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Fabry disease is an X-linked inborn error of metabolism wherein deficiency of a lysosomal enzyme results in systemic deposition of glycosphingolipids. Storage d

Joe's story was developed to help explain Fabry disease and its treatment from the perspective of a ten year old.

Presents clinical, biochemical, and genetic information concerning those metabolic anomalies grouped under inborn errors of metabolism.

This fourth edition of the Oxford Textbook of Clinical Nephrology builds on the success and international reputation of the publication as an important resource

Research into perspiration has developed dramatically during the last 15 years, continually improving our understanding of the pathogenesis of sweating disorder