Case Study: Facioscapulohumeral Muscular Dystrophy

Kling L. Eagle M. Haggerty I.D. Roberts E. Straub V. Bushby K.M. (2006). Severe phenotype in infantile facioscapulohumeral muscular dystrophy. Neuromuscular Disorders 16: doi:10.1016/j.nmd.2006.06.008.

Padberg G.W. Frants R.R. Brouwer O.F. Wijmenga C. Bakker E. Sandkuijl L.A. (1995). Facioscapulohumeral muscular dystrophy in the Dutch population. Muscle & Nerve Suppl 2: S81–4. doi:10.1002/mus.880181315.

Tawil R. Figlewicz D.A. Griggs R.C. Weiffenbach B. , the FSH Consortium. (1998). Facioscapulohumeral dystrophy: A distinct regional myopathy with a novel molecular pathogenesis. Annals of Neurology 43: p. 279–82. doi:10.1002/ana.410430303.

Tawil R. Van der Maarel S.M. (2006). Facioscapulohumeral muscular dystrophy. Muscle & Nerve 34: p. 1–15.

Van der Kooi A.J. Visser M.C. Rosenberg N. (2000). Extension of the clinical range of facioscapulohumeral dystrophy: Report of six cases. Journal of Neurology, Neurosurgery & Psychiatry 69: p. 114–6. doi:10.1136/jnnp.69.1.114.