Neuromuscular Disorders

Clinical and Molecular Genetics

Buch | Hardcover

512 Seiten

1998
John Wiley & Sons Ltd (Verlag)
978-0-471-97817-6 (ISBN)

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This text presents a comprehensive overview of the current understanding of the molecular pathology of neuromuscular disorders. For each of 20 disorders, international authorities in the field offer reviews, including: clinical features, pathology, inheritance and molecular genetics.

This text presents a comprehensive overview of the current understanding of the molecular pathology of neuromuscular disorders. For each of 20 disorders, the leading international authorities in the field review: clinical features, pathology, inheritance, molecular genetics, screening, prenatal diagnosis, prevention and counselling, and possible treatment by drug or gene therapy.

Molecular genetics of muscular disorders; congenital muscular dystrophies; Duchenne & Becker muscular dystrophies; Emery-Dreifuss muscular dystrophy; facioscapulohueral muscular dystrophy; limb girdle muscular dystrophies; oculo-pharyngeal muscular dystrophy; distal myopathies and related disorders; mitochondrial myopathies; central core disease; desminopathies; nemaline myopathy; myotubular myopathy; fibrodysplasia ossificans progressiva; myotonic dystrophy; non-dystrophic myotonias; spinal muscular atrophy; familial ALS; congenetial myasthenic syndromes; hereditary neuropathies; post-polio muscle dysfunction.

Erscheint lt. Verlag	30.3.1998
Zusatzinfo	illustrations
Verlagsort	Chichester
Sprache	englisch
Maße	153 x 234 mm
Gewicht	1050 g
Einbandart	gebunden
Themenwelt	Medizinische Fachgebiete ► Innere Medizin ► Rheumatologie
	Medizin / Pharmazie ► Medizinische Fachgebiete ► Neurologie
	Studium ► 2. Studienabschnitt (Klinik) ► Humangenetik
	Naturwissenschaften ► Biologie ► Humanbiologie
ISBN-10	0-471-97817-5 / 0471978175
ISBN-13	978-0-471-97817-6 / 9780471978176
Zustand	Neuware