Fibrocystic Diseases of the Liver [recurso electrónico] / edited by Karen F. Murray, Anne M. Larson.

Por: Murray, Karen F [editor.]Colaborador(es): Larson, Anne M [editor.] | SpringerLink (Online service)Tipo de material: TextoTextoSeries Clinical GastroenterologyEditor: Totowa, NJ : Humana Press, 2010Descripción: XII, 640p. 161 illus., 70 illus. in color. online resourceTipo de contenido: text Tipo de medio: computer Tipo de portador: online resourceISBN: 9781603275248Tema(s): Medicine | Gastroenterology | Clinical medicine | Nephrology | Pediatrics | Abdomen -- Surgery | Medicine & Public Health | Gastroenterology | Hepatology | Nephrology | Pediatrics | Abdominal SurgeryFormatos físicos adicionales: Printed edition:: Sin títuloClasificación CDD: 616.33 Clasificación LoC:RC799-869Recursos en línea: Libro electrónicoTexto
Contenidos:
Pathophysiology and Development -- Embryology and Development of the Ductal Plate -- Cholangiocyte Biology as Relevant to Cystic Liver Diseases -- Cholangiocyte Cilia and Basal Bodies -- Genetics of Fibrocystic Diseases of the Liver and Molecular Approaches to Therapy -- Diagnosis -- Radiologic Findings in the Fibrocystic Diseases -- Pathology of Fibrocystic Diseases of the Liver -- Disease States -- Alagille Syndrome and JAGGED1/NOTCH Sequence -- Biliary Atresia and the Ductal Plate -- Nephronophthisis and Renal–Hepatic–Pancreatic Dysplasia of Ivemark -- Meckel and Joubert Syndromes -- Bardet–Biedl and Jeune Syndromes -- Congenital Disorders of Glycosylation and Their Effects on the Liver -- Autosomal Recessive Polycystic Kidney Disease -- Caroli Disease, Caroli Syndrome, and Congenital Hepatic Fibrosis -- Simple Hepatic Cysts/Choledochal Cysts -- Autosomal Dominant Polycystic Liver Disease -- Echinococcal/Hydatid Cysts of the Liver -- Miscellaneous Cystic Lesions of the Liver -- Complications -- Vascular Complications of Fibrocystic Liver Disease -- Biliary Cystadenoma and Cystadenocarcinoma -- Cholangitis -- Surgical Management -- Surgical Management of Fibrocystic Liver Disease.
En: Springer eBooksResumen: In recent years there have been huge advances in the understanding of the genetic and molecular basis of the fibrocystic diseases. This volume provides a thorough review of fibrocyctic diseases that affect the liver. It contains in-depth discussions of the genetics, molecular biology, pathogenesis, histology, clinical presentations, complications of, treatment, and prognosis of the conditions affecting children and adults, and hence will be the gold-standard reference for these conditions. In addition, the histological features that distinguish these conditions from other potentially fibrosing hepatopathies are illustrated. Conditions with syndromic features involving the kidney or other organ systems are also reviewed. Thorough review of the clinical phenotypes, their presentations, treatment, potential complications of, and prognosis is discussed. Fibrocystic Diseases of the Liver will be an invaluable resource for hepatologists, gastroenterologists, nephrologists, and hepatic surgeons who care for children and adults with liver disease, as well as basic scientists in molecular genetics, hepatobiliary pathophysiology, hepatology and nephrology.
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Existencias
Tipo de ítem Biblioteca actual Colección Signatura Copia número Estado Fecha de vencimiento Código de barras
Libro Electrónico Biblioteca Electrónica
Colección de Libros Electrónicos RC799 -869 (Browse shelf(Abre debajo)) 1 No para préstamo 372542-2001

Pathophysiology and Development -- Embryology and Development of the Ductal Plate -- Cholangiocyte Biology as Relevant to Cystic Liver Diseases -- Cholangiocyte Cilia and Basal Bodies -- Genetics of Fibrocystic Diseases of the Liver and Molecular Approaches to Therapy -- Diagnosis -- Radiologic Findings in the Fibrocystic Diseases -- Pathology of Fibrocystic Diseases of the Liver -- Disease States -- Alagille Syndrome and JAGGED1/NOTCH Sequence -- Biliary Atresia and the Ductal Plate -- Nephronophthisis and Renal–Hepatic–Pancreatic Dysplasia of Ivemark -- Meckel and Joubert Syndromes -- Bardet–Biedl and Jeune Syndromes -- Congenital Disorders of Glycosylation and Their Effects on the Liver -- Autosomal Recessive Polycystic Kidney Disease -- Caroli Disease, Caroli Syndrome, and Congenital Hepatic Fibrosis -- Simple Hepatic Cysts/Choledochal Cysts -- Autosomal Dominant Polycystic Liver Disease -- Echinococcal/Hydatid Cysts of the Liver -- Miscellaneous Cystic Lesions of the Liver -- Complications -- Vascular Complications of Fibrocystic Liver Disease -- Biliary Cystadenoma and Cystadenocarcinoma -- Cholangitis -- Surgical Management -- Surgical Management of Fibrocystic Liver Disease.

In recent years there have been huge advances in the understanding of the genetic and molecular basis of the fibrocystic diseases. This volume provides a thorough review of fibrocyctic diseases that affect the liver. It contains in-depth discussions of the genetics, molecular biology, pathogenesis, histology, clinical presentations, complications of, treatment, and prognosis of the conditions affecting children and adults, and hence will be the gold-standard reference for these conditions. In addition, the histological features that distinguish these conditions from other potentially fibrosing hepatopathies are illustrated. Conditions with syndromic features involving the kidney or other organ systems are also reviewed. Thorough review of the clinical phenotypes, their presentations, treatment, potential complications of, and prognosis is discussed. Fibrocystic Diseases of the Liver will be an invaluable resource for hepatologists, gastroenterologists, nephrologists, and hepatic surgeons who care for children and adults with liver disease, as well as basic scientists in molecular genetics, hepatobiliary pathophysiology, hepatology and nephrology.

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