Handbook of Iron Overload Disorders

Handbook of Iron Overload Disorders - by James C. Barton July
Table of contents

Written by clinicians for clinicians, this handbook summarizes information on diverse iron overload conditions, including their history, signs, symptoms, physical examination findings, genetics, genotype-phenotype correlations, pathophysiology, differential diagnosis and treatment. Most physicians, regardless of specialty, encounter patients with systemic or organ-specific iron overload conditions. This book contains essential information for practising adult and pediatric medical specialists in the fields of hematology, gastroenterology, hepatology, rheumatology, endocrinology, diabetology, neurology, oncology, dermatology and internal medicine.

Pathologists, pharmacologists, geneticists, genetic counselors and epidemiologists will also find substantial, up-to-date sections in this handbook that are pertinent to their respective fields of interest.

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This book has been cited by the following publications. This list is generated based on data provided by CrossRef. When should iron supplementation in dialysis patients be avoided, minimized or withdrawn? Journal of Diabetes Research, Vol. HFE gene mutations are not risk factors for iron overload in European hemodialysis patients. Rostoker, Guy and Vaziri, Nosratola D. Impact of iatrogenic iron overload on the course of hepatitis C in the dialysis population: A plea for caution.

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