Hereditary Haemolytic Anaemias
Seiten
1989
Churchill Livingstone (Verlag)
978-0-443-08242-9 (ISBN)
Churchill Livingstone (Verlag)
978-0-443-08242-9 (ISBN)
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A monograph on congenital anaemias, combining aspects on laboratory diagnosis and clinical management. It discusses not only specific hereditary anaemias - their diagnosis, pathophysiology and therapy - but also the malarial hypothesis.
"The Hereditary Hemolytic Anemias", is a companion volume to "Acquired Immune Hermolytic Anemias". It examines the hereditary anemias individually, and as a group, with regard to their history, relationship to malaria, the diagnostic techniques used to study them, clinical features, pathophysiology, and therapy. An effort has been made to underscore the importance that the melding of basic science and clinical medicine has had in developing our understanding of these diseases. Hereditary anemias are usually first detected during infancy and childhood, but with more and more of even the more severely afflicted patients surviving to adulthood, contributors familiar with the manifestations of these diseases at all stages of life have been selected to provide articles for this book.
"The Hereditary Hemolytic Anemias", is a companion volume to "Acquired Immune Hermolytic Anemias". It examines the hereditary anemias individually, and as a group, with regard to their history, relationship to malaria, the diagnostic techniques used to study them, clinical features, pathophysiology, and therapy. An effort has been made to underscore the importance that the melding of basic science and clinical medicine has had in developing our understanding of these diseases. Hereditary anemias are usually first detected during infancy and childhood, but with more and more of even the more severely afflicted patients surviving to adulthood, contributors familiar with the manifestations of these diseases at all stages of life have been selected to provide articles for this book.
Introduction to hereditary haemolytica anaemia; congenital haemolytic anaemias - diagnostic strategy; the Thalassemia syndrome; sickling syndromes and unstable haemoglobin disease; disorders of the erythrocyte membrane; disorders of erythrocyte metabolism; haemolytic diseases of the newborn; mechanisms of red blood cell destruction in haemoltic anaemias; therapy of the hereditary haemolytic anaemias.
Zusatzinfo | 50 half-tones, 50 line drawings |
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Verlagsort | London |
Sprache | englisch |
Maße | 156 x 234 mm |
Gewicht | 1245 g |
Themenwelt | Medizinische Fachgebiete ► Innere Medizin ► Hämatologie |
Medizin / Pharmazie ► Medizinische Fachgebiete ► Pädiatrie | |
ISBN-10 | 0-443-08242-1 / 0443082421 |
ISBN-13 | 978-0-443-08242-9 / 9780443082429 |
Zustand | Neuware |
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