Neurogenetics
Seiten
1999
Oxford University Press Inc (Verlag)
978-0-19-512975-5 (ISBN)
Oxford University Press Inc (Verlag)
978-0-19-512975-5 (ISBN)
- Titel ist leider vergriffen;
keine Neuauflage - Artikel merken
Intended for physicians who manage patients with inherited diseases of the nervous system, this text presents the clinical phenotypes of the most commonly inherited neurologic diseases, and their molecular pathogenesis, with a description of the appropriate tests to be used in diagnosis.
Neurogenetics is intended for any physician or scientist who manages patients with inherited diseases of the nervous system. It presents the clinical phenotypes of the most commonly inherited neurologic diseases, and their molecular pathogenesis, followed by a description of the appropriate tests to be used in diagnosis. Two introductory chapters familiarize the non-geneticist with medical genetic terminology and molecular genetic techniques useful in the analysis of genetic diseases and genetic testing. Subsequent chapters examine each major genetic neurologic disease.
Neurogenetics is intended for any physician or scientist who manages patients with inherited diseases of the nervous system. It presents the clinical phenotypes of the most commonly inherited neurologic diseases, and their molecular pathogenesis, followed by a description of the appropriate tests to be used in diagnosis. Two introductory chapters familiarize the non-geneticist with medical genetic terminology and molecular genetic techniques useful in the analysis of genetic diseases and genetic testing. Subsequent chapters examine each major genetic neurologic disease.
1. Introductioin to Medical Genetics; 2. Molecular Techniques; 3. Strategies Towards Cloning Of Disease Genes; 4. Familial Alzheimer Disease; 5. ALS; 6. Hereditary Motor Sensory Neuropathies; 7. Duchenne Muscular Dystrophy; 8. FSH and DM; 9. Huntington Disease; 10. Dominant Atazias; 11. Neurofibromatoses; 12. Mitochondrial Diseases; 13. Prion Diseases; 14. Wilson's and Menke's Disease; 15. Metachromatoic Leukodystrophy; 16. Neuronal Ceroid Lipofuscinoses; 17. Gene Dosage and Disease: Trisomy 21; 18. Holoprosencephaly; 19. Parkinson's; 20. Epilepsy; 21. Migraine; 22. Stroke; 23. Chromosomal Map of Neurologic Diseases
Erscheint lt. Verlag | 4.11.1999 |
---|---|
Verlagsort | New York |
Sprache | englisch |
Gewicht | 1080 g |
Themenwelt | Medizin / Pharmazie ► Medizinische Fachgebiete ► Neurologie |
Studium ► 2. Studienabschnitt (Klinik) ► Anamnese / Körperliche Untersuchung | |
Studium ► 2. Studienabschnitt (Klinik) ► Humangenetik | |
ISBN-10 | 0-19-512975-X / 019512975X |
ISBN-13 | 978-0-19-512975-5 / 9780195129755 |
Zustand | Neuware |
Haben Sie eine Frage zum Produkt? |
Mehr entdecken
aus dem Bereich
aus dem Bereich
aus Klinik und Praxis
Buch | Softcover (2023)
Urban & Fischer (Verlag)
42,00 €
Buch | Hardcover (2017)
Hogrefe (Verlag)
60,00 €
Buch | Softcover (2024)
Urban & Fischer in Elsevier (Verlag)
56,00 €