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Facioscapulohumeral muscular dystrophy 1a

Also Known As:
FSHD1A; FSHMD1A; Facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles; Facioscapulohumeral muscular dystrophy, infantile; Landouzy-dejerine muscular dystrophy; Muscular dystrophy, facioscapulohumeral, type 1a
Networked: 10 relevant articles (0 outcomes, 1 trials/studies)

Bio-Agent Context: Research Results

Experts

1. van der Maarel, Silvère M: 2 articles (07/2004 - 06/2004)
2. Padberg, George W: 2 articles (07/2004 - 06/2004)
3. Frants, Rune R: 2 articles (07/2004 - 06/2004)
4. Lemmers, Richard J L F: 2 articles (07/2004 - 06/2004)
5. Magdinier, Frédérique: 1 article (12/2015)
6. Batten, Kimberly: 1 article (12/2015)
7. Shay, Jerry W: 1 article (12/2015)
8. Wright, Woodring E: 1 article (12/2015)
9. Robin, Jérôme D: 1 article (12/2015)
10. Stadler, Guido: 1 article (12/2015)

Related Diseases

1. Facioscapulohumeral Muscular Dystrophy
2. Inflammation
3. Inborn Genetic Diseases (Disease, Hereditary)
4. Duchenne Muscular Dystrophy (Muscular Dystrophy, Becker)
5. Muscular Dystrophies (Muscular Dystrophy)