Serum Creatinine Distinguishes Duchenne Muscular Dystrophy from Becker Muscular Dystrophy in Patients Aged ≤3 Years: A Retrospective Study. - Wikidata - awgldk - TriplyDB

Serum Creatinine Distinguishes Duchenne Muscular Dystrophy from Becker Muscular Dystrophy in Patients Aged ≤3 Years: A Retrospective Study.

Serum Creatinine Distinguishes Duchenne Muscular Dystrophy from Becker Muscular Dystrophy in Patients Aged ≤3 Years: A Retrospective Study.

http://www.wikidata.org/entity/Q33646732

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Serum Creatinine Distinguishes Duchenne Muscular Dystrophy from Becker Muscular Dystrophy in Patients Aged ≤3 Years: A Retrospective Study.

http://www.wikidata.org/entity/Q33646732

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2017 nî lūn-bûn

@nan

2017 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2017 թվականի մայիսին հրատարակված գիտական հոդված

@hy

2017年の論文

@ja

2017年論文

@yue

2017年論文

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2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

name

Serum Creatinine Distinguishes ...... Years: A Retrospective Study.

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Serum Creatinine Distinguishes ...... Years: A Retrospective Study.

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type

label

Serum Creatinine Distinguishes ...... Years: A Retrospective Study.

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Serum Creatinine Distinguishes ...... Years: A Retrospective Study.

@en

prefLabel

Serum Creatinine Distinguishes ...... Years: A Retrospective Study.

@ast

Serum Creatinine Distinguishes ...... Years: A Retrospective Study.

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FNEUR.2017.00196

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Frontiers in Neurology

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Serum Creatinine Distinguishes ...... Years: A Retrospective Study.

@en

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Cheng Zhang

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

Huili Zhang

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

Jiqing Cao

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

Juan Yang

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

Liang Wang

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

Lulu Xiao

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

Menglong Chen

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

Ruojie He

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

Yiming Sun

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

P2860

Creatine and creatinine metabolism

DMD Mutations in 576 Dystrophinopathy Families: A Step Forward in Genotype-Phenotype Correlations

In utero fetal muscle biopsy: a precious aid for the prenatal diagnosis of Duchenne muscular dystrophy.

The metabolism of creatine-1-C14 by mice with hereditary muscular dystrophy

Optimizing exon skipping therapies for DMD.

Exon skipping restores dystrophin expression, but fails to prevent disease progression in later stage dystrophic dko mice

Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene.

A systematic review and meta-analysis on the epidemiology of Duchenne and Becker muscular dystrophy.

Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule.

MLPA-based genotype-phenotype analysis in 1053 Chinese patients with DMD/BMD.

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196

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10.3389/FNEUR.2017.00196

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8

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2017-05-08T00:00:00Z

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5421192

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