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Treatment for Charcot-Marie-Tooth disease

Published:2008-01-23 Issue: Volume: Page:
ISSN:1465-1858
Container-title:Cochrane Database of Systematic Reviews
language:en
Short-container-title:

Author:

Young Peter¹,De Jonghe Peter²,Stögbauer Florian³,Butterfass-Bahloul Trude⁴

Affiliation:

1. University of Münster ; Department of Neurology; Albert-Schweitzer-Str.33 Münster Germany 48129

2. University of Antwerp - CDE; VIB - Department of Molecular Genetics, Neurogenetics Group; Universiteitsplein 1 Antwerpen Belgium BE-2610

3. Klinikum Osnabruck; Department of Neurology; Am Finkenhugel 1 Osnabruck Germany 49076

4. University of Münster; Co-ordinating Centre for Clinical Trials (KKS); Von-Esmarch-Str. 62 Münster Germany 48129

Publisher

Wiley

Subject

Pharmacology (medical)

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/14651858.CD006052.pub2/fullpdf

Reference88 articles.

1. Double-blind controlled trials of Cronassial in chronic neuromuscular diseases and ataxia;Bradley;Neurology,1988

2. Effective orthotic therapy for the painful cavus foot: a randomized controlled trial;Burns;Journal of the American Podiatric Medical Association,2006

3. Resistance training exercise and creatine in patients with Charcot-Marie-Tooth disease;Chetlin;Muscle & Nerve,2004

4. Creatine monohydrate does not increase strength in patients with hereditary neuropathy;Doherty;Neurology,2001

5. Strength training in patients with myotonic dystrophy and hereditary motor and sensory neuropathy: a randomized clinical trial;Lindeman;Archives of Physical and Medical Rehabilitation,1995

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1. Identification of biallelic mutations in MCM3AP and comprehensive literature analysis;Frontiers in Genetics;2024-08-20

2. Acute neurologic deterioration in a patient with asymptomatic Charcot-Marie-Tooth disease following three doses of Brentuximab-Vedotin;Leukemia & Lymphoma;2024-06-03

3. Bilateral hearing impairment as an early symptom in a patient with Charcot-Marie-Tooth Type 1: the first case report from Syria;Annals of Medicine & Surgery;2024-03-19

4. Case report: A novel variant (H49N) in Myelin Protein Zero gene is responsible for a patient with Charcot–Marie–Tooth disease;Frontiers in Neurology;2024-02-28

5. Rehabilitation bei neuromuskulären Erkrankungen;NeuroRehabilitation;2024

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