Can outcomes in Duchenne muscular dystrophy be improved by public reporting of data? - Wikidata - awgldk - TriplyDB

Can outcomes in Duchenne muscular dystrophy be improved by public reporting of data?

Can outcomes in Duchenne muscular dystrophy be improved by public reporting of data?

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What can Duchenne Connect teach us about treating Duchenne muscular dystrophy?Dystrophin hydrophobic regions in the pathogenesis of Duchenne and Becker muscular dystrophies.Contemporary cardiac issues in Duchenne muscular dystrophy. Working Group of the National Heart, Lung, and Blood Institute in collaboration with Parent Project Muscular Dystrophy.The TREAT-NMD care and trial site registry: an online registry to facilitate clinical research for neuromuscular diseases Myositis registries and biorepositories: powerful tools to advance clinical, epidemiologic and pathogenic research.Corticosteroids in Duchenne muscular dystrophy: major variations in practice.Cystic fibrosis newborn screening: a model for neuromuscular disease screening?The TREAT-NMD Duchenne muscular dystrophy registries: conception, design, and utilization by industry and academia.Newborn screening for Duchenne muscular dystrophy in China: follow-up diagnosis and subsequent treatment.Clinical Follow-Up for Duchenne Muscular Dystrophy Newborn Screening: A Proposal.China's shift from population control to population quality: Implications for neurology.

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Can outcomes in Duchenne muscular dystrophy be improved by public reporting of data?

http://www.wikidata.org/entity/Q30000808

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2013 nî lūn-bûn

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2013 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2013 թվականի փետրվարին հրատարակված գիտական հոդված

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2013年の論文

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Can outcomes in Duchenne muscular dystrophy be improved by public reporting of data?

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Can outcomes in Duchenne muscular dystrophy be improved by public reporting of data?

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Can outcomes in Duchenne muscular dystrophy be improved by public reporting of data?

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Can outcomes in Duchenne muscular dystrophy be improved by public reporting of data?

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P2860

Glucocorticoid corticosteroids for Duchenne muscular dystrophy

Collaborating to bring new therapies to the patient--the TREAT-NMD model.

If you build a rare disease registry, will they enroll and will they use it? Methods and data from the National Registry of Myotonic Dystrophy (DM) and Facioscapulohumeral Muscular Dystrophy (FSHD).

DuchenneConnect Registry Report.

Practice parameter: corticosteroid treatment of Duchenne dystrophy: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.

Improving subspecialty healthcare: lessons from cystic fibrosis.

Widening gap in age at muscular dystrophy-associated death between blacks and whites, 1986-2005

The muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): surveillance methodology.

Managing Duchenne muscular dystrophy--the additive effect of spinal surgery and home nocturnal ventilation in improving survival.

Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): case definition in surveillance for childhood-onset Duchenne/Becker muscular dystrophy.

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