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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...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Rouleau, Guy, Gaspar, Claudia, Ph. D.
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Amsterdam ; Boston : Academic Press, �2008.
Colección:Advances in genetics ; v. 63.
Temas:
Acceso en línea:Texto completo

MARC

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245 0 0 |a Advances in genetics  |n Volume 63,  |p Ion channel diseases /  |c edited by Guy Rouleau, Claudia Gaspar. 
246 3 |a Ion channel diseases 
260 |a Amsterdam ;  |a Boston :  |b Academic Press,  |c �2008. 
300 |a 1 online resource (x, 157 pages) :  |b illustrations. 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
490 1 |a Advances in genetics ;  |v v. 63 
504 |a Includes bibliographical references and index. 
588 0 |a Print version record. 
520 |a 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 component. This volume presents a broad and comprehensive overview of the inherited channelopathies in humans, including clinical, genetic and molecular aspects of these conditions, as well as novel genomic and modeling research approaches. Also included is a review of potential therapeutic approaches for each of these conditions. 
505 0 |a 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 
505 8 |a 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 
546 |a English. 
650 0 |a Ion channels. 
650 0 |a Membrane disorders. 
650 2 |a Ion Channels  |0 (DNLM)D007473 
650 6 |a Canaux ioniques.  |0 (CaQQLa)201-0145111 
650 6 |a Membranes (Biologie)  |x Maladies.  |0 (CaQQLa)201-0225750 
650 7 |a Ion channels  |2 fast  |0 (OCoLC)fst00978573 
650 7 |a Membrane disorders  |2 fast  |0 (OCoLC)fst01015838 
700 1 |a Rouleau, Guy. 
700 1 |a Gaspar, Claudia,  |c Ph. D. 
776 |z 0-12-374527-6 
830 0 |a Advances in genetics ;  |v v. 63. 
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