Huntington's disease has received considerable attention from the scientific community in recent decades. Despite this, the molecular mechanisms related to the genesis of the disorder are still not sufficiently clear. It is known to be an autosomal dominant disease of complete penetrance occurring in the specific gene on chromosome four. The pathology is generally characterized by late onset and its clinical manifestations (motor disorders, psychiatric and cognitive disturbances) dramatically affect the quality of life of patients.Many therapeutic strategies have been tested, but the complexity of the multiple mechanisms leading to the neurodegeneration observed in the disease contribute to the lack of success in the search for an effective treatment. It is a disease with progressive evolution and there is still no specific treatment available, however an adequate orientation of the person and his family on the benefits of a correct diet, practice of rehabilitation exercises and pharmacological treatment contribute to improve their quality of life.
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Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Huntington's disease has received considerable attention from the scientific community in recent decades. Despite this, the molecular mechanisms related to the genesis of the disorder are still not sufficiently clear. It is known to be an autosomal dominant disease of complete penetrance occurring in the specific gene on chromosome four. The pathology is generally characterized by late onset and its clinical manifestations (motor disorders, psychiatric and cognitive disturbances) dramatically affect the quality of life of patients.Many therapeutic strategies have been tested, but the complexity of the multiple mechanisms leading to the neurodegeneration observed in the disease contribute to the lack of success in the search for an effective treatment. It is a disease with progressive evolution and there is still no specific treatment available, however an adequate orientation of the person and his family on the benefits of a correct diet, practice of rehabilitation exercises and pharmacological treatment contribute to improve their quality of life. 52 pp. Englisch. N° de réf. du vendeur 9786205226261
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Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -Huntington's disease has received considerable attention from the scientific community in recent decades. Despite this, the molecular mechanisms related to the genesis of the disorder are still not sufficiently clear. It is known to be an autosomal dominant disease of complete penetrance occurring in the specific gene on chromosome four. The pathology is generally characterized by late onset and its clinical manifestations (motor disorders, psychiatric and cognitive disturbances) dramatically affect the quality of life of patients.Many therapeutic strategies have been tested, but the complexity of the multiple mechanisms leading to the neurodegeneration observed in the disease contribute to the lack of success in the search for an effective treatment. It is a disease with progressive evolution and there is still no specific treatment available, however an adequate orientation of the person and his family on the benefits of a correct diet, practice of rehabilitation exercises and pharmacological treatment contribute to improve their quality of life.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 52 pp. Englisch. N° de réf. du vendeur 9786205226261
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Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Huntington's disease has received considerable attention from the scientific community in recent decades. Despite this, the molecular mechanisms related to the genesis of the disorder are still not sufficiently clear. It is known to be an autosomal dominant disease of complete penetrance occurring in the specific gene on chromosome four. The pathology is generally characterized by late onset and its clinical manifestations (motor disorders, psychiatric and cognitive disturbances) dramatically affect the quality of life of patients.Many therapeutic strategies have been tested, but the complexity of the multiple mechanisms leading to the neurodegeneration observed in the disease contribute to the lack of success in the search for an effective treatment. It is a disease with progressive evolution and there is still no specific treatment available, however an adequate orientation of the person and his family on the benefits of a correct diet, practice of rehabilitation exercises and pharmacological treatment contribute to improve their quality of life. N° de réf. du vendeur 9786205226261
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Taschenbuch. Etat : Neu. The Person with Huntington's Disease | Functional and Cognitive Evaluation | Hugo Moita Dos Santos (u. a.) | Taschenbuch | Englisch | 2022 | Our Knowledge Publishing | EAN 9786205226261 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu. N° de réf. du vendeur 125742159
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