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Genetics and Neurology

Buch | Hardcover
460 Seiten
1992 | 2nd Revised edition
Churchill Livingstone (Verlag)
978-0-443-04523-3 (ISBN)
133,40 inkl. MwSt
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Offering guidance to clinical geneticists and neurologists about the mode of inheritance and genetic counselling risks for neurological conditions, this text groups subjects together under such headings as the muscular dystrophies, phakomatoses, peripheral neuropathies, and dementias. The author incorporates the advances in molecular biology that have occurred in the past 7 years and the localization of genes for many neurological disorders. A new chapter on mitochondrial diseases is included, as well as new sections on the Xp21 muscular dystrphies, the chronic spinal muscular atrophies, amyloid neuropathies, Rett's syndrome, torsion dystonia, trichothiodystrophy, early onset Cockayne syndrome and prion protein diseases. New descriptions of unusual genetic mechanisms are provided and 18 new illustrations and a map of the chromosomal locations of some neurological diseases are given.

Malformations of the central nervous system; phakomatoses and tumours; cerebral degenerative disorders of childhood; extrapyramidil disorders and dyskinesia; muscle disorders I; muscle disorders II; mitochondrial diseases; spinal muscular atrophies (SMAs); hereditary neuropathies; cerebellar and spinocerebellar ataxias; spastic paraplegias; neurological diseases in which there are defects in DNA repair of synthesis; multifactorial inheritance and neurological diseases; dementia and epilepsy.

Erscheint lt. Verlag 8.6.1992
Reihe/Serie Genetics in Medicine & Surgery S.
Vorwort Alan E.H. Emery
Zusatzinfo 16 line drawings and 55 half-tone illustrations, index
Verlagsort London
Sprache englisch
Maße 287 x 33 mm
Gewicht 1035 g
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Neurologie
Studium 2. Studienabschnitt (Klinik) Humangenetik
ISBN-10 0-443-04523-2 / 0443045232
ISBN-13 978-0-443-04523-3 / 9780443045233
Zustand Neuware
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