Risk of fracture in patients with Charcot-Marie-Tooth disease

Author:

Pouwels Sander1,de Boer Anthonius1,Leufkens Hubert G.M.1,Weber Wim E.J.2,Cooper Cyrus345,de Vries Frank1367

Affiliation:

1. Utrecht Institute for Pharmaceutical Sciences; University of Utrecht; Universiteitsweg 99 3584 CG Utrecht The Netherlands

2. Department of Neurology Maastricht; University Medical Centre; Maastricht The Netherlands

3. MRC Lifecourse Epidemiology Unit; University of Southampton; Southampton UK

4. NIHR Nutrition Biomedical Research Centre; University of Southampton; Southampton UK

5. NIHR Musculoskeletal Biomedical Research Unit; University of Oxford; Oxford UK

6. Department of Clinical Pharmacy and Toxicology; Maastricht University Medical Centre; Maastricht The Netherlands

7. School CAPHRI; Maastricht University; Maastricht The Netherlands

Funder

European Calcified Tissue Society

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Reference25 articles.

1. Epidemiology of peripheral neuropathy;Martyn;J Neurol Neurosurg Psychiatry,1997

2. Diagnosis, natural history, and management of Charcot-Marie-Tooth disease;Pareyson;Lancet Neurol,2009

3. Treatment for Charcot-Marie-Tooth disease;Young;Cochrane Database Syst Rev,2008

4. Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients;Mersiyanova;Hum Mutat,2000

5. Neuroarthropathy in Charcot-Marie-Tooth disease;Bruckner;Ann Rheum Dis,1969

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