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Epidermolysis Bullosa: Clinical, Epidemiologic and Laboratory Advances and the Findings of the National Epidermolysis Bullosa Registry - Hardcover

 
9780801860249: Epidermolysis Bullosa: Clinical, Epidemiologic and Laboratory Advances and the Findings of the National Epidermolysis Bullosa Registry

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Reseña del editor

Inherited epidermolysis bullosa (EB) is a group of rare genetic diseases in which the skin is mechanically very fragile, resulting in chronic blister formation. In the most severe cases, affected persons may also experience disease involvement of other organs, cancer, and even premature death. In this book, a distinguished group of medical authorities presents the first comprehensive examination of EB employing a large, well-characterized research study population and using the latest epidemiological and biostatistical research principles. Unique to this work is its assessment of more than two thousand patients with EB, the largest such sample likely ever to be assembled in the world.

In addition to state-of-the-art reviews on basic science aspects of this disease, the book contains all of the significant original data generated on behalf of the National EB Registry Project during its first ten years of existence (1986-95); none of these data have been previously published in another peer-reviewed forum. Also included are detailed tables that will prove of value to clinicians and scientists alike as they diagnose, study, or treat individuals or groups with inherited EB.

Among the topics discussed are molecular and cell biology, epidemiology, diagnosis, classification, medical and surgical treatments, and clinical outcomes. The book will be of particular interest to dermatologists, neonatologists, pediatricians, medical geneticists, internists, oncologists, and scientists who are directly involved in the evaluation or study of EB. Although EB is a relatively rare disease, its ability to affect nearly every organ system (in severe cases) makes it of potential interest to a wide variety of medical specialists.

Biografía del autor

Jo-David Fine, M.D., M.P.H., is a professor of dermatology at the School of Medicine and a clinical professor of epidemiology at the School of Public Health, University of North Carolina at Chapel Hill, and Principal Investigator and Project Head, National Epidermolysis Bullosa Registry, Chapel Hill, North Carolina. Eugene A. Bauer, M.D., is Vice President for Academic Affairs and Dean of the Stanford University School of Medicine. Joseph McGuire, M.D., is a professor of dermatology at Stanford University Medical Center. Alan Moshell, M.D., is Chief, Skin Disease Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health.

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National Epidermolysis Bullosa Registry
ISBN 10: 0801860245 ISBN 13: 9780801860249
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Hardcover. Zustand: Good. No Jacket. Former library book; Pages can have notes/highlighting. Spine may show signs of wear. ~ ThriftBooks: Read More, Spend Less 2.2. Bestandsnummer des Verkäufers G0801860245I3N10

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Fine, Jo-David; Bauer, Eugene A.; McGuire, Joseph; Moshell, Alan
ISBN 10: 0801860245 ISBN 13: 9780801860249
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Hardcover. Zustand: As New. No Jacket. First Edition. Brand New condition except for a stamp on the front flyleaf. The covers look great. The binding is tight. The interior pages are clean and unmarked. Electronic delivery tracking will be issued free of charge. Bestandsnummer des Verkäufers 05744

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