Reduced cerebral gray matter and altered white matter in boys with Duchenne muscular dystrophy.
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Nonmechanical Roles of Dystrophin and Associated Proteins in Exercise, Neuromuscular Junctions, and Brains.Proton Magnetic Resonance Spectroscopy Indicates Preserved Cerebral Biochemical Composition in Duchenne Muscular Dystrophy Patients.Diffusion tensor imaging study in Duchenne muscular dystrophy.Myelination is delayed during postnatal brain development in the mdx mouse model of Duchenne muscular dystrophyTiming and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy.Dystrophin Dp116: A yet to Be Investigated Product of the Duchenne Muscular Dystrophy Gene.Brain and heart magnetic resonance imaging/spectroscopy in duchenne muscular dystrophy.Cognitive flexibility deficits in a mouse model for the absence of full-length dystrophin.Effects of Sildenafil on Cerebrovascular Reactivity in Patients with Becker Muscular Dystrophy.Mismatch Negativity Recording in Children With Duchenne Muscular Dystrophy: A Preliminary Study Integrating Neurophysiological and Neuropsychological Results.Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations.Diagnosis and management of Duchenne muscular dystrophy, part 3: primary care, emergency management, psychosocial care, and transitions of care across the lifespan.Cognitive and Neurobehavioral Profile in Boys With Duchenne Muscular Dystrophy.Targeting muscle stem cell intrinsic defects to treat Duchenne muscular dystrophy.Altered somatosensory neurovascular response in patients with Becker muscular dystrophy.Influence of full-length dystrophin on brain volumes in mouse models of Duchenne muscular dystrophy.Dystrophin Cardiomyopathies: Clinical Management, Molecular Pathogenesis and Evolution towards Precision MedicineNeurodevelopmental Needs in Young Boys with Duchenne Muscular Dystrophy (DMD): Observations from the Cooperative International Neuromuscular Research Group (CINRG) DMD Natural History Study (DNHS)
P2860
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P2860
Reduced cerebral gray matter and altered white matter in boys with Duchenne muscular dystrophy.
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2014 nî lūn-bûn
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2014年の論文
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2014年学术文章
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name
Reduced cerebral gray matter a ...... h Duchenne muscular dystrophy.
@en
Reduced cerebral gray matter a ...... h Duchenne muscular dystrophy.
@nl
type
label
Reduced cerebral gray matter a ...... h Duchenne muscular dystrophy.
@en
Reduced cerebral gray matter a ...... h Duchenne muscular dystrophy.
@nl
prefLabel
Reduced cerebral gray matter a ...... h Duchenne muscular dystrophy.
@en
Reduced cerebral gray matter a ...... h Duchenne muscular dystrophy.
@nl
P2093
P2860
P50
P356
P1433
P1476
Reduced cerebral gray matter a ...... h Duchenne muscular dystrophy.
@en
P2093
Andrew Webb
Beatrijs H Wokke
Chiara S Straathof
Debby G Schrans
Erik W van Zwet
Eve M Dumas
Ieke B Ginjaar
Janneke C van den Bergen
Jos G Hendriksen
Mark A van Buchem
P2860
P304
P356
10.1002/ANA.24222
P577
2014-07-24T00:00:00Z