Study on a family with anderson--Fabry's disease and associated familial spastic paraplegia.

Author:

Pierides A M,Holti G,Crombie A L,Roberts D F,Gardiner S E,Colling A,Anderson J

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference25 articles.

1. A case of angeio-keratoma. British J7ournal of;Anderson, W.;Dermatology,1898

2. Fabry's disease. A correlative clinical, morphologic and biochemical study;Bagdade, J.D.; Parker, F.; Ways, P.O.; Morgan, T.E.; Lagunoff, D.; Eidelman, S.;Laboratory Investigation,1968

3. Enzymatic defect in Fabry's disease;Brady, R.O.; Gal, A.E.; Bradley, R.M.; Martensson, E.; Warshaw, A.L.; Laster, L.;New England Journal of Medicine,1967

4. Kidney transplanatation in Fabry's disease;Biihler, F.R.; Thiel, G.; Dubach, U.C.; Enderlin, F.; Gloor, F.; Tholen, H.;British Medical,1973

5. Fabry's disease: general clinical aspects, Archives Belges de Dermatologie et de Syphiligraphie;Carton, D.,1972

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