Standing at the forefront of neurogenetic medicine, this reference supplies the tools and information required by clinicians to become familiar with modern neurogenetic approaches and apply the data gleaned from these technologies to the diagnosis and treatment of neurogenetic disorders, as well as traditionally non-genetic conditions such as Parkinson's and Alzheimer's disease.

Produktinformation

Utgivningsdatum2005-11-01
Mått178 x 254 x undefined mm
Vikt1 542 g
FormatInbunden
SpråkEngelska
SerieNeurological Disease and Therapy
Antal sidor786
FörlagTaylor & Francis Inc
ISBN9780824729424

Tillhör följande kategorier

Medicinsk genetik inom Medicin
Biovetenskap inom Naturvetenskap och teknik
Neurologi och klinisk neurofysiologi inom Medicin

Overview. Modern Approaches to Neurogenetic Conditions. Genetic Testing. Genetic Couseling. Genomic Approaches and Medicine. Gene Therapy. Ethical Dilemmas. Neurogenetic Diseases. Inherited Neuropathies. Duchenne/Becker Muscular Dystrophy. Limb Girdle Muscular Dystrophy. Non-Dystrophic Disorders of Muscle. Myotonic Dystrophy. Spinal Muscular Atrophy. Hereditary Spastic Paraparesis. Mitochondrial Disorders. Friedreich Ataxia. Autosomal Dominant Ataxias. Huntington Disease. Wilson Disease. Dystonia and Other Inherited Movement Disorders. Inherited Dementias. Inherited Epilepsies. Leukodystrophies. Storage Diseases. Genetic Forms of Common Neurodegenerative Disease. Parkinson's Disease. Alzheimer's Disease. Tauopathies. Amyotrophic Lateral Scleosis. Prion Disease

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Produktinformation

Utgivningsdatum2005-11-01
Mått178 x 254 x undefined mm
Vikt1 542 g
FormatInbunden
SpråkEngelska
SerieNeurological Disease and Therapy
Antal sidor786
FörlagTaylor & Francis Inc
ISBN9780824729424

Tillhör följande kategorier

Medicinsk genetik inom Medicin
Biovetenskap inom Naturvetenskap och teknik
Neurologi och klinisk neurofysiologi inom Medicin

Overview. Modern Approaches to Neurogenetic Conditions. Genetic Testing. Genetic Couseling. Genomic Approaches and Medicine. Gene Therapy. Ethical Dilemmas. Neurogenetic Diseases. Inherited Neuropathies. Duchenne/Becker Muscular Dystrophy. Limb Girdle Muscular Dystrophy. Non-Dystrophic Disorders of Muscle. Myotonic Dystrophy. Spinal Muscular Atrophy. Hereditary Spastic Paraparesis. Mitochondrial Disorders. Friedreich Ataxia. Autosomal Dominant Ataxias. Huntington Disease. Wilson Disease. Dystonia and Other Inherited Movement Disorders. Inherited Dementias. Inherited Epilepsies. Leukodystrophies. Storage Diseases. Genetic Forms of Common Neurodegenerative Disease. Parkinson's Disease. Alzheimer's Disease. Tauopathies. Amyotrophic Lateral Scleosis. Prion Disease