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Fabrazyme ® | Fabry Disease Enzyme Replacement Therapy Treatment (agalsidase beta)
Описание: Learn about Fabry disease, an inherited disorder caused by deficiency of the alpha-galactosidase A enzyme, and Fabrazyme enzyme replacement therapy.
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Pulsus Group Inc, the medical peer review publisher, publishes the work of medical researchers in a manner that exemplifies the highest standards in research ...
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Information about an ongoing observational database that tracks the natural history and clinical outcomes of patients with this disease.
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Learn about ORENCIA® (abatacept) and review the Important Safety Information and Prescribing Information.
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Provides information and support for people with Fabry disease, their caregivers and families, and their health care providers.
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Information about the group and this disease. Join the group free of charge and receive a newsletter.
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Dedicated to raising awareness of the genetic disorder known as MCAD deficiency and the importance of early detection.
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克服のため試した化粧品などの感想を掲載。
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The mission of NINDS is to reduce the burden of neurological disease - a burden borne by every age group, by every segment of society, by people all over the world.
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