Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations.
about
MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India.Safety, Tolerability, and Pharmacokinetics of SMT C1100, a 2-Arylbenzoxazole Utrophin Modulator, following Single- and Multiple-Dose Administration to Pediatric Patients with Duchenne Muscular Dystrophy.Dystrophin Distribution and Expression in Human and Experimental Temporal Lobe Epilepsy.Reversal of neurobehavioral social deficits in dystrophic mice using inhibitors of phosphodiesterases PDE5A and PDE9A.The experiences of patients with Duchenne muscular dystrophy in facing and learning about their clinical conditionsCurrent Perspectives in Autism Spectrum Disorder: From Genes to Therapy.Astroglial Scarring and Seizures: A Cell Biological Perspective on Epilepsy.Secondary Conditions Among Males With Duchenne or Becker Muscular Dystrophy.Myelination is delayed during postnatal brain development in the mdx mouse model of Duchenne muscular dystrophySleep Disorders in Childhood Neurogenetic Disorders.Learning disabilities in neuromuscular disorders: a springboard for adult lifeTiming 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.Development of a New Self-Reporting Instrument Measuring Benefits and Side Effects of Corticosteroids in Duchenne Muscular Dystrophy: Report from a Pilot Study.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.Diagnosis and management of Duchenne muscular dystrophy, part 3: primary care, emergency management, psychosocial care, and transitions of care across the lifespan.Semi-Automated Analysis of Diaphragmatic Motion with Dynamic Magnetic Resonance Imaging in Healthy Controls and Non-Ambulant Subjects with Duchenne Muscular Dystrophy.Cardiac specific expression of ∆H2-R15 mini-dystrophin normalized all ECG abnormalities and the end-diastolic volume in a 23-m-old mouse model of Duchenne dilated cardiomyopathy.Clinical and genetic characterisation of dystrophin-deficient muscular dystrophy in a family of Miniature Poodle dogs.An Unusual Triad in Pediatric Neurology: A Case Report on Cerebral Palsy, Epilepsy, and Duchenne Muscular Dystrophy.Duchenne and Becker muscular dystrophy in adolescents: current perspectives.Systemic AAV Micro-dystrophin Gene Therapy for Duchenne Muscular DystrophyNeurodevelopmental 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
Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh-hant
name
Neurodevelopmental, emotional, ...... ing dystrophin gene mutations.
@en
Neurodevelopmental, emotional, ...... ing dystrophin gene mutations.
@nl
type
label
Neurodevelopmental, emotional, ...... ing dystrophin gene mutations.
@en
Neurodevelopmental, emotional, ...... ing dystrophin gene mutations.
@nl
prefLabel
Neurodevelopmental, emotional, ...... ing dystrophin gene mutations.
@en
Neurodevelopmental, emotional, ...... ing dystrophin gene mutations.
@nl
P2093
P2860
P50
P356
P1476
Neurodevelopmental, emotional, ...... ying dystrophin gene mutations
@en
P2093
David H Skuse
Francesco Muntoni
Mariacristina Scoto
Marika Pane
Nicolas Deconinck
Valeria Ricotti
P2860
P356
10.1111/DMCN.12922
P577
2015-09-14T00:00:00Z