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Lysosomal Storage Disorders - John A. Barranger

Lysosomal Storage Disorders

By: John A. Barranger (Editor), Mario Cabrera-Salazar (Editor)

Hardcover | 1 October 2007

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The knowledge of lysosomal biology and the consequences of its dysfunction have increased dramatically in the past 60 years. Research of these disorders has moved from diseases with unknown etiology to disorders with clear and defined pathophysiology and some of them have benefited from the development of disease specific therapeutics. This book describes the nature of the lysosomal dysfunction and diseases as well as potential future treatments and therapies. Disease specific chapters provide thorough reviews of the clinical features of lysosomal storage disorders, their molecular basis and the commercial or experimental therapeutic approaches sought in this area. This is an invaluable resource for researchers in biochemical and molecular genetics, enzyme therapy, and gene transfer.

Industry Reviews

From the reviews:

"The authors have brought together an excellent group of contributors to provide an introduction to lysosomal storage disorders (LSDs). ... It is oriented to serve individuals working in the field of LSDs, but it also would provide a good base of knowledge for graduate students, medical residents, or clinical genetics physicians who wish to update their understanding of the lysosome pathology and function. ... With this unique book, the authors have provided a well thought out source of information on lysosomal disorders." (Luis F. Escobar, Doody's Review Service, July, 2009)

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