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.

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

A review of childhood neurodegenerative and other progressive but non-degenerative disorders to guide their diagnosis and management.

Thoroughly updated for its Third Edition, this text will be the definitive reference on autonomic nervous system disorders, for practicing and academic neurolog