Facioscapulohumeral Dystrophy

Awerbuch GI, Nigro MA, Wishnow R. Beevor's sign and facioscapulohumeral dystrophy. Arch Neurol 1990;47:1208-1209.

Brouwer OF, Padberg GW, Ruys CJM, Brand R, de Laat JAPM, Grote JJ. Hearing loss in facioscapulohumeral muscular dystrophy. Neurology 1991;41:1878-1881.

Fitzsimons RB, Gurwin EB, Bird AC. Retinal vascular abnormalities in facioscapulohumeral muscular dystrophy: a general association with genetic and therapeutic implications. Brain 1987;110:631-648.

Tawil R, McDermott MP, Mendell JR, et al. Facioscapulohumeral muscular dystrophy (FSHD); design of natural history and results of baseline testing. Neurology 1994;44:442-446.

Tawil R, Figlewicz DA, Griggs RC, Weiffenbach B. FSH Consortium Facioscapulohumeral dystrophy: a distinct regional myopathy with a novel molecular pathogenesis. Ann Neurol 1988;43:279-282.

van der Kooi AJ, Visser MC, Rosenberg N, et al. Extension of the clinical range of facioscapulohumeral dystrophy: report of six cases. J Neurol Neurosurg Psychiatry 2000;69:114-116.

Wijmenga C, Hewitt JE, Sandkuijl LA, et al. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy. Nature Genet 1992;2:26-30.

0 0

Post a comment