Facioscapulohumeral muscular dystrophy 1a
PROM
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: 4
relevant articles (0 outcomes,
0 trials/studies)
Disease Context: Research Results
Experts
1. | MacKenzie, Jennifer J:
1 article
(08/2014)
|
2. | Piteau, Shalea J:
1 article
(08/2014)
|
3. | Rossiter, John P:
1 article
(08/2014)
|
4. | Smith, R Garth:
1 article
(08/2014)
|
5. | Hauerslev, S:
1 article
(09/2013)
|
6. | Hertz, J M:
1 article
(09/2013)
|
7. | Krag, T O:
1 article
(09/2013)
|
8. | Vissing, J:
1 article
(09/2013)
|
9. | Ørngreen, M C:
1 article
(09/2013)
|
10. | Ansseau, Eugénie:
1 article
(08/2007)
|
Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Facioscapulohumeral muscular dystrophy 1a: