PRISMA checklist, protocol, search term, meta-analyses on outcomes other than primary, and characteristics of excluded studies. (PDF 1341 kb
Duchenne muscular dystrophy is caused by mutations in the DMD gene that disrupt the open reading fra...
In Duchenne muscular dystrophy (DMD), the reading frame of an out-of-frame DMD deletion can be repai...
INTRODUCTION: The aim of this international collaborative effort was to report 36-month longitudina...
Table S1. Oligonucleotide Sequences of 15 multiplex PCR sets and amplification size fragments. (DOCX...
Importance: In Duchenne muscular dystrophy (DMD), the reading frame of an out-of-frame DMD deletion ...
Duchenne muscular dystrophy (DMD) is a severe, pro-gressive muscle-wasting disorder, while Becker mu...
Background: Eteplirsen, the first FDA-approved RNA-modifying therapy for DMD, is applicable to ∼13% ...
Duchenne muscular dystrophy (DMD), the most common and serious form of childhood muscle wasting is g...
IMPORTANCE: In Duchenne muscular dystrophy (DMD), the reading frame of an out-of-frame DMD deleti...
Antisense oligonucleotide (AON)-mediated exon skipping is an emerging therapeutic for individuals wi...
Clinical characteristics and WES results (including evidence of pathogenicity according to ACMG crit...
International audienceBackground Duchenne muscular dystrophy is a lethal disease caused by lack of d...
Dystrophin rescue is not preferential to a particular myofiber type. IF in serial sections were stai...
Maximum trunk angles. Median and interquartile ranges for maximum trunk angles during active trunk m...
Lists of rare (< 1%) variants in genes related with “muscle phenotype” for individual patients. (XLS...
Duchenne muscular dystrophy is caused by mutations in the DMD gene that disrupt the open reading fra...
In Duchenne muscular dystrophy (DMD), the reading frame of an out-of-frame DMD deletion can be repai...
INTRODUCTION: The aim of this international collaborative effort was to report 36-month longitudina...
Table S1. Oligonucleotide Sequences of 15 multiplex PCR sets and amplification size fragments. (DOCX...
Importance: In Duchenne muscular dystrophy (DMD), the reading frame of an out-of-frame DMD deletion ...
Duchenne muscular dystrophy (DMD) is a severe, pro-gressive muscle-wasting disorder, while Becker mu...
Background: Eteplirsen, the first FDA-approved RNA-modifying therapy for DMD, is applicable to ∼13% ...
Duchenne muscular dystrophy (DMD), the most common and serious form of childhood muscle wasting is g...
IMPORTANCE: In Duchenne muscular dystrophy (DMD), the reading frame of an out-of-frame DMD deleti...
Antisense oligonucleotide (AON)-mediated exon skipping is an emerging therapeutic for individuals wi...
Clinical characteristics and WES results (including evidence of pathogenicity according to ACMG crit...
International audienceBackground Duchenne muscular dystrophy is a lethal disease caused by lack of d...
Dystrophin rescue is not preferential to a particular myofiber type. IF in serial sections were stai...
Maximum trunk angles. Median and interquartile ranges for maximum trunk angles during active trunk m...
Lists of rare (< 1%) variants in genes related with “muscle phenotype” for individual patients. (XLS...
Duchenne muscular dystrophy is caused by mutations in the DMD gene that disrupt the open reading fra...
In Duchenne muscular dystrophy (DMD), the reading frame of an out-of-frame DMD deletion can be repai...
INTRODUCTION: The aim of this international collaborative effort was to report 36-month longitudina...
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