Psychiatric and neurodevelopmental aspects of Becker muscular dystrophy
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference19 articles.
1. Mild and severe muscular dystrophy associated with deletions in Xp21 of the human x chromosome;Davies;J Med Genet,1988
2. Dystrophin and mutations: one gene, several proteins, multiple phenotypes;Muntoni;Lancet Neurol,2003
3. The muscular dystrophies;Emery;Lancet,2002
4. An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus;Monaco;Genomics,1988
5. Social involvement issues in patients with Becker muscular dystrophy: a questionnaire survey of subjects from a patient registry;Mori-Yoshimura;Brain Dev,2018
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1. Prevalence of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder in Individuals With Dystrophinopathy at a Tertiary Care Center in Chicago;Pediatric Neurology;2024-09
2. The use of the drug ataluren for the treatment of patients with Duchenne muscular dystrophy in real clinical practice;L.O. Badalyan Neurological Journal;2024-07-31
3. Social difficulties and care burden of adult Duchenne muscular dystrophy in Japan: a questionnaire survey based on the Japanese Registry of Muscular Dystrophy (Remudy);Orphanet Journal of Rare Diseases;2024-04-30
4. The Importance of a PM&R Consultation for Becker Muscular Dystrophy Patients Admitted with Cardiomyopathy;Case Reports in Cardiology;2024-03-22
5. Prevalence of Attention Deficit Hyperactivity Disorder and Autism Spectrum Disorder in Children with Duchenne and Becker Muscular Dystrophy in Chicago;2024
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