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Libri sul tema "Hepatitis B"

Autore: Grafiati

Pubblicato: 4 giugno 2021

Ultima modifica: 31 luglio 2024

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1

Royal Colleges of Physicians of the United Kingdom. Committee on Health Promotion. Hepatitis B (serum hepatitis). London: Faculty of Community Medicine of the Royal Colleges of Physicians of the United Kingdom, 1985.

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2

Freedman, Jeri. Hepatitis B. New York: Rosen, 2009.

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3

Branch, Canada Health Protection. Hepatitis B. [Ottawa]: Health Protection Branch, 1991.

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4

J, Gerety R., a cura di. Hepatitis B. Orlando: Academic Press, 1985.

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5

Massachusetts. Department of Public Health. Hepatitis B. Boston, MA: Massachusetts Dept. of Public Health, 1987.

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6

Ozaras, Resat, e Veysel Tahan, a cura di. Viral Hepatitis: Chronic Hepatitis B. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-93449-5.

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7

Guo, Haitao, e Andrea Cuconati, a cura di. Hepatitis B Virus. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6700-1.

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8

Ohio. Perinatal Hepatitis B Prevention e California. Dept. of Health, a cura di. Hepatitis B & pregnancy. Columbus: Ohio Department of Health, 2002.

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9

Guo, Haitao, e Andrea Cuconati, a cura di. Hepatitis B Virus. New York, NY: Springer US, 2024. http://dx.doi.org/10.1007/978-1-0716-4027-2.

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10

Rajen, Koshy, e Caselmann Wolfgang H, a cura di. Hepatitis B virus: Molecular mechanisms in disease and novel strategies for therapy. London: Imperial College Press, 1998.

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11

Tang, Hong, a cura di. Hepatitis B Virus Infection. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-13-9151-4.

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12

1946-, Callea F., Zorzi M. 1920-, Desmet V, Associazione volontari italiani del sangue. Brescia Division. e Postgraduate Course on Viral Hepatitis (1985 : Brescia, Italy), a cura di. Viral hepatitis. Berlin: Springer-Verlag, 1986.

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13

1953-, Hamatake Robert Kiyoshi, e Lau Johnson Y. N, a cura di. Hepatitis B and D protocols. Totowa, N.J: Humana Press, 2004.

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14

National Digestive Diseases Information Clearinghouse (U.S.), a cura di. What I need to know about Hepatitis B. Bethesda, Md: Nattional Institutes of Health, National Digestive Diseases Information Clearinghouse, 2000.

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15

National Digestive Diseases Information Clearinghouse (U.S.), a cura di. Lo que necesito saber sobre la Hepatitis B. Bethesda, Md: Institutos Nacionales De Salud, Centro Coordinador Nacional de Información Sobre las Enfermedades Digestivas, 1999.

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16

National Digestive Diseases Information Clearinghouse (U.S.), a cura di. Lo que necesito saber sobre la hepatitis B: What I need to know about hepatitis B. [Bethesda, Md.]: U.S. Dept. of Health and Human Services, National Institutes of Health, National Digestive Diseases Information Clearinghouse, 2004.

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17

Council, Pakistan Medical Research. Prevalence of hepatitis B & C in Pakistan. Islamabad: Pakistan Medical Research Council, 2009.

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18

Everson, Gregory T. Living with hepatitis B: A survivor's guide. New York: Hatherleigh Press, 2002.

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19

Hamatake, Robert K., e Johnson Y. N. Lau. Hepatitis B and D Protocols. New Jersey: Humana Press, 2004. http://dx.doi.org/10.1385/159259669x.

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20

Hamatake, Robert K., e Johnson Y. N. Lau. Hepatitis B and D Protocols. New Jersey: Humana Press, 2004. http://dx.doi.org/10.1385/1592596703.

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21

1968-, Zhang Weiying, e Ye Lihong, a cura di. Hepatitis B virus research focus. New York: Nova Science Publishers, 2008.

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22

Centers for Disease Control (U.S.), a cura di. Hepatitis B prevention and pregnancy: How to protect your baby against hepatitis B. Atlanta, Ga: Hepatitis Branch, Division of Viral and Rickettsial Diseases, National Center for Infectious Diseases, Centers for Disease Control, 1994.

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23

Lindh, Gudrun. Chronic hepatitis B: Impact of hepatitis D virus superinfection and the hepatitis B e-system on histological outcome, and correlation of the hepatitis B e-system to HBV-DNA in serum. Stockholm: Distributed by the Almqvist & Wiksell Periodical Co., 1986.

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24

institutet, Karolinska, a cura di. Chronic hepatitis B: Impact of hepatitis D virus superinfection and the hepatitis B e-system on histological outcome, and correlation of the hepatitis B e-system to HBV-DNA in serum. Stockholm, Sweden: Distributed by Almqvist & Wiksell Periodical Co., 1986.

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25

Alan, McLachlan, a cura di. Molecular biology of the hepatitis B virus. Boca Raton, Fla: CRC Press, 1991.

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26

David, Ikpokpo. Hepatitis Series: Hepatitis a & Hepatitis B. Independently Published, 2019.

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27

Bansal, Sanjay. Hepatitis B. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198759928.003.0063.

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Abstract (sommario):

The chapter on hepatitis B discusses the epidemiology and transmission of this infection. It covers the clinical features, complications, and prevention of the disease, but also the interpretation of the serology as well the management of the chronic hepatitis B infection.

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28

Beattie, R. Mark, Anil Dhawan e John W.L. Puntis. Hepatitis B. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198569862.003.0057.

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Abstract (sommario):

Epidemiology 418Transmission 418Clinical features 418Interpretation of HBV serology 419Complications 419Prevention 421Management of chronic HBV infection 422• About 2 billion people (1/3 of the world population) show evidence of exposure to hepatitis B virus (HBV) infection, with 300–400 million showing evidence of chronic HBV infection....

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29

Muche, Marion, e Seema Baid-Agrawal. Hepatitis B. A cura di Vivekanand Jha. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0185_update_001.

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Hepatitis B virus (HBV) has been causally linked to a variety of renal diseases, the most common being glomerular diseases and systemic autoimmune disease. Membranous nephropathy (MN) is the commonest HBV-associated glomerulonephritis (HBV-GN), followed by membranoproliferative glomerulonephritis (MPGN), mesangial proliferative glomerulonephritis, immunoglobulin (Ig)-A nephropathy, and focal segmental glomerulosclerosis (FSGS). Polyarteritis nodosa is a rare manifestation. The incidence of HBV-associated renal diseases seems to be decreasing with the introduction of vaccination programmes.HBV-MN is the most frequent cause of nephrotic syndrome in children in countries with high endemicity of HBV infection. The clinical course is usually benign in children with high rates of spontaneous remission rates and low risk of progression to renal failure. The prognosis is worse in adults. Of the systemic autoimmune disorders associated with HBV infection that involve the kidneys, the strongest link has been found with polyarteritis nodosa (PAN), a lesion that causes arteritis of medium-sized renal vessels. HBV-associated PAN (HBV-PAN) usually manifests in the first year after infection, and is clinically indistinguishable from classic PAN.Diagnosis of HBV-GN or -PAN is based on the clinical picture, histological findings, evidence of viral replication in serum and/or liver and detection of HBV antigens or DNA in the tissue. Besides deposition of immune complexes, other mechanisms such as virus-induced cytopathic damage have been proposed to explain the pathogenesis.HBV-GN and HBV-PAN appear to respond to antiviral treatment. Both show remission after HBeAg seroconversion. The available studies predominantly employed first-generation agents like interferon alpha and lamivudine, which showed suppression of viral replication and clinical remission of HBV-associated renal disease. Immunosuppressive therapy appears to be inevitable for the control of severe HBV-PAN and could be helpful in addition to antiviral treatment for cases of HBV-GN not responding clinically to antiviral treatment.

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30

Huyton, Rita, Sam Ghebrehewet e David Baxter. Hepatitis B. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198745471.003.0006.

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This chapter describes an acute hepatitis B case and scenario involving a paramedic with a pregnant woman as close sexual contact and potential risk of transmission to the unborn baby. Background information on the epidemiology of Hepatitis B, markers of hepatitis B infection (both acute and chronic), and the risk factors for transmission are discussed. There are clear case definitions of acute, chronic, and those susceptible and at high risk for hepatitis B plus detailed interpretation of hepatitis B markers. ‘Top tips’ are given to assist the relevant clinicians or public health/health protection practitioner/specialist to take timely and appropriate action. The laboratory, epidemiological, and infection prevention and control components of the investigation are listed. The importance of confidentiality and communication with the affected individual and close contacts is emphasized. Other possible scenarios, including the public health response to a cluster/outbreak are considered.

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31

Hepatitis B. London: Health Promotion England, 2000.

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32

Tintoré, Joaquín Balanzó. Hepatitis B. Marge Médica Books, 2007.

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33

Freedman, Jeri. Hepatitis B. Rosen Publishing Group, 2009.

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34

Rodrigo, Luis. Hepatitis B. IntechOpen, 2022.

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35

Parliament, Canada. Hepatitis B. Ottawa, 1992.

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36

Hepatitis B. Rosen Publishing Group, 2009.

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37

Hepatitis B. Rosen Publishing Group, 2009.

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38

Ozaras, Resat, e Veysel Tahan. Viral Hepatitis: Chronic Hepatitis B. Springer, 2018.

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39

Chronic Hepatitis B. W.B. Saunders Company, 2010.

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40

Kourtis, Athena P., Shruti Chandramouli, Gonzague Jourdain e Marc Bulterys. Hepatitis B Virus. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190604813.003.0004.

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Abstract (sommario):

Hepatitis B virus (HBV) is the most common cause of chronic viral hepatitis and hepatocellular carcinoma in the world. Worldwide, more than 250 million people are chronically infected with HBV, causing nearly 780,000 deaths each year, and mother-to-child transmission (MTCT) accounts for more than one-third of chronic HBV infections. Universal vaccination in neonates is the most effective strategy for eliminating infections worldwide. Maternal antiviral treatment during the antepartum/postpartum period for mothers with high HBV viral loads is effective in preventing HBV MTCT. Full immunization coverage is currently the only way to reach the goal of eradicating HBV infection. Operational research and, in some resource-limited settings, international funding may be essential to bring the vaccine where neonates and infants need it, including remote locations where home births are common. Continued improvements in the coverage and timeliness of HBV vaccination and education of clinicians about its importance are needed.

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41

Koshy, Rajen, e Wolfgang H. Caselmann. Hepatitis B Virus. PUBLISHED BY IMPERIAL COLLEGE PRESS AND DISTRIBUTED BY WORLD SCIENTIFIC PUBLISHING CO., 1998. http://dx.doi.org/10.1142/p005.

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42

About hepatitis B. Alton: Scriptographic Publications, 1996.

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43

Hepatitis B & pregnancy. Columbus: Ohio Department of Health, 2002.

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44

About hepatitis B. Haslemere: Scriptographic Publications, 1989.

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45

Cox, Jeffrey T., e Dedrick I. Owen. Hepatitis B: New Research. Nova Science Publishers, Incorporated, 2013.

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46

Hepatitis B: The hunt for a killer virus. Princeton, N.J: Princeton University Press, 2002.

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47

Poynard, Thierry. Hepatitis B and C. CRC Press, 2001. http://dx.doi.org/10.1201/9780367801861.

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48

Poynard, Thierry. Hepatitis B and C. CRC Press, 2001. http://dx.doi.org/10.1201/9781420047165.

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49

Poynard, Thierry. Hepatitis B and C. CRC Press, 2004. http://dx.doi.org/10.4324/9780203357187.

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50

Hepatitis B [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.95726.

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