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• W3214157032 abstract "Studies in personalized medicine are based on the concept that in individual patients diagnosed with the same disease there are frequently different underlying causative factors. These can include different genetic and genomic factors. Based on these differences different patients may therefore respond differently to therapy. In this chapter different underlying genetic factors are explored in certain childhood disease and different adult diseases. These include epilepsy, cerebral palsy, and movement disorders, particularly forms of ataxia. Underlying etiologic factors are presented in specific adult diseases including hypertension, coronary heart disease, and hyperlipidemias. The value of genetic and genomic studies to establish diagnosis in disorders in the undiagnosed disease category are also presented." @default.
• W3214157032 created "2021-11-22" @default.
• W3214157032 creator A5091712099 @default.
• W3214157032 date "2022-01-01" @default.
• W3214157032 modified "2023-10-16" @default.
• W3214157032 title "Benefits of the incorporation of genomic medicine in clinical practice" @default.
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• W3214157032 doi "https://doi.org/10.1016/b978-0-323-91547-2.00001-4" @default.
• W3214157032 hasPublicationYear "2022" @default.
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