Evidence-based guideline summary: Evaluation, diagnosis, and management of facioscapulohumeral muscular dystrophy
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical)
Reference36 articles.
1. Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy
2. Facioscapulohumeral muscular dystrophy
3. A Prospective, Quantitative Study of the Natural History of Facioscapulohumeral Muscular Dystrophy (FSHD): Implications for Therapeutic Trials
4. Facioscapulohumeral muscular dystrophy: a prospective study of weakness and functional impairment
5. Transmission of de-novo mutation associated with facioscapulohumeral muscular dystrophy
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2. Fasyoskapulohumeral Musküler Distrofili Bireylerde Tedavi Yaklaşımları: Derleme Makalesi;Fenerbahçe Üniversitesi Sağlık Bilimleri Dergisi;2024-08-26
3. The yield of genetic workup for middle-aged and elderly patients with neurological disorders in a real-world setting;Journal of the Neurological Sciences;2024-08
4. French National Protocol for diagnosis and care of facioscapulohumeral muscular dystrophy (FSHD);Journal of Neurology;2024-07-02
5. Advanced Heart Failure Therapies in Neuromuscular Diseases;Current Treatment Options in Cardiovascular Medicine;2024-06-25
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