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Neurologic Channelopathies

  • 1st Edition, Volume 203 - August 20, 2024
  • Latest edition
  • Editor: Michael G. Hanna
  • Language: English

Neurological Channelopathies, Volume 203 begins with an introductory overview highlighting common mechanistic themes that cut across different CNS and PNS presentations, but that a… Read more

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Description

Neurological Channelopathies, Volume 203 begins with an introductory overview highlighting common mechanistic themes that cut across different CNS and PNS presentations, but that also have potential for common treatment approaches, considering classification, genetics, and fundamental physiology of ion channels. Subsequent chapters present a detailed consideration of all genetic and immunological channelopathies. Each chapter considers Pathophysiological underpinnings - genetic or immunological; Clinical presentations; Diagnostic approach; and Treatment and management.

In the last 15 years, a combination of detailed clinical, genetic, molecular electrophysiological, and immunological research has combined to result in a deep understanding of a subgroup of neurological diseases spanning the central and peripheral nervous system and which have become known collectively as the Neurological Channelopathies. Although it was originally considered that significant ion channel dysfunction would not be compatible with life, we now know this is often not the case, although severe disease can often be the result. Given these major advances, it is now the right time to combine this knowledge into a single HCN volume dedicated to the topics at hand.

Key features

  • Identifies importance of ion channels to CNS & PNS function
  • Considers the classification, genetics, and physiology of ion channels
  • Presents all major immunological and genetic channelopathies
  • Provides clinical presentation, diagnosis, and treatment of channelopathies

Readership

Clinical neurologists

Table of contents

1. Structure-function and pharmacological aspects of ion channels relevant to neurologic channelopathies

2. Inherited Myotonias

3. Periodic Paralysis 

4. Andersen-Tawil syndrome

5. Congenital myasthenic syndromes

6. Human pain channelopathies

7. Pediatric Neuromuscular Channelopathies

8. The Episodic Ataxias

9. Familial Hemiplegic Migraine

10. Paroxysmal Movement Disorders

11. Epilepsies

12. Myasthenia Gravis

13. Neuromyotonia

14. Stiff person Syndrome

15. Autoantibody-mediated central nervous system channelopathies

Product details

  • Edition: 1
  • Latest edition
  • Volume: 203
  • Published: August 20, 2024
  • Language: English

About the editor

MH

Michael G. Hanna

Michael G Hanna is Director of the UCL Institute of Neurology, University College London and professor in clinical neurology and consultant neurologist at the National Hospital for Neurology and Neurosurgery, Queen Square, London, and also Director of the Medical Research Council (MRC) Centre for Neuromuscular Disease. He has published over 100 peer-reviewed papers in neurology, authored 15 book chapters and one book in clinical neurology. He serves as editor of the journal of Neurology, Neurosurgery, and Psychiatry.and is co-author of the textbook Tutorials in Differential Diagnosis, 4e.
Affiliations and expertise
Director, UCL Institute of Neurology, University of College London, London, UK; Professor in Clinical Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK; Consultant Neurologist, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK; Director, Medical Research Council (MRC) Centre for Neuromuscular Disease, London, UK

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