive Immunity Iii. Springer, 2011.

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49

Dani, Bolognesi, Abbott Laboratories, University of California, Los Angeles., and Abbott-UCLA Symposium on Human Retroviruses, Cancer, and AIDS: Approaches to Prevention and Therapy (1987 : Keystone, Colo.), eds. Human retroviruses, cancer and AIDS: Approaches to prevention and therapy : proceedings of an Abbott-UCLA Symposium held at Keystone, Colorado, April 1-6, 1987. New York: Liss, 1988.

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50

(Contributor), WHO, ed. Human Immunodeficiency Viruses and Human T-Cell Lymphotropic Viruses (Iarc Monographs on the Evaluation of Carcinogenic Risks to Humans). World Health Organisation, 1997.

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