Literature DB >> 397411

Lack of benefit of allopurinol in Duchenne dystrophy.

J R Mendell, D O Wiechers.   

Abstract

A double-bline, controlled study was conducted to assess the effects of allopurinol on Duchenne muscular dystrophy. Six patients--three treated with allopurinol and three given a placebo--were followed up for one year and were evaluated by functional and manual muscle testing as well as by determination of serum creatine kinase (CK) levels. Patients in both the allopurinol-treated group and the placebo group deteriorated at varying rates without evidence of therapeutic benefit. To exclude the possibility of error attributable to small sample size, all six patients were treated with allopurinol for an additional eight-week period. Muscle strength continued to deteriorate during this phase of the study.

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Year:  1979        PMID: 397411     DOI: 10.1002/mus.880020108

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  6 in total

1.  Increased catalase expression improves muscle function in mdx mice.

Authors:  Joshua T Selsby
Journal:  Exp Physiol       Date:  2010-11-01       Impact factor: 2.969

2.  Metabolite profiling of human muscle extracts by isotachophoresis.

Authors:  F Oerlemans; C van Bennekom; C De Bruyn; S Kulakowski
Journal:  J Inherit Metab Dis       Date:  1981       Impact factor: 4.982

Review 3.  Antioxidants to prevent respiratory decline in people with Duchenne muscular dystrophy and progressive respiratory decline.

Authors:  Luis Garegnani; Martin Hyland; Pablo Roson Rodriguez; Camila Micaela E Escobar Liquitay; Juan Va Franco
Journal:  Cochrane Database Syst Rev       Date:  2021-11-08

Review 4.  Antioxidants to prevent respiratory decline in people with Duchenne muscular dystrophy and progressive respiratory decline.

Authors:  Luis Garegnani; Martin Hyland; Pablo Roson Rodriguez; Camila Micaela Escobar Liquitay; Juan Va Franco
Journal:  Cochrane Database Syst Rev       Date:  2021-12-01

5.  Functional evaluation of Duchenne muscular dystrophy: proposal for a protocol.

Authors:  F Cornelio; F Dworzak; L Morandi; E Fedrizzi; M R Balestrini; L Gondoni
Journal:  Ital J Neurol Sci       Date:  1982-12

Review 6.  Metabogenic and Nutriceutical Approaches to Address Energy Dysregulation and Skeletal Muscle Wasting in Duchenne Muscular Dystrophy.

Authors:  Emma Rybalka; Cara A Timpani; Christos G Stathis; Alan Hayes; Matthew B Cooke
Journal:  Nutrients       Date:  2015-11-26       Impact factor: 5.717

  6 in total

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