Clinical companion to the Molecular and genetic basis of neurological disease
著者
書誌事項
Clinical companion to the Molecular and genetic basis of neurological disease
Butterworth-Heinemann, c1998
2nd ed
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内容説明・目次
内容説明
This portable reference will enable physicians to quickly retrieve the information they need to assist in the diagnosis and treatment. Formatted for maximum accessibility, the "Clinical Companion" includes generous tables and lists. "The Molecular and Genetic Basis of Neurological Disease" is regarded as the most authoritative book of the basic neuroscience involving molecular science and molecular genetics for neurologists treating patients with genetic neurologic diseases. Readers of the "Clinical Companion" will benefit from the expertise of the main text without having to sift through the basic science in order to extract the material needed for a particular patient.
目次
- Molecular Genetics and Neurologic Disease: An Introduction
- Chromosome Disorders
- Prions
- Mitochondrial Disorders
- Peroxisomal Disorders
- Lysosomal Disorders
- Degenerative Disorders
- Multiple Sclerosis
- Neuro-oncology
- Ion Channel Disorders
- The Genetic Epilepsies
- Neuropathies and Neuronopathies
- Muscle Disorders
- The Phakomatoses: Disorders of Skin and Brain
- Lipoprotein Disorders
- Carbohydrate Disorders
- Amino Acid Disorders
- Purines
- The Porphyrias
- Metal Metabolism
- Vitamins
- The Genetics of Bipolar Disorder and Schizophrenia
- Gene Therapy and the Human Genome
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