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    This has shifted the responsibility for many medical tasks to family caregivers. They have become frontline workers and should be treated as members of the patient's health care team.

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    First-degree relatives share one half of their genes in common. A second-degree relative includes aunts, uncles, nieces, nephews, half-siblings, and grandparents.

    Second-degree relatives share one quarter of their genes in common. Family health history information includes disease history of a subject's biological relatives.

    For example, family health history information can include disease history of first- and second-degree relatives, as well as disease history of more distant relatives.

    Disease history, for example, can include the number of first- and second-degree relatives, if a relative has or has had a disease of interest, indicator disease or indicator trait, sex of affected relatives, lineage of affected relatives e.

    Personal health behavior information includes information related to smoking, exercise, diet, screening tests, and the like. Screening tests include any test that screens for disease or risk factors associated with disease.

    For example, screening tests can include clinical breast exams, mammograms, fecal occult blood tests, sigmoidoscopy, colonoscopy, blood cholesterol test, blood pressure test, blood sugar test, and the like.

    Familial risk of disease includes a likelihood of developing a disease based on personal and family health histories. In other words, the familial risk of disease describes the strength of the personal and family health histories as a risk factor for a disease of interest.

    For example, familial risk of a disease of interest can be categorized as high e. For most common diseases, compared to weak familial risk, having a moderate familial risk may be associated with about a 2-fold increase, and having a strong familial risk may be associated with about a 3-fold or greater increase in risk.

    A predetermined personal disease history scenario includes any personal health history information that may be associated with increased or decreased risk for a disease of interest.

    For example, having a personal history of a disease of interest at an early age of onset and having an indicator trait can be a predetermined personal disease history scenario, and having a personal history of an indicator disease associated with a disease of interest at a late age of onset can be a predetermined personal disease history scenario.

    A predetermined familial disease history scenario includes any family health history information that may be associated with increased or decreased risk for a disease of interest.

    For example, having a first-degree relative with a disease of interest at a late age of onset can be a predetermined familial disease history scenario, and having two second-degree relatives from the same lineage with an indicator disease at an early age of onset is another example of a predetermined familial disease history scenario.

    Intersection of predetermined personal and familial disease history scenarios includes situations in which the predetermined personal and familial disease history scenarios are referenced with one ore more familial risk matrices for the disease of interest.

    According to an embodiment of the invention, for any given predetermined personal disease history scenario, a minimum of two predetermined familial disease history scenarios that describe family history information will meet in a familial risk-indicating cell within the matrix.

    The level of familial risk e. Note that for any given predetermined personal disease history scenario the assigned familial risk of disease of interest could be based on several intersections obtained from several different predetermined familial disease history scenarios identified within a matrix for a disease of interest.

    In that case, the cell with the highest magnitude of risk is selected in order to assign the familial risk of disease.

    Familial risk clarifiers include qualifying statements, which clarify or further explain the assignment of familial risk of a disease of interest by describing the elements of the personal or family history that are associated with the level of familial risk, and the possibility that the personal and family histories are suggestive of an inherited syndrome.

    For example, familial risk clarifiers can be used in the explanation of familial risk to subjects and health professionals, can inform genetic testing decisions, and can be used to tailor a disease prevention plan.

    In any of the examples herein, an age of onset of disease or age at first diagnosis of a disease or trait can be an age range, particular age, age category e.

    Although particular ages are shown in some examples e. At , personal and family health histories are collected. For example, disease history of a subject and a subject's first- and second-degree biological relatives can be collected, including the sex of the subject, and the number, sex, type and lineage of the subject's first- and second-degree relatives, and whether the subject or a relative has or has had the disease of interest, or an indicator disease or indicator trait associated with that disease of interest, and the age of the subject and relative at the time of first diagnosis or onset of the disease of interest, indicator disease or indicator trait.

    At , familial risk of the disease of interest is determined by analyzing personal and family health histories.

    For example, predetermined personal and familial disease history scenarios can be analyzed. At , results of the determination of the familial risk of a single disease of interest are presented.

    For example, the familial risk of a disease of interest can be presented as high e. Familial risk clarifiers can also be presented.

    The method described in this or any of the other examples can be a computer-implemented method performed via computer-executable instructions in one or more computer-readable media.

    Any of the actions shown can be performed by software incorporated within an electronic medical record system or any other health information system, or a database supporting clinical trials or epidemiologic research.

    At , personal and family health histories of a subject are received. For example, disease history of a subject and a subject's first- and second-degree biological relatives can be received, including the number, lineage, type and sex of first- and second-degree relatives, and whether the subject or a relative has or has had diseases of interest, or an indicator disease or an indicator trait associated with those diseases of interest, and the age of the subject and relatives at the time of first diagnosis or onset of the diseases of interest, indicator diseases or indicator traits.

    At , a disease of interest is determined. For example, heart disease, stroke, diabetes, colorectal cancer, breast cancer, and ovarian cancer can be diseases of interest that are determined.

    At , the familial risk of the determined disease of interest can be assigned for a subject. For example, the personal health history of a subject and the family health history of a subject's first- and second-degree biological relatives can be analyzed to assign the level of familial risk for the disease of interest.

    Following the assignment of the familial risk for the determined disease of interest, one or more additional diseases of interest can be determined at , and the level of familial risk for the one or more additional diseases of interest can be assigned.

    At , results of the assignment of the familial risk for the one or more diseases of interest can be presented. For example, the familial risk can be categorized as low e.

    At , personal and family health histories for a subject are obtained. Personal and family health histories can be obtained in real-time from the subject or another historian e.

    For example, personal and family health histories for a subject can be obtained via completed questionnaires in an electronic or paper format.

    Tasch Professor in Parkinson Disease Research Director of the Movement Disorder Program UC San Diego "DSM V: a view from the inside" Joel E. Dimsdale, M.

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    Squire, Ph. Distinguished Professor of Psychiatry, Neurosciences, and Psychology UC San Diego School of Medicine Research Career Scientist VA Medical Center, San Diego "Duchenne Muscular Dystrophy: Today and Tomorrow" Robert Leshner, M.

    D HHMI Investigator Professor-Salk Institute La Jolla, CA "Development of CNS Therapeutics in the era of translational medicine" Richard Smith, M.

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    Assistant Professor Department of Neurosciences University of California, San Diego "Current and Future Intervention for Stroke: A Surgical Disease" Elad L.

    Professor Department of Molecular and Experimental Medicine The Scripps Research Institute "New Developments in Parkinson Disease" Peter LeWitt, M.

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    However, the initial success of the band was short lived as Parkinson became victim to the side effects of molecular digitization and left Memphis in search of Dr.

    AWO enlisted the help of veteran drummer Chris Craig of Black Oak Arkansas and Lord Tracy. This lo-fi rock anthem captures the spirit and feel of an old rock show at an auditorium full of sex dolls.

    His spaceship crash landed deep in the heart of Memphis after a few cosmic collisions with New York and Nashville.

    Backed by local misfits and sometime-legends, he has become know for his all-night, bar-dancing, guitar-levitating, brown-liquor-down-the-back-of-your-throat live shows.

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    He has been making terrible music since the late s, mostly in Memphis, Tennessee. This is just another horrible record by an equally horrible man except that the late, great Jim Dickinson performs on it for inexplicable reasons.

    This track almost sounds like music when Jim is singing and playing guitar. Caveat emptor indeed. Born and raised in Little Rock , Arkansas the land of giants, by the way , lady T first hit the Memphis scene in and soon joined the forces with the Hellcats as percussionist and later as drummer for those wild spirited gals.

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    Life timeline of Martha Hartwig Scheuner. Martha Hartwig Scheuner was born on 10 May Martha Hartwig Scheuner was 6 years old when Thomas Edison patents the motion picture camera.

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