Muscle MRI in patients with dysferlinopathy: pattern recognition and implications for clinical trials

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Muscle MRI in patients with dysferlinopathy: pattern recognition and implications for clinical trials

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im Oktober 2018 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

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наукова стаття, опублікована в жовтні 2018

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Muscle MRI in patients with dy ...... plications for clinical trials

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Muscle MRI in patients with dy ...... plications for clinical trials

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Muscle MRI in patients with dy ...... plications for clinical trials

@en

Muscle MRI in patients with dy ...... plications for clinical trials

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Muscle MRI in patients with dy ...... plications for clinical trials

@en

Muscle MRI in patients with dy ...... plications for clinical trials

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P1476

Muscle MRI in patients with dy ...... plications for clinical trials

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P2093

Alan Pestronk

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Alessandro Rampado

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Andrew M Blamire

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Anna Mayhew

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Anne Marie Sawyer

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Anthony Peduto

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Bruce Harwick

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Carolina Tesi Rocha

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Claudio Semplicini

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David Bendahan

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P2860

Distal anterior compartment myopathy: a dysferlin mutation causing a new muscular dystrophy phenotype

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Comparing clinical data and muscle imaging of DYSF and ANO5 related muscular dystrophies.

Quantitative Skeletal Muscle MRI: Part 2, MR Spectroscopy and T2 Relaxation Time Mapping-Comparison Between Boys With Duchenne Muscular Dystrophy and Healthy Boys.

MRI biomarker assessment of neuromuscular disease progression: a prospective observational cohort study.

Magnetic resonance imaging of skeletal muscle disease.

Neuromuscular imaging in inherited muscle diseases

Examination of effects of corticosteroids on skeletal muscles of boys with DMD using MRI and MRS.

Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypes.

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1071-1081

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scholarly article

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10.1136/JNNP-2017-317488

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English

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Luca Bello

C Paradas

Volker Straub

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2018-10-01T00:00:00Z

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29735511

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6166612

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