Beschreibung
Produktdetails
Einband
Taschenbuch
Erscheinungsdatum
14.05.2012
Abbildungen
XVI, 39 illus., schwarz-weiss Illustrationen
Herausgeber
P. Durand + weitereVerlag
Springer BerlinSeitenzahl
220
Maße (L/B/H)
24,4/17/1,4 cm
Gewicht
422 g
Auflage
Softcover reprint of the original 1st ed. 1982
Sprache
Englisch
ISBN
978-3-642-51584-2
On starting to write the preface it occured to the editors that it might be a good idea to incorporate so me organizational thoughts. First of all, why have. we organized this book on «Glycoprotein storage diseases", an unfamiliar area of pathology unlikely to be encountered in practice? In preparing such a volume we considered that in the past ten years there has been a large amount of intensive research activity on glycoproteinoses and no detailed review has been entirely devoted to this subject. This research has led to new information about hereditary mental retardation and progressive neurologie degeneration, and as clinicians we are impressed with its clinical importance. This volume is intended to represent for the uninitiated as weH as for the expert a summary of studies on dis orders of glycoprotein catabolism written by experts in each area. Each author has written with freedom about his particular experience, describing the establishment and development of his investigations, his methods, the utility and limitations of his work and eventual sources of problems. We are grateful for their many fundamental studies and for their having generously accepted to partecipate in this book. The Editors Acknowledgements We wish to express our gratitude to our friends and colleagues G. Romeo, W.S. Sly and G. Tettamanti whose criticism and suggestions have significantly improved the quality of particular chapters or sections.
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