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Advances in genetics Volume 63, Ion channel diseases /
Ion channel dysfunction in humans leads to impairment of the excitable processes necessary for the normal function of several tissues, such as muscle and brain. It follows that an increasing number of human diseases have been associated with malfunctioning ion channels, many of which have a genetic...
| Clasificación: | Libro Electrónico |
|---|---|
| Otros Autores: | , |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Amsterdam ; Boston :
Academic Press,
�2008.
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| Colección: | Advances in genetics ;
v. 63. |
| Temas: | |
| Acceso en línea: | Texto completo |
Tabla de Contenidos:
- Front Cover; Ion Channel Diseases; Copyright Page; Contents; Contributors; Part I: Muscle Channelopathies; Chapter 1: Periodic Paralysis; I. Introduction; III. Hyperkalemic Periodic Paralysis; IV. Other Types of Periodic Paralysis; VI. Treatment and Care of hypoPP Patients; VII. Conclusion; Acknowledgments; I. Introduction; V. Myotonia Congenita in Animal Models; Acknowledgments; References; Chapter 3: Familial Hemiplegic Migraine; II. The Migraine Attack: Clinical Phases and Pathophysiology; III. The Migraine Aura and Cortical Spreading Depression; IV. Migraine as a Genetic Disorder
- VI. Functional Consequences of FHM MutationsVIII. Concluding Remarks; Acknowledgments; Acknowledgments; Part II: Internal Diseases; Chapter 5: Channelopathies of Transepithelial Transport and Vesicular Function; I. Introduction; II. Disorders; III. Concluding Remarks; References; Index