Duchenne Regulatory Science Consortium Meeting on Disease Progression Modeling for Duchenne Muscular Dystrophy

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Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management.

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Duchenne Regulatory Science Consortium Meeting on Disease Progression Modeling for Duchenne Muscular Dystrophy

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

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2017年學術文章

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2017年學術文章

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2017年學術文章

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name

Duchenne Regulatory Science Co ...... or Duchenne Muscular Dystrophy

@ast

Duchenne Regulatory Science Co ...... or Duchenne Muscular Dystrophy

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type

Item

label

Duchenne Regulatory Science Co ...... or Duchenne Muscular Dystrophy

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Duchenne Regulatory Science Co ...... or Duchenne Muscular Dystrophy

@en

prefLabel

Duchenne Regulatory Science Co ...... or Duchenne Muscular Dystrophy

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Duchenne Regulatory Science Co ...... or Duchenne Muscular Dystrophy

@en

P1476

Duchenne Regulatory Science Co ...... or Duchenne Muscular Dystrophy

@en

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Abby Bronson

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Brenda Wong

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Charles Lynn

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Craig M McDonald

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Dana Martin

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Elizabeth Habeeb-Louks

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Enrique Aviles

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Erik Henricson

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Glen Nuckolls

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Glenn Walter

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Skeletal muscles of ambulant children with Duchenne muscular dystrophy: validation of multicenter study of evaluation with MR imaging and MR spectroscopy.

The cooperative international neuromuscular research group Duchenne natural history study: glucocorticoid treatment preserves clinically meaningful functional milestones and reduces rate of disease progression as measured by manual muscle testing an

The cooperative international neuromuscular research group Duchenne natural history study--a longitudinal investigation in the era of glucocorticoid therapy: design of protocol and the methods used.

Magnetic resonance imaging and spectroscopy assessment of lower extremity skeletal muscles in boys with Duchenne muscular dystrophy: a multicenter cross sectional study

The 6-Minute Walk Test and Person-Reported Outcomes in Boys with Duchenne Muscular Dystrophy and Typically Developing Controls: Longitudinal Comparisons and Clinically-Meaningful Changes Over One Year.

Magnetic Resonance Assessment of Hypertrophic and Pseudo-Hypertrophic Changes in Lower Leg Muscles of Boys with Duchenne Muscular Dystrophy and Their Relationship to Functional Measurements.

Prevalence of Duchenne and Becker muscular dystrophies in the United States.

Multicenter prospective longitudinal study of magnetic resonance biomarkers in a large duchenne muscular dystrophy cohort.

The 6-minute walk test and other endpoints in Duchenne muscular dystrophy: longitudinal natural history observations over 48 weeks from a multicenter study

Reliability of the North Star Ambulatory Assessment in a multicentric setting.

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scholarly article

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10.1371/CURRENTS.MD.83071BBD728982F2F1073F4950E03586

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http://www.w3.org/2001/XMLSchema#string

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Richard T Abresch

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2017-01-12T00:00:00Z

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28228973

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P932

5300692

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Duchenne Regulatory Science Consortium Meeting on Disease Progression Modeling for Duchenne Muscular Dystrophy

about

P2860

P2860

Duchenne Regulatory Science Consortium Meeting on Disease Progression Modeling for Duchenne Muscular Dystrophy

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P31

P356

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P31

P356

P478

P50

P577

P698

P932