Pages that link to "Q34963315"
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The following pages link to Quantitative muscle MRI as an assessment tool for monitoring disease progression in LGMD2I: a multicentre longitudinal study (Q34963315):
Displaying 50 items.
- Multi-parametric MRI at 14T for muscular dystrophy mice treated with AAV vector-mediated gene therapy (Q27308877) (← links)
- (Q28397480) (← links)
- Association of Quadriceps Muscle Fat With Isometric Strength Measurements in Healthy Males Using Chemical Shift Encoding-Based Water-Fat Magnetic Resonance Imaging (Q28833812) (← links)
- Report on the 3rd Ottawa International Conference on Neuromuscular Biology, Disease and Therapy - September 24-26, 2015, Ottawa, Canada. (Q30355125) (← links)
- In vitro and in vivo comparison of two-, three- and four-point Dixon techniques for clinical intramuscular fat quantification at 3 T. (Q30780225) (← links)
- Automatic and quantitative assessment of regional muscle volume by multi-atlas segmentation using whole-body water-fat MRI. (Q30841856) (← links)
- Skeletal muscle quantitative nuclear magnetic resonance imaging follow-up of adult Pompe patients (Q30906462) (← links)
- Quantitative NMRI and NMRS identify augmented disease progression after loss of ambulation in forearms of boys with Duchenne muscular dystrophy. (Q30983066) (← links)
- MRI biomarker assessment of neuromuscular disease progression: a prospective observational cohort study. (Q31019878) (← links)
- Quantifying disease activity in fatty-infiltrated skeletal muscle by IDEAL-CPMG in Duchenne muscular dystrophy (Q31126675) (← links)
- Skeletal Muscle Quantitative Nuclear Magnetic Resonance Imaging and Spectroscopy as an Outcome Measure for Clinical Trials (Q31142754) (← links)
- Magnetic resonance imaging and spectroscopy assessment of lower extremity skeletal muscles in boys with Duchenne muscular dystrophy: a multicenter cross sectional study (Q34155950) (← links)
- Examination of effects of corticosteroids on skeletal muscles of boys with DMD using MRI and MRS. (Q34171004) (← links)
- Oculopharyngeal muscular dystrophy as a paradigm for muscle aging (Q34449597) (← links)
- Muscle Quantitative MR Imaging and Clustering Analysis in Patients with Facioscapulohumeral Muscular Dystrophy Type 1 (Q35693421) (← links)
- Simultaneous muscle water T2 and fat fraction mapping using transverse relaxometry with stimulated echo compensation (Q35905353) (← links)
- Feasibility of MR-Based Body Composition Analysis in Large Scale Population Studies (Q36142944) (← links)
- Combined quantification of fatty infiltration, T 1-relaxation times and T 2*-relaxation times in normal-appearing skeletal muscle of controls and dystrophic patients (Q36319212) (← links)
- Multicenter prospective longitudinal study of magnetic resonance biomarkers in a large duchenne muscular dystrophy cohort. (Q37114363) (← links)
- MRI quantifies neuromuscular disease progression (Q37123866) (← links)
- The Classification, Natural History and Treatment of the Limb Girdle Muscular Dystrophies (Q37610524) (← links)
- Long-term follow-up of MRI changes in thigh muscles of patients with Facioscapulohumeral dystrophy: A quantitative study (Q38608088) (← links)
- Clinical Trials in Spinal and Bulbar Muscular Atrophy-Past, Present, and Future (Q38634370) (← links)
- Longitudinal characterization of biomarkers for spinal muscular atrophy. (Q38685408) (← links)
- Myopathology in times of modern imaging (Q38767197) (← links)
- Investigating the quantitative fidelity of prospectively undersampled chemical shift imaging in muscular dystrophy with compressed sensing and parallel imaging reconstruction (Q39292845) (← links)
- Quantifying fat replacement of muscle by quantitative MRI in muscular dystrophy. (Q39409381) (← links)
- Magnetic Resonance Imaging in a large cohort of facioscapulohumeral muscular dystrophy patients: pattern refinement and implications for clinical trials. (Q39905506) (← links)
- Towards a European Registry and Biorepository for Patients with Spinal and Bulbar Muscular Atrophy. (Q40991752) (← links)
- Congenital myopathies: clinical phenotypes and new diagnostic tools (Q47134873) (← links)
- Sciatic neurosteatosis: Relationship with age, gender, obesity and height. (Q47180102) (← links)
- Limb-girdle muscular dystrophy type 2I: two Chinese families and a review in Asian patients (Q47767530) (← links)
- Skeletal muscle contractile properties in a novel murine model for limb girdle muscular dystrophy 2i. (Q47874181) (← links)
- MRI as outcome measure in facioscapulohumeral muscular dystrophy: 1-year follow-up of 45 patients (Q48131113) (← links)
- Muscle MRI of classic infantile pompe patients: Fatty substitution and edema-like changes (Q48495872) (← links)
- Precision of MRI-based body composition measurements of postmenopausal women. (Q48504390) (← links)
- Broadening the imaging phenotype of dysferlinopathy at different disease stages (Q50538847) (← links)
- Contractile properties are disrupted in Becker muscular dystrophy, but not in limb girdle type 2I. (Q52673776) (← links)
- Skeletal muscle magnetic resonance biomarkers correlate with function and sentinel events in Duchenne muscular dystrophy. (Q55282480) (← links)
- Advanced body composition assessment: from body mass index to body composition profiling. (Q55404959) (← links)
- Magnetic Resonance Imaging Findings in the Muscle Tissue of Patients with Limb Girdle Muscular Dystrophy Type 2I Harboring the Founder Mutation c.545A>G in the FKRP Gene. (Q55555004) (← links)
- Non-invasive tracking of disease progression in young dystrophic muscles using multi-parametric MRI at 14T (Q58549465) (← links)
- Exploration of New Contrasts, Targets, and MR Imaging and Spectroscopy Techniques for Neuromuscular Disease - A Workshop Report of Working Group 3 of the Biomedicine and Molecular Biosciences COST Action BM1304 MYO-MRI (Q64236140) (← links)
- Advances in Quantitative Imaging of Genetic and Acquired Myopathies: Clinical Applications and Perspectives (Q64249359) (← links)
- Natural history of limb girdle muscular dystrophy R9 over 6 years: searching for trial endpoints. (Q64885267) (← links)
- MRI of trunk muscles and motor and respiratory function in patients with myotonic dystrophy type 1. (Q64903672) (← links)
- Follow-up of late-onset Pompe disease patients with muscle magnetic resonance imaging reveals increase in fat replacement in skeletal muscles (Q90022892) (← links)
- Association of paraspinal muscle water-fat MRI-based measurements with isometric strength measurements (Q90264446) (← links)
- Quantitative muscle MRI to follow up late onset Pompe patients: a prospective study (Q90322484) (← links)
- Quantitative nuclear magnetic resonance imaging detects subclinical changes over 1 year in skeletal muscle of GNE myopathy (Q90736942) (← links)