Facioscapulohumeral muscular dystrophy
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical),Neurology
Reference83 articles.
1. Hearing loss in facioscapulohumeral muscular dystrophy
2. Facioscapulohumeral dystrophy presenting in infancy with facial diplegia and sensorineural deafness
3. Facioscapulohumeral dystrophy associated with hearing loss and coats syndrome
4. Inflammatory facioscapulohumeral muscular dystrophy and coats syndrome
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1. SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation;Nature Communications;2024-02-27
2. Mimics of Immune-Mediated Myopathy;Immune-Mediated Myopathies and Neuropathies;2023
3. Myositis Mimics: The Differential Diagnosis of Myositis;Managing Myositis;2019-12-15
4. Effect of taping on scapular kinematics of patients with facioscapulohumeral muscular dystrophy;Neurological Sciences;2019-04-09
5. The French National Registry of patients with Facioscapulohumeral muscular dystrophy;Orphanet Journal of Rare Diseases;2018-12
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