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 …
physical function in older adults. There is an increasing amount of research to support the …
Quantitative proton MR techniques for measuring fat
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 …
distributions are important tools in physiology research. They are critically needed in studies …
Measurement of intramuscular fat by muscle echo intensity
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 …
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 …
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 …
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 …
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
Facioscapulohumeral muscular dystrophy (FSHD) is an untreatable disease, characterized
by asymmetric progressive weakness of skeletal muscle with fatty infiltration. Although the …
by asymmetric progressive weakness of skeletal muscle with fatty infiltration. Although the …
Cardiac Phenotypes in Hereditary Muscle Disorders: JACC State-of-the-Art Review
Hereditary muscular diseases commonly involve the heart. Cardiac manifestations
encompass a spectrum of phenotypes, including both cardiomyopathies and rhythm …
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 …
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 …
characterized by severe muscle hypotonia at birth, progressive scoliosis, joint hypermobility …