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2009 AUG 17 ... was marked by a significant achievement for Amicus with our lead program, Amigal for Fabry disease, entering Phase 3 development." Crowley continued, "This is a major step for the ...
2009 AUG 10 ... to recent research published in the journal Nephrology Dialysis Transplantation, "In Fabry disease, progressive glycolipid accumulation leads to organ damage and early demise, but the ...
2009 AUG 10 ... and mutations in these enzymes lead to the lipid metabolism disorders Gaucher and Fabry disease, respectively. We have investigated the structure and stability of GCase and alpha-Gal A ...
2009 NOV 23 ... According to recent research from Paris, France, "Fabry disease (OMIM 301 500) is an X-linked lysosomal storage disease. Neurological symptoms in...
2009 NOV 1 ... walking distance in patients with moderate intermittent claudication," wrote R. Fabry and colleagues. The researchers concluded: "This effect, which was ... Care Medicine, Intermittent Claudication, Quality of Life, Therapy, Treatment, Vascular Disease. This article was prepared by Pharma Investments, Ventures & Law Weekly ...
2009 OCT 5 ... patient demand through October. Dose conservation guidelines were implemented by the Fabry physician and patient community to help ensure that the reduced product supply was ... The company's products and services are focused on rare inherited disorders, kidney disease, orthopaedics, cancer, transplant and immune disease, and diagnostic testing. Genzyme's ...
2009 NOV 23 ... Many great surgeons of that time (including Pare, Cabrol, Servetto, Scultetus, Tulp, Fabry von Hilded, etc.) advanced the science of surgery. Interestingly, Bartoleny Gabrol ... of Cancer Care. According to a study from Athens, Greece, "Cancer was known as a disease since prehistoric times. Management of breast cancer evolved slowly through centuries in ...
2009 AUG 10 ... According to a study from Mainz, Germany, "Although Fabry disease is X linked and considered to affect primarily male hemizygotes, female heterozygotes ...
2009 OCT 12 ... According to a study from Buenos Aires, Argentina, "Fabry disease is a rare, X-linked lysosomal storage disease caused by an inborn deficiency of ...
2009 OCT 12 ... According to recent research from Seoul, South Korea, "Fabry disease is a lysosomal storage disease caused by a deficiency of alpha-galactosidase A, which ...
2009 AUG 31 ... blood spots from 10 patients affected by ''Pompe'', 6 by ''Gaucher'', 12 by ''Fabry'', 3 by ''Niemann-Pick'' A/B, and 2 by ''Krabbe'' diseases. Reference values ... normal range. In heterozygous carriers (18 for Fabry, 10 for Pompe, and 4 for Gaucher disease) the activities were slightly lower than in control subjects," wrote G. Lamarca and ...
2009 NOV 2 ... for REPLAGAL® (agalsidase alfa), its enzyme replacement therapy for Fabry disease, by the end of the year. The Company also announces that a treatment protocol for ...
2009 NOV 2 ... (FDA) for REPLAGAL® (agalsidase alfa), its enzyme replacement therapy for Fabry disease, by the end of the year. The Company also announces that a treatment protocol for ...
2009 NOV 1 ... globotriaosylceramide (Gb3) is known to be associated with Gb3-related diseases, such as Fabry disease. The Gb3 synthase gene (Gb3S) codes for alpha 1,4-galactosyltransferase, which is a key ...
