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Channelopathies : common mechanisms in aura, arrhythmia, and alkalosis

Author: Karin Jurkat-Rott; Frank Lehmann-Horn
Publisher: Amsterdam ; New York : Elsevier, 2000.
Edition/Format:   eBook : Document : EnglishView all editions and formats
Summary:
This book describes human hereditary ion channel diseases of voltage- and ligand-gated ion channels covering the diverse fields of medicine myology, neurology, cardiology, and nephrology requiring a wide and interdisciplinary readership. Interesting parallels in pathogenetic mechanisms of disease are especially emphasized to interest even highly specialized readers in entities outside of their fields. Each author  Read more...
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Genre/Form: Electronic books
Additional Physical Format: Print version:
Channelopathies.
Amsterdam ; New York : Elsevier, 2000
(DLC) 2001265235
(OCoLC)45593097
Material Type: Document, Internet resource
Document Type: Internet Resource, Computer File
All Authors / Contributors: Karin Jurkat-Rott; Frank Lehmann-Horn
ISBN: 9780444504890 0444504893 0080528856 9780080528854 1281026247 9781281026248
OCLC Number: 162131172
Description: 1 online resource (xiv, 368 pages) : illustrations
Contents: Cover --
Contents --
Foreword --
Preface --
Introduction --
Part 1: Muscle diseases --
Chapter 1. Sodium and calcium channelopathies of sarcolemma: periodic paralyses, paramyotonia congenita and potassium-aggravated myotonia --
Chapter 2. Muscle chloride channelopathies: myotonia congenita --
Chapter 3. Molecular aspects of malignant hyperthermia and central core disease --
Chapter 4. Mutations affecting muscle nicotinic acetylcholine receptors and their role in congenital myasthenic syndromes --
Chapter 5. Ion channel defects in primary electrical diseases of the heart --
Part 2: Neuronal diseases --
Chapter 6. Migraine and ataxias --
Chapter 7. Genetic analysis of idiopathic epilepsies: the role of ion channel mutations --
Chapter 8. The inhibitory glycine receptor as a model of hereditary channelopathies --
Part 3: Internal diseases --
Chapter 9. Cystic fibrosis --
Chapter 10. Dent's disease: an hereditary nephrolithiasis caused by dysfunction of a voltage-gated chloride channel --
Chapter 11. Liddle's syndrome and pseudohypoaldosteronism type I --
Chapter 12. The role of ATP-sensitive K+ channels in familial hyperinsulinism --
Chapter 13. Hereditary hypokalemic salt-losing tubulopathies --
Overview --
Table of known channelopathies --
Subject Index --
Last Page.
Responsibility: [edited] by Frank Lehmann-Horn and Karin Jurkat-Rott.
More information:

Abstract:

Describes human hereditary ion channel diseases of voltage- and ligand-gated ion channels covering the diverse fields of medicine myology, neurology, cardiology, and nephrology requiring an  Read more...

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