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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 ...

Learn about Fabry disease, an inherited disorder caused by deficiency of the alpha-galactosidase A enzyme, and Fabrazyme enzyme replacement therapy.

Provides information and support for people with Fabry disease, their caregivers and families, and their health care providers.

Information about the group and this disease. Join the group free of charge and receive a newsletter.

Dedicated to raising awareness of the genetic disorder known as MCAD deficiency and the importance of early detection.

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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.

The Ara Parseghian Medical Research Foundation's goal is to find a cure for the devastating Niemann-Pick Type C disease.