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Hemochromatosis: Genetics, Pathophysiology, Diagnosis and Treatment (Hardcover)

James C. Barton

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ISBN 10: 0521593808 / ISBN 13: 9780521593809
Nuevos Condición: New Encuadernación de tapa dura
Librería: AussieBookSeller (SILVERWATER, NSW, Australia)

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Descripción

Hardcover. Once thought rare, hemochromatosis is now acknowledged as one of the commonest inherited disorders, affecting one in two hundred people of western Caucasian descent. It is est.Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability. 616 pages. 2.449. N° de ref. de la librería 9780521593809

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Detalles bibliográficos

Título: Hemochromatosis: Genetics, Pathophysiology, ...

Año de publicación: 2000

Encuadernación: Hardcover

Condición del libro:New

Edición: 1st.

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Sinopsis:

Once considered a rare condition, hemochromatosis is now acknowledged as one of the commonest inherited disorders, affecting one in two hundred people of Western Caucasian descent and in the U.S. alone, over one million people. This is the most comprehensive clinical reference yet on hemochromatosis. The international team of 94 authors from twelve countries includes specialists in internal medicine, hematology, hepatology, genetics, biochemistry, and molecular biology. In 57 in-depth chapters they cover all aspects of pathophysiology, epidemiology, diagnosis and treatment. The text thoroughly explains the latest developments in the genetics of the disorder, including sections on screening, diagnostic techniques, and clinical complications. In addition, chapters consider social and ethical issues. With over 200 illustrations--including 40 color plates--this is today's definitive resource for all clinicians involved in the management of hemochromatosis, and for scientists interested in iron metabolism and iron overload.

Book Description:

This is the most comprehensive clinical reference yet on hemochromatosis, now acknowledged as one of the commonest inherited disorders, affecting one in two hundred people of western Caucasian descent. The international author team cover all aspects of pathophysiology, epidemiology, diagnosis and treatment, and the latest developments in the genetics of the disorder are well explained. Highly illustrated, up-to-date and authoritative, this is the definitive resource for all clinicians involved in the management of hemochromatosis, and will also be invaluable to scientists interested in iron metabolism and iron overload.

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