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A practical, clinically-oriented handbook of iron overload
disorders giving a compact guide to normal iron metabolism,
iron-related pathobiology, and the diagnosis and management of
heritable and acquired iron overload disorders. Many of these
disorders were discovered and characterized only in the last
decade, and are unmentioned or inadequately described in most
texts. Written by clinicians for clinicians, this handbook
summarizes information on diverse iron overload conditions,
including their history, signs, symptoms, and 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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