Pediatric Liver Disease: Hepatology, cartea 5
Editat de M. M. Fisheren Limba Engleză Paperback – 27 mai 2012
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Specificații
ISBN-13: 9781468443875
ISBN-10: 1468443879
Pagini: 308
Ilustrații: IX, 296 p. 45 illus.
Dimensiuni: 178 x 254 x 16 mm
Greutate: 0.54 kg
Ediția:Softcover reprint of the original 1st ed. 1983
Editura: Springer Us
Colecția Springer
Seria Hepatology
Locul publicării:New York, NY, United States
ISBN-10: 1468443879
Pagini: 308
Ilustrații: IX, 296 p. 45 illus.
Dimensiuni: 178 x 254 x 16 mm
Greutate: 0.54 kg
Ediția:Softcover reprint of the original 1st ed. 1983
Editura: Springer Us
Colecția Springer
Seria Hepatology
Locul publicării:New York, NY, United States
Public țintă
ResearchCuprins
Developmental Aspects of Liver Structure And Function.- Early Development of the Liver: a Review.- Developmental Aspects of the Hepatic Circulation.- Discussion.- Developmental Aspects of Bile Acid Metabolism and Hepatic Function.- Hepatic Drug-Metabolizing Enzymes during Embryonic and Fetal Development.- Discussion.- Cholestatic Liver Disease in Newborns and Infants.- A Clinical Approach to Cryptogenic Cholestasis of the Newborn.- Role of Bile Acids in Pediatric Cholestasis.- Microfilament Dysfunction in Cholestasis: Possible Involvement in Familial Pediatric Cholestatic Syndromes.- Discussion.- Extrahepatic Biliary Atresia: Clinical Aspects.- Pathology and Pathogenesis of Extrahepatic Biliary Atresia.- The Surgery of Biliary Atresia: Current Investigations.- Discussion.- New Developments in Viral Hepatitis.- Viral Hepatitis Type A: Redefinition of Virologie, Clinical and Epidemiologic Features.- Discussion.- Viral Hepatitis, Type B.- Hepatitis Non A Non B: A Newly Recognized Old Disease.- Discussion.- Metabolic Liver Disease.- Hereditary Fructose Intolerance.- Deficiency of Fumarylacetoacetase in the Acute Form of Hereditary Tyrosinemia with Reference to Prenatal Diagnosis.- A Metabolic Basis for Treatment of Type I Glycogen Storage Disease.- Discussion.- Wilson’s Disease — Hepatolenticular Degeneration. The Importance of Early Diagnosis.- Alpha-1-Antitrypsin Deficiency.- Discussion.- Closing Remarks.- Contributors.