Magnetic resonance imaging changes in Fabry disease

Author:

Ginsberg Lionel,Manara Renzo,Valentine Alan,Kendall Brian,Burlina Alessandro

Publisher

Wiley

Subject

General Medicine,Pediatrics, Perinatology and Child Health

Reference15 articles.

1. DesnickRJ, IoannouYA, EngCM. α-Galactosidase A deficiency: Fabry disease. In: ScriverCR, BeaudetAL, SlyWS, ValleD, editors. The metabolic and molecular basis of inherited disease . 8th edn. New York: McGraw-Hill2001p: 3733–74.

2. Ginsberg, L and Valentine, A and Mehta, A. (2005) Neurological rarity-Fabry disease Practical Neurology, 5, pp. 110 - 3.

3. Mehta, A and Ginsberg, L. (2005) Natural history of the cerebrovascular complications of Fabry disease Acta Paediatr, 94(Suppl 447), pp. 24 - 7.

4. Rolfs, A and Bottcher, T and Zschiesche, M and Morris, P and Winchester, B and Bauer, P and (2005) Prevalence of Fabry disease in patients with cryptogenic stroke: a prospective study Lancet, 366, pp. 1794 - 6.

5. Mitsias, P and Levine, SR. (1996) Cerebrovascular complications of Fabry's disease Ann Neurol, 40, pp. 8 - 17.

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