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CME Activity

Neurology: Volume 77, Number 22, November 29, 2011

Faculty

Yusuf A. Rajabally, MD, FRCP

Department of Neurology
University Hospitals of Leicester
Leicester, UK

Jean Martey, BSc

Department of Neurology
University Hospitals of Leicester
Leicester, UK

E. Matthews, MRCP

MRC Centre for Neuromuscular Disease
UCL Institute of Neurology
London, UK

S. Portaro, MD

MRC Centre for Neuromuscular Disease
UCL Institute of Neurology
London, UK
Department of Neurosciences
Psychiatry and Anaesthesiology
University of Messina
AOU Policlinico “G. Martino”
Messina, Italy

Q. Ke, MD

Department of Neurology
The First Affiliated Hospital of College of Medicine
Zhejiang University
Hangzhou, China
Department of Neurology
University of Rochester
Rochester, NY

R. Sud, PhD

Neurogenetics Unit
National Hospital for Neurology and Neurosurgery
London, UK

A. Haworth, MSc

Neurogenetics Unit
National Hospital for Neurology and Neurosurgery
London, UK

M.B. Davis, PhD

Neurogenetics Unit
National Hospital for Neurology and Neurosurgery
London, UK

R.C. Griggs, MD

Department of Neurology
University of Rochester
Rochester, NY

M.G. Hanna, FRCP

MRC Centre for Neuromuscular Disease
UCL Institute of Neurology
London, UK

Accredited by

American Academy of Neurology

Course Description

Upon completion of the article by Rajabally and Martey, the participant should be able to:
• State how much more likely neuropathy was found in patients with Parkinson disease (PD) as compared to patients with other neurologic conditions in this study
• Discuss the role of vitamin B12 deficiency in causing neuropathy in PD patients
• Discuss clinical factors which may be related to the development of neuropathy in PD patients


Upon completion of the article by Matthews et al, the participant should be able to:
• State the approximate percentage of cases of hypokalemic periodic paralysis (hypoPP) caused by CACNA1S or SCN4A mutations
• Describe the effect of genotype on the probability of response to acetazolamide in patients with hypoPP
• Discuss possible pathophysiological mechanisms underlying different known mutations

Activity Details

Credit Types:CME
Credit Amount:1.5 Credits
Release Date:2011-Nov-29
Expiration Date:2012-Nov-29
Registration Required:Yes
Cost:$624/yr
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