Results 151 to 160 of about 1,757 (183)
Jejunal Diverticulosis With Perforation as a Complication of Fabry's Disease
, 1984 Lawrence S. Friedman +5 more
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Comparative pharmacokinetics and pharmacodynamics of two formulations of agalsidase beta (agalsidase Biosidus) and Fabrazyme® by intravenous infusion in healthy male volunteers. [PDF]
Mol Genet Metab RepBerstein V +9 more
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Quality of Life in patients with Fabry's disease: Investigation with the SF-36 questionnaire
, 2012 Blohm, Elisabeth
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Fabry's disease: the search for a regulatory gene mutation in man.
, 1972 H. E. Sutton, Gilbert S. Omenn
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Dialysis Vintage and Symptom Burden in Hemodialysis: A Comprehensive Analysis. [PDF]
Nurs Health SciYan S, Wang Y, Li Z, Wang D, Yao D.
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Cutaneous manifestations of Fabry disease: A systematic review. [PDF]
J DermatolAl-Chaer RN +4 more
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Bridging the gap: Exploring the intercurrent relationship between knee osteoarthritis and cerebral small vessel disease. [PDF]
Caspian J Intern MedMohamad Ghazali M +4 more
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The Lancet, 2008
Fabry's disease is an X-linked lysosomal storage disorder caused by abnormalities in the GLA gene, which leads to a deficiency in alpha-galactosidase A. The consequent abnormal accumulation of glycosphingolipids results in several clinical signs and symptoms and substantial morbidity and mortality.
Yuri A, Zarate, Robert J, Hopkin
+7 more sources
Fabry's disease is an X-linked lysosomal storage disorder caused by abnormalities in the GLA gene, which leads to a deficiency in alpha-galactosidase A. The consequent abnormal accumulation of glycosphingolipids results in several clinical signs and symptoms and substantial morbidity and mortality.
Yuri A, Zarate, Robert J, Hopkin
+7 more sources