
Connective Tissue and Its Heritable Disorders
Molecular, Genetic, and Medical Aspects
Wiley (Publisher)
2nd Edition
Published on 10. May 2002
Book
Hardback
1202 pages
978-0-471-25185-9 (ISBN)
Article exhausted; check different version
Description
The Second Edition of Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects is the definitive reference text in its field, with over 40% more pages on the nature, diagnosis, and treatment of disease than its predecessor. Collecting new research on disorders detailed in the first edition as well as on those previously excluded, editors Peter Royce and Beat Steinmann provide the most up-to-date clinical and scientific information for medical specialists treating affected individuals. Features of this revised and updated volume include detailed reviews of the clinical diagnosis, mode of inheritance, risk of recurrence, and prenatal diagnosis of each inherited connective tissue disorder; a thorough description of the morphology of connective tissues; a completely updated and revised section on the biology of the extracellular matrix; and the addition of syndromes such as craniosyntosis, and disorders of sulfate metabolism. Obstetricians, radiologists, dermatologists, neurologists, and specialists in internal medicine, as well as cardiovascular, abdominal, and plastic surgeons will find Connective Tissue and Its Heritable Disorders to be an essential addition to their personal and professional libraries.
Reviews / Votes
".an excellent book that provides an invaluable resource on connective tissue and associated disorders. It should be available to all with a scientific or medical interest in this field." (Doody's Health)More details
Edition
2., Auflage
Language
English
Place of publication
New York
United States
Publishing group
John Wiley and Sons Ltd
Target group
College/higher education
Professional and scholarly
Edition type
Revised edition
Illustrations
tables
Dimensions
Height: 28.3 cm
Width: 22.5 cm
Thickness: 61 mm
Weight
4056 gr
ISBN-13
978-0-471-25185-9 (9780471251859)
Schweitzer Classification
Other editions
Additional editions

Peter M. Royce | Beat Steinmann
Connective Tissue and Its Heritable Disorders
Molecular, Genetic, and Medical Aspects
E-Book
03/2003
2nd Edition
Wiley
€381.99
Available for download
Previous edition
Peter M. Royce | Beat Steinmann
Connective Tissue and It's Heritable Disorders
Molecular, Genetic and Medical Aspects
Book
11/1992
Wiley
€468.74
Article exhausted; check for reprint
Content
Preface (Peter M. Royce and Beat Steinmann).
Acknowledgments.
Preface to the First Edition (Peter M. Roye and Beat Steinmann).
Contributors.
Introduction: Research on Collagen in the Author's Labortory, 1952-1982 (Karl A. Piez).
Heritable Disorders of Connective Tissue: A Personal Account of the Origins, Evolution, Validation, and Expansion of a Concept (Victor A. McKusick).
BIOLOGY OF EXTRACELLULAR MATRIX.
Morphology and Chemical Composition of Connective Tissue.
Collagen.
Elastin and the Microfibrillar Apparatus (Joel Rosenbloom and William R. Abrams).
Glycoslated Matrix Proteins (Dick Heineg et al.).
Adhesive Glycoproteins (Klaus von der Mark and Lydia Sorokin).
Keratins (E. Birgitte Lane).
Extracellular Matrix Degradation (Gillian Murphy and John J. Reynolds).
HERITABLE DISORDERS OF CONNECTIVE TISSUE.
Osteogenesis Imperfecta (Peter H. Byers and William G. Cole).
The Ehlers-Danlos Syndrome (Beat Steinmann, et al.).
Cutis Laxa and Premature Aging Syndromes (Jeffrey M. Davidson and MariaGabriella Giro).
Pseudoxanthoma Elasticum (Kenneth H. Neldner and Berthold Struk).
The Marfan Syndrome and Other Microfibrillar Disorders (Reed E. Pyeritz and Harry C. Dietz).
The Homocystinurias (Flemming Skovby and Jan P. Kraus).
Menkes Disease and the Occipital Horn Syndrome (Nina Horn and Zeynep Tümer).
Epidermolysis Bullosa (Leena Bruckner-Tuderman).
Prolidase Deficiency (Peter M. Royce and Beat Steinmann).
1-Antitrypsin Deficiency (Diane Wilson Cox).
Heritable Forms of Rickets and Osteomalacia (Michael P. Whyte).
Osteopetrosis (Michael P. Whyte).
Alkaptonuria (Bert N. La Du).
Fibrodysplasia Ossificans Progressiva (Frederick S. Kaplan, et al.).
Disorders of Lysosomal Enzymes.
Skeletal Dysplasias.
Disorders of Keratinization (Meral J. Arin, et al.).
Alport Syndrome (Karl Tryggvason and Paula Martin).
Miscellaneous Disorders.
Appendix I: International Nomenclature of Constitutional Disorders of Bone: Osteochondrodysplasias.
Appendix II: Extracellular Matrix Metabolites in Body Fluids (Leila Risteli and Juha Risteli).
Index.