Quantitative magnetic resonance imaging in limb-girdle muscular dystrophy 2I: a multinational cross-sectional study. - Wikidata - wikimedia - TriplyDB

Quantitative magnetic resonance imaging in limb-girdle muscular dystrophy 2I: a multinational cross-sectional study.

Quantitative magnetic resonance imaging in limb-girdle muscular dystrophy 2I: a multinational cross-sectional study.

http://www.wikidata.org/entity/Q37610370

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Association of Quadriceps Muscle Fat With Isometric Strength Measurements in Healthy Males Using Chemical Shift Encoding-Based Water-Fat Magnetic Resonance Imaging Report on the 3rd Ottawa International Conference on Neuromuscular Biology, Disease and Therapy - September 24-26, 2015, Ottawa, Canada.Nutritional status evaluation in patients affected by bethlem myopathy and ullrich congenital muscular dystrophy.Muscle MRI in muscular dystrophies The Classification, Natural History and Treatment of the Limb Girdle Muscular Dystrophies Muscle imaging in inherited and acquired muscle diseases.Magnetic resonance imaging patterns of muscle involvement in genetic muscle diseases: a systematic review.Quantifying fat replacement of muscle by quantitative MRI in muscular dystrophy.3D multimodal spatial fuzzy segmentation of intramuscular connective and adipose tissue from ultrashort TE MR images of calf muscle.Quantification of intramuscular fat in patients with late-onset Pompe disease by conventional magnetic resonance imaging for the long-term follow-up of enzyme replacement therapy.Limb-girdle muscular dystrophy type 2I: two Chinese families and a review in Asian patients.A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population.Volume measurements of individual muscles in human quadriceps femoris using atlas-based segmentation approaches.Broadening the imaging phenotype of dysferlinopathy at different disease stages.Advanced MRI Techniques for Muscle Imaging.Multi-slice MRI reveals heterogeneity in disease distribution along the length of muscle in Duchenne muscular dystrophy.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.Muscle MRI in patients with dysferlinopathy: pattern recognition and implications for clinical trials The clinical spectrum and genetic variability of limb-girdle muscular dystrophy in a cohort of Chinese patients

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Quantitative magnetic resonance imaging in limb-girdle muscular dystrophy 2I: a multinational cross-sectional study.

http://www.wikidata.org/entity/Q37610370

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bilimsel makale

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scientific article published on 28 February 2014

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Quantitative magnetic resonanc ...... ational cross-sectional study.

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Quantitative magnetic resonanc ...... ational cross-sectional study.

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JOURNAL.PONE.0090377

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Quantitative magnetic resonanc ...... ational cross-sectional study.

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Anna Coombs

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Anna Mayhew

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Christopher D J Sinclair

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Hanns Lochmuller

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Jasper M Morrow

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John Vissing

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Kate Bushby

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Kieren G Hollingsworth

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Liz Dewar

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Marie-Louise Sveen

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Statistical methods for assessing agreement between two methods of clinical measurement

Two-point Dixon technique for water-fat signal decomposition with B0 inhomogeneity correction.

Three-point Dixon technique for true water/fat decomposition with B0 inhomogeneity correction.

A founder mutation in Anoctamin 5 is a major cause of limb-girdle muscular dystrophy.

Neuromuscular imaging in inherited muscle diseases

FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients

Muscle imaging in clinical practice: diagnostic value of muscle magnetic resonance imaging in inherited neuromuscular disorders.

Simple proton spectroscopic imaging.

Muscle MRI in inherited neuromuscular disorders: past, present, and future.

The phenotype of limb-girdle muscular dystrophy type 2I.

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scholarly article

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10.1371/JOURNAL.PONE.0090377

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John S Thornton

Jean-Yves Hogrel

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