Magnetic Resonance Monitoring of Disease Progression in mdx Mice on Different Genetic Backgrounds.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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2017年學術文章

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Magnetic Resonance Monitoring ...... Different Genetic Backgrounds.

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Magnetic Resonance Monitoring ...... Different Genetic Backgrounds.

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Magnetic Resonance Monitoring ...... Different Genetic Backgrounds.

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P1476

Magnetic Resonance Monitoring ...... Different Genetic Backgrounds.

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P2093

Abhinandan Batra

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Glenn A Walter

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Krista Vandenborne

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Ravneet Vohra

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Sean C Forbes

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P2860

Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation

Assessment of Myocardial Fibrosis in Mice Using a T2*-Weighted 3D Radial Magnetic Resonance Imaging Sequence

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Magnetic Resonance Imaging Is Sensitive to Pathological Amelioration in a Model for Laminin-Deficient Congenital Muscular Dystrophy (MDC1A)

Evaluation of Electrical Impedance as a Biomarker of Myostatin Inhibition in Wild Type and Muscular Dystrophy Mice

Chemical shift-based MRI to measure fat fractions in dystrophic skeletal muscle.

New insights on human skeletal muscle tissue compartments revealed by in vivo t2 NMR relaxometry.

Compartmental relaxation and diffusion tensor imaging measurements in vivo in lambda-carrageenan-induced edema in rat skeletal muscle.

Nuclear magnetic resonance measurement of skeletal muscle: anisotrophy of the diffusion coefficient of the intracellular water.

Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy.

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2060-2070

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scholarly article

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10.1016/J.AJPATH.2017.05.010

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English

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187

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2017-09-01T00:00:00Z

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28826559

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5809503

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