Intermuscular fat: a review of the consequences and causes

O Addison, RL Marcus, PC LaStayo… - International journal of …, 2014 - Wiley Online Library
Muscle's structural composition is an important factor underlying muscle strength and
physical function in older adults. There is an increasing amount of research to support the …

Quantitative proton MR techniques for measuring fat

HH Hu, HE Kan - NMR in biomedicine, 2013 - Wiley Online Library
Accurate, precise and reliable techniques for the quantification of body and organ fat
distributions are important tools in physiology research. They are critically needed in studies …

Measurement of intramuscular fat by muscle echo intensity

HJ Young, NT Jenkins, Q Zhao, KK Mccully - Muscle & nerve, 2015 - Wiley Online Library
Introduction: The aim of this study was to compare ultrasound echo intensity (EI) with high‐
resolution T1‐weighted MRI and to establish calibration equations to estimate percent …

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

RJ Willcocks, WD Rooney, WT Triplett… - Annals of …, 2016 - Wiley Online Library
Objective The aim of this study was to describe Duchenne muscular dystrophy (DMD)
disease progression in the lower extremity muscles over 12 months using quantitative …

5′ UTR CGG repeat expansion in GIPC1 is associated with oculopharyngodistal myopathy

J Xi, X Wang, D Yue, T Dou, Q Wu, J Lu, Y Liu, W Yu… - Brain, 2021 - academic.oup.com
Oculopharyngodistal myopathy is a late-onset degenerative muscle disorder characterized
by ptosis and weakness of the facial, pharyngeal, and distal limb muscles. A recent report …

A population-based epidemiologic study of adult neuromuscular disease in the Republic of Ireland

S Lefter, O Hardiman, AM Ryan - Neurology, 2017 - AAN Enterprises
Objective: To estimate the prevalence rates (PRs) of acquired and inherited neuromuscular
diseases (NMD) in the adult Irish population, reflecting the burden of these conditions in a …

Distinct disease phases in muscles of facioscapulohumeral dystrophy patients identified by MR detected fat infiltration

BH Janssen, NBM Voet, CI Nabuurs, HE Kan… - PloS one, 2014 - journals.plos.org
Facioscapulohumeral muscular dystrophy (FSHD) is an untreatable disease, characterized
by asymmetric progressive weakness of skeletal muscle with fatty infiltration. Although the …

Cardiac Phenotypes in Hereditary Muscle Disorders: JACC State-of-the-Art Review

E Arbustini, A Di Toro, L Giuliani, V Favalli… - Journal of the American …, 2018 - jacc.org
Hereditary muscular diseases commonly involve the heart. Cardiac manifestations
encompass a spectrum of phenotypes, including both cardiomyopathies and rhythm …

Skeletal muscle quantitative nuclear magnetic resonance imaging follow-up of adult Pompe patients

PG Carlier, N Azzabou, PL de Sousa, A Hicks… - Journal of inherited …, 2015 - Springer
Adult late-onset Pompe disease is most often a slowly progressive limb-girdle and spine
extensor muscle dystrophy, due to defective lysosomal acid maltase. With the exception of …

Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss

M Baumann, C Giunta, B Krabichler… - The American Journal of …, 2012 - cell.com
We report on an autosomal-recessive variant of Ehlers-Danlos syndrome (EDS)
characterized by severe muscle hypotonia at birth, progressive scoliosis, joint hypermobility …