000 04039nam a22005295i 4500
001 u372542
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005 20160812084103.0
007 cr nn 008mamaa
008 100721s2010 xxu| s |||| 0|eng d
020 _a9781603275248
_9978-1-60327-524-8
040 _cMX-MeUAM
050 4 _aRC799-869
082 0 4 _a616.33
_223
100 1 _aMurray, Karen F.
_eeditor.
245 1 0 _aFibrocystic Diseases of the Liver
_h[recurso electrónico] /
_cedited by Karen F. Murray, Anne M. Larson.
264 1 _aTotowa, NJ :
_bHumana Press,
_c2010.
300 _aXII, 640p. 161 illus., 70 illus. in color.
_bonline resource.
336 _atext
_btxt
_2rdacontent
337 _acomputer
_bc
_2rdamedia
338 _aonline resource
_bcr
_2rdacarrier
347 _atext file
_bPDF
_2rda
490 1 _aClinical Gastroenterology
505 0 _aPathophysiology 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.
520 _aIn 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.
650 0 _aMedicine.
650 0 _aGastroenterology.
650 0 _aClinical medicine.
650 0 _aNephrology.
650 0 _aPediatrics.
650 0 _aAbdomen
_xSurgery.
650 1 4 _aMedicine & Public Health.
650 2 4 _aGastroenterology.
650 2 4 _aHepatology.
650 2 4 _aNephrology.
650 2 4 _aPediatrics.
650 2 4 _aAbdominal Surgery.
700 1 _aLarson, Anne M.
_eeditor.
710 2 _aSpringerLink (Online service)
773 0 _tSpringer eBooks
776 0 8 _iPrinted edition:
_z9781603275231
830 0 _aClinical Gastroenterology
856 4 0 _zLibro electrónico
_uhttp://148.231.10.114:2048/login?url=http://link.springer.com/book/10.1007/978-1-60327-524-8
596 _a19
942 _cLIBRO_ELEC
999 _c200422
_d200422