Neuromuscular Pathology Made Easy

 
 
CRC Press
  • 1. Auflage
  • |
  • erscheint ca. am 10. Januar 2021
 
  • Buch
  • |
  • Hardcover
  • |
  • 240 Seiten
978-0-367-63427-8 (ISBN)
 
The scope of Neuromuscular Pathology continuous to expand, as evidenced by the numerous multivolume and speciality texts published in recent years. This short textbook provides a complete overview of both clinical and histological aspects of common and rare neuromuscular diseases. The objective is twofold: to provide information about neuromuscular diseases in a simplified, integrated, and rapidly accessible format suited to those initially encountering the discipline, and also to provide a clear approach using simple pictures, tables and algorithms to illustrate histological features in muscle and nerve biopsy.
This volume is conveniently divided into three sections with a total of 30 chapters. The first section deals with basic principles of neuromuscular histology and physiology, processing technique, histochemistry, and laboratory management. The second and third sections deal with neuromuscular diseases that are summarized in a stepwise approach, complemented by algorithms and organized tables.

A simplified, integrated, and rapidly accessible format covering both common and rare neuromuscular diseases

Clear simple illustrations, organized tables and algorithms to aid the reader in finding an easy approach to accurate diagnosis

Practical tips to facilitate histopathological diagnosis.

Clinical scenarios discussing common neuromuscular conditions
Neurologists, neuropathologists, trainees and medical students involved in clinical neuroscience and pathology will find this guide of practical benefit in both education and practice.
  • Englisch
  • London
  • |
  • Großbritannien
Taylor & Francis Ltd
  • Für höhere Schule und Studium
  • 37
  • |
  • 19 s/w Photographien bzw. Rasterbilder, 101 Farbfotos bzw. farbige Rasterbilder, 16 s/w Zeichnungen, 37 s/w Tabellen
  • |
  • 37 tables, 19 halftones, 101 color halftones and 16 line drawings
  • Höhe: 216 mm
  • |
  • Breite: 140 mm
978-0-367-63427-8 (9780367634278)
weitere Ausgaben werden ermittelt
Maher Kurdi, MD, FRCPC, EFN
Clinical Assistant Professor
Department of Pathology
Faculty of Medicine in Rabigh
King Abdulaziz University
Kingdom of Saudi Arabia
Section A General
Chapter 1: Muscle and Nerve Histology
1.1. Muscle histology
1.1.a Mitochondria
1.2. Peripheral nerve histology
Chapter 2: Muscle and Nerve Fibers Classification
2.1. Muscle fiber classification
2.2. Peripheral nerve classification
Chapter 3: Clinical Neurophysiology with Ahmed Abuzinadah
3.1. Nerve conduction study
3.2. Electromyography
Chapter 4: Neuromuscular Laboratory
Chapter 5: Chemical Materials Used in the Lab
Chapter 6: Biopsy Processing Protocol with Habib Bin Attiah
6.1. Muscle
6.2. Nerve
Chapter 7: Histochemistry Protocol with Fawaz Siddiq
7.1. Histochemical reaction
7.2. Histochemical methods
7.3. Immunohistochemistry
7.4. Histological artifacts
Chapter 8: Genetic Basis with Ashraf Dallol
8.1. Single or multiple gene approach
8.2. Whole exam and genome sequencing
8.3. RNA sequencing
Chapter 9: Neuromuscular Final Report
9.1. Muscle biopsy report template
9.2. Nerve biopsy report template
Section B Muscle
Chapter 10: Initial Approach in Muscle Biopsy
10.1. Myopathic features
10.2. Neuropathic features
10.3. Dystrophic features
Chapter 11: Differential Diagnosis
Chapter 12: Electron Microscopy
Chapter 13: Classification of Myopathy
Chapter 14: Approach to Neuromyopathy
14.1. Neuromyopathy with lack of inflammation
14.1.a. Paraneoplastic-induced neuromyopathy
14.1.b. Drug-induced neuromyopathy
14.2. Neuromyopathy with inflammation
Chapter 15: Approach to Vacuolar Myopathy
Chapter 16: Muscular Dystrophy Diseases
Chapter 17: Inherited Myopathic Diseases
Chapter 18: Non-Congenital Acquired Myopathies
18.1. Chronic diseases-induced myopathies
18.2. Toxic myopathies
18.2.a. Statin-induced myopathy
18.3. Critical care illness myopathy

Chapter 19: Metabolic Myopathies
19.1. Glycogen storage diseases
19.1.a. POMPE disease
19.2. Lipid storage diseases
19.3. Mitochondrial myopathies
19.4. Other metabolic myopathies
19.4.a. Amyloid myopathy
Chapter 20: Inflammatory Myopathies
20.1. Polymyositis
20.2. Dermatomyositis
20.3. Immune-Mediated Necrotizing Myopathies
20.4. Overlap myositis
20.5. Inclusion body myositis
20.6. Granulomatous myositis
20.7. Treated myositis in muscle biopsy
Chapter 21: Chronic Denervation Myopathies with Ahmed Bamaga
21.1. Chronic denervation atrophy
21.2. Spinal muscular atrophy
Chapter 22: Axial Myopathy
Chapter 23: Fasciitis
Section C Nerve
Chapter 24: Classification of Neuropathy
Chapter 25: Diagnostic Approach in Nerve Biopsy
Chapter 26: Axonal Neuropathy
Chapter 27: Demyelinating Neuropathy
Chapter 28: Cellular and Extracellular Abnormalities
Chapter 29: Inflammatory Demyelination
29.1. Acute Inflammatory Demyelinating Neuropathy
29.2. Chronic Inflammatory Demyelinating Neuropathy
Chapter 30: Other Common Peripheral Neuropathies
Appendix

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