Quantitative NMRI and NMRS identify augmented disease progression after loss of ambulation in forearms of boys with Duchenne muscular dystrophy-Reference-Cited by-同舟云学术

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Quantitative NMRI and NMRS identify augmented disease progression after loss of ambulation in forearms of boys with Duchenne muscular dystrophy

Published:2015-07-27 Issue:9 Volume:28 Page:1150-1162
ISSN:0952-3480
Container-title:NMR in Biomedicine
language:en
Short-container-title:NMR Biomed.

Author:

Wary Claire¹²³,Azzabou Noura¹²³,Giraudeau Céline¹²³,Le Louër Julien¹²³,Montus Marie⁴,Voit Thomas⁵,Servais Laurent⁶,Carlier Pierre¹²³

Affiliation:

1. AIM-CEA, Institute of Myology; NMR Laboratory; Paris France

2. CEA, I BM, MIRCen; IdM NMR Laboratory; Paris France

3. UPMC University; Paris 06; Paris France

4. Généthon; Evry France

5. Institute of Myology; UPMC-INSERM U974, CNRS FRE 3617; Paris France

6. Institute of Myology; Clinical Trial and Database Unit; Paris France

Funder

ADNA, Advanced diagnostics for New therapeutical Approaches

Publisher

Wiley

Subject

Spectroscopy,Radiology Nuclear Medicine and imaging,Molecular Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/nbm.3352/fullpdf

Reference68 articles.

1. A systematic review and meta-analysis on the epidemiology of Duchenne and Becker muscular dystrophy;Mah;Neuromuscul. Disord.,2014

2. Overview on DMD exon skipping;Aartsma-Rus;Methods Mol. Biol.,2012

3. Emerging genetic therapies to treat Duchenne muscular dystrophy;Nelson;Curr. Opin. Neurol.,2009

4. Dystrophin and mutations: one gene, several proteins, multiple phenotypes;Muntoni;Lancet Neurol.,2003

5. Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study;Cirak;Lancet,2011

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