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nio masaki (curatore) - introduction to biliary atresia

Introduction to Biliary Atresia




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Dettagli

Genere:Libro
Lingua: Inglese
Editore:

Springer

Pubblicazione: 07/2021
Edizione: 1st ed. 2021





Trama

This book offers a comprehensive overview of the latest standard medical procedures and surgical techniques for biliary atresia (BA), as well as the perioperative care, long-term follow-up and transitions. Experts on pediatrics in such fields as hepatology, surgery, pathology, and liver transplantation present their research findings and analyses of this rare and intractable disease of unknown etiology. In Japan, shared experience and sound understanding based on conferences and guidelines have led to standardization of management and clinical care and, as a result, better outcomes.

Providing insights into improving surgical outcomes, and including special chapters focusing on social support systems for patients and families as well as recent advances in early diagnosis, this book a valuable resource for medical professionals around the globe who are involved in treating biliary atresia. It is especially useful for pediatric hepatologists, pediatric surgeons and transplant surgeons.






Sommario

Biliary Atresia: A Historical Overview
History of The Japanese Biliary Atresia Society (JABS)
Japanese Biliary Atresia Registry (JBAR)
Pathogenesis: Overview
Pathogenesis: Genetics/Epigenetics
Pathogenesis: Viral Infection
Pathogenesis: Maternal Microchimerism
Epidemiology: Incidence and Gender Ratio
Epidemiology: Ethnic Variations/Family Histories/Heredity
Epidemiology: Gestational Age/Birth Weight /Associated Anomalies
Classifications
Mass Screening
Stool Color Card System
Prenatal Diagnosis and Signs/Symptoms
Intracranial Hemorrhage
Pathology
Biomarkers 
Differential Diagnosis
Diagnostic Modalities
Preoperative Management and Direct Cholangiography
Operative Procedures: Open Kasai Procedure
Operative Procedures: Laparoscopic Kasai Procedure
Operative Procedures: Re-do Kasai Procedure
Operative Procedures: Cadaveric Liver Transplantation
Operative Procedures: Living Donor Liver Transplantation
Medical Treatment: UDCA/Steroid
Medical Treatment: Kampo Medicine
Prevention/Treatment of Postoperative Cholangitis
Nutritional Support
Protocols of Follow-up Management
Prognostic Indicators
Long-term Complications: Gastro-Esophageal Varices
Long-term Complications: Hypersplenism
Long-term Complications: Cholangitis/Gall Stones
Long-term Complications: Hepatopulmonary Syndrome
Long-term Complications: Portopulmonary Hypertension
Long-term Complications: Liver Cirrhosis/Hepatic Encephalopathy 
Long-Term Results, General
Long-Term Results, Deformity of Intrahepatic Bile Ducts
Long-Term Results, Social Performance
Long-Term Results, Liver Transplantation
Biliary Atresia and Pregnancy/Delivery
Biliary Atresia and Malignancy
Future Prospects
Transition in Biliary Atresia
Society of Patients and Families
Clinical Guidelines for Biliary Atresia




Autore

Masaki Nio, M.D., Ph.D., ACSF

Masaki Nio is Professor and Chief of Pediatric Surgery at Tohoku University Graduate School of Medicine and Director of Pediatric Medical Center of Tohoku University Hospital. In 1981, he completed a M.D. course at Tohoku University School of Medicine. In 1983, he joined the Second Department of Surgery, Tohoku University Hospital, which Professor Morio Kasai presided over from 1963 to 1986. In 1987, he completed a Ph.D. course in Pediatric Surgery at Tohoku University Graduate School of Medicine. From 1991 to 1993, he worked as a research fellow in Children’s Hospital of Los Angeles, USA. He served as the President of Japanese Society of Pediatric Surgeons, a Board Member of Japan Surgical Society, a Board Member of Pacific Association of Pediatric Surgeons, the Chairman of Japanese Biliary Atresia Society, and so on. He has been a secretary general of Japanese Biliary Atresia Society since 2008.











Altre Informazioni

ISBN:

9789811621598

Condizione: Nuovo
Dimensioni: 279 x 210 mm Ø 1281 gr
Formato: Copertina rigida
Illustration Notes:XI, 350 p. 181 illus., 142 illus. in color.
Pagine Arabe: 350
Pagine Romane: xi


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