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Libros sobre el tema "Genetic risk of disease"

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1

Petrakis, Peter L. Alcoholism, and inherited disease. Rockville, Md: U.S. Dept. of Health and Human Services, Public Health Service, Alcohol, Drug Abuse, and Mental Health Administration, National Institute on Alcohol Abuse and Alcoholism, 1985.

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2

J, Alberts Mark, ed. Genetics of cerebrovascular disease. Armonk, NY: Futura Pub. Co., 1999.

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3

Uri, Goldbourt, De Faire Ulf y Berg Kåre, eds. Genetic factors in coronary heart disease. Dordrecht: Kluwer Academic, 1994.

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4

Kåre, Berg, ed. Genetic approaches of coronary heart disease and hypertension. Berlin: Springer-Verlag, 1991.

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5

Gormley, Myra Vanderpool. Family diseases: Are you at risk? Baltimore, MD: Genealogical Pub. Co., 1989.

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6

Ueland, Per Magne y Rima Rozen. MTHFR polymorphisms and disease. Georgetown, Tex: Landes Bioscience, 2005.

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7

Magne, Ueland Per y Rozen Rima, eds. MTHFR polymorphisms and disease. Georgetown, Tex: Landes Bioscience/ Eurekah.com, 2005.

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8

Mapping fate: A memoir of family, risk, and genetic research. New York: Times Books, 1995.

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9

Wexler, Alice. Mapping fate: A memoir of family, risk, and genetic research. Berkeley: University of California Press, 1995.

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10

Genetic susceptibility to cancer. Boston: Kluwer Academic, 1998.

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11

A, Bray George y Ryan Donna H, eds. Nutrition, genetics, and heart disease. Baton Rouge: Louisiana State University Press, 1996.

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12

Dimond, Rebecca y Jamie Lewis. Analysing Semi-Structured Interviews: Understanding Family Experience of Rare Disease and Genetic Risk. 1 Oliver's Yard, 55 City Road, London EC1Y 1SP United Kingdom: SAGE Publications, Ltd., 2015. http://dx.doi.org/10.4135/9781473947467.

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13

United States. Congress. Office of Technology Assessment., ed. Genetic monitoring and screening in the workplace. Washington, DC: Congress of the U.S., Office of Technology Assessment, 1990.

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14

Offit, Kenneth. Clinical cancer genetics: Risk counseling and management. New York: Wiley-Liss, 1998.

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15

Hiroshi, Hiai y Hino Okio, eds. Animal models of cancer predisposition syndromes. Basel: Karger, 1999.

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16

Risk factors for cerebrovascular disease and stroke. Oxford: Oxford University Press, 2016.

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17

1960-, Foulkes William D. y Hodgson S. V, eds. Inherited susceptibility to cancer: Clinical, predictive, and ethical perspectives. Cambridge: Cambridge University Press, 1998.

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18

1955-, Walker Cheryl, ed. Genetics and cancer susceptibility: Implications for risk assessment. New York: Wiley-Liss, 1996.

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19

National Cancer Institute (U.S.) y National Action Plan on Breast Cancer (Organization : U.S.), eds. Genetic testing for breast cancer risk: It's your choice. Bethesda, MD: National Cancer Institute, 1999.

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20

H, Benum Sara, ed. Genetic nutritioneering. Los Angeles: Keats Pub., 1998.

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21

Batsheva, Bonné-Tamir y Adam Avinoam, eds. Genetic diversity among Jews: Diseases and markers at the DNA level. New York: Oxford University Press, 1992.

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22

Negotiating risk: British Pakistani experiences of genetics. New York: Berghahn Books, 2009.

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23

International, Conference on Carcinogenesis and Risk Assessment (8th 1994 Austin Tex ). Genetics and cancer susceptibility: Implications for risk assessment : proceedings of the Eighth International Conference on Carcinogenesis and Risk Assessment, held in Austin, Texas, November 30-December 3, 1994. New York: Wiley-Liss, 1996.

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24

Great Britain. Genetics and Insurance Committee. Decision of the Genetics and Insurance Committee (GAIC) concerning the application for approval to use genetic test results for life insurance risk assessment in Huntington's disease. [London]: Department of Health, 2000.

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25

P, Newnham John y Ross Michael G, eds. Early life origins of human health and disease. Basel: Karger, 2009.

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26

Uehara Memorial Foundation Symposium on Common Disease (1999 Tokyo). Common disease: Genetic and pathogenetic aspects of multifactorial diseases, proceedings of the Uehara Memorial Foundation Symposium on Common Disease, Tokyo on June 30-July 2, 1999. Editado por Imura Hiroo, Kasuga Masato y Nakao Kazuwa 1948-. Amsterdam: Elsevier Science B.V., 1999.

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27

The Apoe gene diet: A breakthrough in lowering cholesterol, weight, and the risk of cardiovascular and Alzheimer's disease through knowledge of your body's genes. Santa Rosa, CA: Elite Books, 2007.

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28

Hodgson, S. V. A practical guide to human cancer genetics. Cambridge [England]: Cambridge University Press, 1993.

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29

V, Hodgson S., ed. A practical guide to human cancer genetics. 3a ed. Cambridge: Cambridge University Press, 2007.

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30

National Cancer Institute (U.S.). Clinical Genetics Branch. Inherited bone marrow failure syndromes: Studying families with rare blood disorders and risk of cancer. Bethesda, Md.]: U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, National Cancer Institute, Division of Cancer Epidemiology and Genetics, Clinical Genetics Branch, 2002.

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31

National Research Council (U.S.). Committee on Genetically Modified Pest-Protected Plants., ed. Genetically modified pest-protected plants: Science and regulation. Washington, D.C: National Academy Press, 2000.

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32

National Council on Radiation Protection and Measurements. Potential impact of individual genetic susceptibility and previous radiation exposure on radiation risk for astronauts. Bethesda, Md: National Council on Radiation Protection and Measurements, 2011.

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33

The calculation of genetic risks: Worked examples in DNA diagnostics. 2a ed. Baltimore: Johns Hopkins University Press, 1997.

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34

Frohlich, Edward D. Take heart: Cut your inherited risks of heart disease. New York: Crown Publishers, 1990.

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35

1961-, Rodríguez Santiago, ed. Genetic endocrinology of the metabolic syndrome. Hauppauge NY: Nova Science Publishers, 2009.

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36

To test or not to test: A guide to genetic screening and risk. New Brunswick, N.J: Rutgers University Press, 2008.

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37

Teichler-Zallen, Doris. To test or not to test: A guide to genetic screening and risk. New Brunswick, N.J: Thorndike Press, 2009.

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38

Prophylactic mastectomy: Insights from women who chose to reduce their risk. Santa Barbara, Calif: Praeger, 2012.

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39

The calculation of genetic risks: Worked examples in DNA diagnostics. Baltimore: Johns Hopkins University Press, 1994.

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40

1947-, Lusis Aldons J., Rotter Jerome I y Sparkes Robert S. 1930-, eds. Molecular genetics of coronary artery disease: Candidate genes and processes in atherosclerosis. Basel: Karger, 1992.

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41

Proceed with caution: Predicting genetic risks in the recombinant DNA era. Baltimore: Johns Hopkins University Press, 1989.

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42

1952-, Andrews Lori B., ed. Assessing genetic risks: Implications for health and social policy. Washington, D.C: National Academy Press, 1994.

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43

Macular degeneration: Causes, diagnosis and treatment. New York: Nova Science Publishers, 2011.

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44

Experimental man: What one man's body reveals about his future, your health, and our toxic world. Hoboken, N.J: Wiley, 2009.

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45

Seshadri, Sudha y Stéphanie Debette, eds. Risk Factors for Cerebrovascular Disease and Stroke. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199895847.001.0001.

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Risk Factors for Cerebrovascular Disease and Stroke describes environmental and genetic determinants for cerebrovascular disease and stroke from the perspective of an international group of neurologists, epidemiologists, and geneticists who are at the forefront of research and education on these issues. Unlike other books in the field, which solely deal with physiology, diagnosis, and management of stroke, this essential book discusses prevention factors as well as the causes. This unique book takes a comprehensive approach to risk prediction while integrating epidemiological, genetic, and statistical principles explained in a way that is easy for the clinical trainee to understand. The section on genetic risk factors for various types of stroke is unique in its depth and up-to-date information. Clinicians, residents, fellows and academics in neurology, geriatrics, internal medicine, epidemiology, genetics, public health professionals, and preventative cardiologists, as well as nurses, practitioners and physician assistants will find this a handy source for years to come.
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46

Ueland, Per Magne. MTHFR Polymorphisms and Disease. Taylor & Francis Group, 2005.

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47

Mapping Fate: A Memoir of Family, Risk, and Genetic Research. University of California Press, 1996.

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48

Banerjee, Amitava y Kaleab Asrress. Risk factors for cardiovascular disease. Editado por Patrick Davey y David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0086.

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The most prevalent cardiovascular diseases (CVDs) are atherosclerotic, affecting all arterial territories. Epidemiologic studies such as the Framingham and INTERHEART studies have firmly established the commonest or ‘traditional’ risk factors for CVD; namely, smoking, hypertension, diabetes mellitus, hypercholesterolaemia, and a family history of CVD. The ‘risk-factors approach’ to CVD looks at these factors, individually and in combination, in the causation of disease. The complex causation pathways involve interplay of individual factors, whether genetic or environmental. More recently, there has been increasing interest in ‘epigenetics’ or the way in which the environment interacts with genes in the process underlying CVD. This chapter presents an analysis of the traditional and novel risk factors for CVD.
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49

Common Disease - Genetic and Pathogenetic Aspects of Multifactorial Diseases. Elsevier Science Pub Co, 1999.

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50

Fiona, Lalloo, ed. Risk assessment and management in cancer genetics. Oxford: Oxford University Press, 2005.

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