Oakstone Electrodiagnostic Medicine and Neuromuscular Disorders 2023

40 $

+ Include: 41 videos + 2 pdfs, size: 6.39 GB

+ Target Audience: neurologists, physiatrists physical medicine & rehabilitation (PM&R) doctors, neurology residents and fellows, PM&R residents and fellows

Description

+ Include: 41 videos + 2 pdfs, size: 6.39 GB

+ Target Audience: neurologists, physiatrists physical medicine & rehabilitation (PM&R) doctors, neurology residents and fellows, PM&R residents and fellows

+ Sample video: contact me for sample video

+ Information:

Convenient, Comprehensive Neurology and PM&R CME

Designed for neurologists and physical medicine & rehabilitation doctors, residents, and fellows, this continuing medical education program covers all diagnostic and management approaches to both inherited and acquired neuromuscular conditions.

The 41 lectures in Electrodiagnostic Medicine and Neuromuscular Disorders — each just 30 and 45 minutes in length — delve into basic techniques and clinical applications of electrodiagnosis and ultrasound, as well as generalized disorders, motor neuron diseases, polyneuropathies, neuromuscular junction disorders, and myopathies. Key take-home points from this online CME program include:

  • Basics of Needle EMG: Voluntary Activity. Motor unit potential waveform reflects the change in motor unit architecture due to disease processes, while the interference pattern provides information about the number of motor units and their activation.
  • Neuropathies Associated with Systemic Disease and Cancer. Countless systemic disorders — metabolic, nutritional, inflammatory, infectious, neoplastic, and others — can cause neuropathy and accordingly, neuropathy can take many forms. Carefully characterizing the phenotype of neuropathy can help narrow down the relevant causes.
  • Muscle Channelopathies. For a patient with a personal and family history of muscle stiffness and pain, consider genetic testing for myotonic disorders.
  • And more…

Date of Original Release: February 15, 2023
Date Credits Expire: February 15, 2026

Learning Objectives

At the completion of this course, you should be able to:

  • List the methods of rehabilitation management of neuromuscular disease
  • Recognize the common neuromuscular mimics of the upper extremity
  • Identify the signs of neuropathies found on physical examination
  • List the substances that can cause toxic polyneuropathies
  • Compare the two groups of disorders found in muscle channelopathies
  • Describe the classic presentation of amyotrophic lateral sclerosis
  • Explain how to tailor the treatment of myasthenia gravis to disease severity and individual patient
  • Discuss how to evaluate a patient with generalized weakness
  • Outline the role of electromyography in focal mononeuropathies of the leg
  • Name the common inherited and acquired causes of rhabdomyolysis

Intended Audience

This educational activity was designed for neurologists, physiatrists physical medicine & rehabilitation (PM&R) doctors, neurology residents and fellows, PM&R residents and fellows.

 

 

+ Topics:

1. Basics of Nerve Conduction Studies – Sensory.mp4
2. Basics of Nerve Conduction Studies – Motor.mp4
3. EMG – Spontaneous Activity.mp4
4. Basics of Needle EMG – Voluntary Activity.mp4
5. Assessment of the Neuromuscular Junction – Repetitive Stimulation & Single Fiber EMG.mp4
6. Autonomic Function Testing.mp4
7. Electrodiagnosis of Focal Upper Extremity Mononeuropathies.mp4
8. Electrophysiologic Approach to Brachial Plexopathies.mp4
9. Focal Mononeuropathies in the Leg.mp4
10. Electrodiagnostic Approach to Lower Limb Radiculopathy & Plexopathy.mp4
11. Peripheral Nerve Ultrasound.mp4
12. Approach to the Patient with Generalized Weakness.mp4
13. Approach to the Patient with Multifocal Weakness.mp4
14. Approach to the Patient with Scapular Winging.mp4
15. Approach to the Patient with Diplopia.mp4
16. Approach to the Patient with Facial Weakness.mp4
17. Approach to the Patient with Clinical Myotonia.mp4
18. Approach to the Patient with Cramps.mp4
19. Amyotrophic Lateral Sclerosis.mp4
20. Atypical Motor Neuron Diseases.mp4
21. Spinal Muscular Atrophy.mp4
22. Approach to Neuropathies.mp4
23. Charcot-Marie-Tooth (CMT) & Related Disorders.mp4
24. Guillain-Barre & Other Acute Acquired Neuropathies.mp4
25. Chronic Inflammatory Demyelinating Polyneuropathy & Related Disorders.mp4
26. Neuropathies Associated with Systemic Disease & Cancer.mp4
27. Toxic Polyneuropathies.mp4
28. Myasthenia Gravis.mp4
29. Congenital, Lambert-Eaton Myasthenic Syndrome, Botulism.mp4
30. Clinical Approach to Muscle Disease.mp4
31. Muscular Dystrophies.mp4
32. Congenital Myopathies.mp4
33. Metabolic Myopathies.mp4
34. Mitochondrial Myopathies.mp4
35. Muscle Channelopathies.mp4
36. Idiopathic Inflammatory Myopathies.mp4
37. Systemic & Toxic Myopathies.mp4
38. Approach to the Patient with Rhabdomyolysis.mp4
39. Neonatal Hypotonia – Approach to the Floppy Infant.mp4
40. Neuromuscular Mimics.mp4
41. Rehabilitation of Neuromuscular Disorders.mp4
Questions.pdf
Syllabus.pdf

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