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Data from: Noninvasive assessment of respiratory muscle strength and activity in Myotonic dystrophy
- 负责人:
- DOI:
- doi:10.5061/dryad.dc464
- 摘要:
- with Myotonic dystrophy type 1 (DM1) compared with healthy subjects. Design and methods Quasi-experimental observational study with control group. MRR of inspiratory muscles
Data from: Genetic determinants of disease severity in the myotonic dystrophy type 1 OPTIMISTIC cohort
- 负责人:
- DOI:
- doi:10.5061/dryad.t063q70
- 摘要:
- Background: Myotonic dystrophy type 1 (DM1) is caused by expansion of an unstable CTG repeat in the DMPK gene. The average number of repeats reported
Data from: Lower extremity muscle pathology in myotonic dystrophy type 1 assessed by quantitative MRI
- 负责人:
- DOI:
- doi:10.5061/dryad.4nb96c1
- 摘要:
- muscles of myotonic dystrophy type 1 (DM1) patients. Methods: We acquired images covering these muscles in 33 genetically and clinically well-characterized DM1 patients and 10
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