A rare association between Fabry’s disease and granulomatosis with polyangiitis: a potential pathogenic link
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
http://link.springer.com/content/pdf/10.1186/1471-2369-15-157.pdf
Reference16 articles.
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2. Nagano Y, Nakashima H, Fukuhara Y, Shimmoto M, Oshima A, Ikari Y, Mori Y, Sakuraba H, Suzuki Y: Hypertrophic cardiomyopathy in late-onset variant of Fabry’s disease with high residual activity of alpha-galactosidase A. Clin Genet. 1991, 39: 233-237.
3. Schiffmann R, Kopp JB, Austin HA, Sabnis S, Moore DF, Weibel T, Balow JE, Brady RO: Enzyme replacement therapy in Fabry disease: A randomized controlled trial. JAMA. 2001, 285: 2743-2749. 10.1001/jama.285.21.2743.
4. MacDermot KD, Holmes A, Miners AH: Anderson–Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males. J Med Genet. 2001, 38: 750-760. 10.1136/jmg.38.11.750.
5. MacDermot KD, Holmes A, Miners AH: Anderson–Fabry disease: clinical manifestations and impact of disease in a cohort of 60 obligate carrier females. J Med Genet. 2001, 38: 769-775. 10.1136/jmg.38.11.769.
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