Comparison of dixon and T1-weighted MR methods to assess the degree of fat infiltration in duchenne muscular dystrophy patients.
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Chemical shift-based MRI to measure fat fractions in dystrophic skeletal muscle.Quantitative proton MR techniques for measuring fatHeterogeneity of muscle fat infiltration in children with spina bifida.In vitro and in vivo comparison of two-, three- and four-point Dixon techniques for clinical intramuscular fat quantification at 3 T.Muscle-fat MRI: 1.5 Tesla and 3.0 Tesla versus histology.Fat saturation in dynamic breast MRI at 3 Tesla: is the Dixon technique superior to spectral fat saturation? A visual grading characteristics study.Quantitative NMRI and NMRS identify augmented disease progression after loss of ambulation in forearms of boys with Duchenne muscular dystrophy.Muscle imaging data in late-onset Pompe disease reveal a correlation between the pre-existing degree of lipomatous muscle alterations and the efficacy of long-term enzyme replacement therapy.Quantifying disease activity in fatty-infiltrated skeletal muscle by IDEAL-CPMG in Duchenne muscular dystrophy.Skeletal Muscle Quantitative Nuclear Magnetic Resonance Imaging and Spectroscopy as an Outcome Measure for Clinical TrialsQuantitative Magnetic Resonance Imaging of Skeletal Muscle Disease.Assessment of intramuscular lipid and metabolites of the lower leg using magnetic resonance spectroscopy in boys with Duchenne muscular dystrophy.Muscle Quantitative MR Imaging and Clustering Analysis in Patients with Facioscapulohumeral Muscular Dystrophy Type 1Longitudinal Evaluation of Muscle Composition Using Magnetic Resonance in 4 Boys With Duchenne Muscular Dystrophy: Case Series.Whole-body magnetic resonance imaging evaluation of facioscapulohumeral muscular dystrophySerum proteomic profiling reveals fragments of MYOM3 as potential biomarkers for monitoring the outcome of therapeutic interventions in muscular dystrophies.Comparison of Multi-Echo Dixon Methods with Volume Interpolated Breath-Hold Gradient Echo Magnetic Resonance Imaging in Fat-Signal Fraction Quantification of Paravertebral MuscleMuscle MRI Findings in Childhood/Adult Onset Pompe Disease Correlate with Muscle Function.Combined quantification of fatty infiltration, T 1-relaxation times and T 2*-relaxation times in normal-appearing skeletal muscle of controls and dystrophic patients.Multicenter prospective longitudinal study of magnetic resonance biomarkers in a large duchenne muscular dystrophy cohort.Treatment with L-citrulline and metformin in Duchenne muscular dystrophy: study protocol for a single-centre, randomised, placebo-controlled trialEstimation of net muscle volume in patients with muscular dystrophy using muscle CT for prospective muscle volume analysis: an observational study.Treatment with L-citrulline in patients with post-polio syndrome: study protocol for a single-center, randomised, placebo-controlled, double-blind trial.Evaluation of an imaging biomarker, Dixon quantitative chemical shift imaging, in Gaucher disease: lessons learned.MRI proton density fat fraction is robust across the biologically plausible range of triglyceride spectra in adults with nonalcoholic steatohepatitis.Long-term follow-up of MRI changes in thigh muscles of patients with Facioscapulohumeral dystrophy: A quantitative study.Longitudinal characterization of biomarkers for spinal muscular atrophy.Muscle imaging in inherited and acquired muscle diseases.Longitudinal MRI quantification of muscle degeneration in Duchenne muscular dystrophy.Longitudinal functional and NMR assessment of upper limbs in Duchenne muscular dystrophy.Investigating the quantitative fidelity of prospectively undersampled chemical shift imaging in muscular dystrophy with compressed sensing and parallel imaging reconstruction.Quantifying fat replacement of muscle by quantitative MRI in muscular dystrophy.Sensitivity of chemical shift-encoded fat quantification to calibration of fat MR spectrum.Magnetic resonance imaging of the proximal upper extremity musculature in boys with Duchenne muscular dystrophy.Multivoxel proton magnetic resonance spectroscopy in facioscapulohumeral muscular dystrophy.Muscle MRI of classic infantile pompe patients: Fatty substitution and edema-like changes.Advanced MRI Techniques for Muscle Imaging.T2 relaxation times are increased in Skeletal muscle of DMD but not BMD patients.Multi-slice MRI reveals heterogeneity in disease distribution along the length of muscle in Duchenne muscular dystrophy.Towards defining muscular regions of interest from axial magnetic resonance imaging with anatomical cross-reference: part II - cervical spine musculature.
P2860
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P2860
Comparison of dixon and T1-weighted MR methods to assess the degree of fat infiltration in duchenne muscular dystrophy patients.
description
2013 nî lūn-bûn
@nan
2013 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
name
Comparison of dixon and T1-wei ...... e muscular dystrophy patients.
@ast
Comparison of dixon and T1-wei ...... e muscular dystrophy patients.
@en
type
label
Comparison of dixon and T1-wei ...... e muscular dystrophy patients.
@ast
Comparison of dixon and T1-wei ...... e muscular dystrophy patients.
@en
prefLabel
Comparison of dixon and T1-wei ...... e muscular dystrophy patients.
@ast
Comparison of dixon and T1-wei ...... e muscular dystrophy patients.
@en
P2093
P2860
P356
P1476
Comparison of dixon and T1-wei ...... ne muscular dystrophy patients
@en
P2093
Andrew Webb
Beatrijs H Wokke
Carla S van Rijswijk
Clemens Bos
Holger Eggers
Monique Reijnierse
P2860
P304
P356
10.1002/JMRI.23998
P577
2013-01-04T00:00:00Z