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ﺑﺎﺯﮔﺸﺖ ﺑﻪ ﺻﻔﺤﻪ ﻗﺒﻠﯽ
خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده: 4 مورد
نسخه الکترونیک
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Alcoholic hepatitis: Clinical manifestations and diagnosis
Clinical manifestations and diagnosis of alcohol-associated fatty liver disease and cirrhosis
Hematologic complications of alcohol use
Liver transplantation for alcohol-associated liver disease
Management and prognosis of alcoholic hepatitis
Management of alcohol-associated steatosis and alcohol-associated cirrhosis
Pathogenesis of alcohol-associated liver disease
Approach to the adult patient with an incidental solid liver lesion
Clinical features and diagnosis of hepatocellular carcinoma
Contrast-enhanced ultrasound for the evaluation of liver lesions
Diagnosis and management of cystic lesions of the liver
Focal nodular hyperplasia
Hepatic hemangioma
Hepatocellular adenoma
Pyogenic liver abscess
Evaluation of the adult patient with hepatic granuloma
Approach to the patient with suspected iron overload
Arthritis and bone disease associated with hereditary hemochromatosis
Clinical manifestations and diagnosis of hereditary hemochromatosis
<i>HFE</i> and other hemochromatosis genes
Management and prognosis of hereditary hemochromatosis
Methods to determine hepatic iron content
Clinical features and diagnosis of hepatocellular carcinoma
Contrast-enhanced ultrasound for the evaluation of liver lesions
Epidemiology and risk factors for hepatocellular carcinoma
Liver transplantation for hepatocellular carcinoma
Localized hepatocellular carcinoma: Liver-directed therapies for nonsurgical candidates not eligible for local thermal ablation
Localized hepatocellular carcinoma: Liver-directed therapies for nonsurgical candidates who are eligible for local ablation
Management of potentially resectable hepatocellular carcinoma: Prognosis, role of neoadjuvant and adjuvant therapy, and posttreatment surveillance
Overview of treatment approaches for hepatocellular carcinoma
Staging and prognostic factors in hepatocellular carcinoma
Surgical resection of hepatocellular carcinoma
Surveillance for hepatocellular carcinoma in adults
Systemic treatment for advanced hepatocellular carcinoma
Acute fatty liver of pregnancy
Alcoholic hepatitis: Clinical manifestations and diagnosis
Budd-Chiari syndrome: Epidemiology, clinical manifestations, and diagnosis
Budd-Chiari syndrome: Management
Caroli disease
Cirrhosis in adults: Etiologies, clinical manifestations, and diagnosis
Clinical features and diagnosis of hepatocellular carcinoma
Clinical features and diagnosis of metabolic dysfunction-associated steatotic liver disease (nonalcoholic fatty liver disease) in adults
Clinical manifestations and diagnosis of alcohol-associated fatty liver disease and cirrhosis
Clinical manifestations and diagnosis of hereditary hemochromatosis
Clinical manifestations, diagnosis, and prognosis of primary biliary cholangitis
Congestive hepatopathy
Diagnosis and management of cystic lesions of the liver
Evaluation of the adult patient with hepatic granuloma
Extrapulmonary manifestations of alpha-1 antitrypsin deficiency
Gastrointestinal amyloidosis: Clinical manifestations, diagnosis, and management
Gaucher disease: Pathogenesis, clinical manifestations, and diagnosis
Hepatic sinusoidal obstruction syndrome (veno-occlusive disease) in adults
Hepatic sinusoidal obstruction syndrome (veno-occlusive disease) in children
Overview of inherited disorders of glucose and glycogen metabolism
Overview of the evaluation of hepatomegaly in adults
Peliosis hepatis
Wilson disease: Clinical manifestations, diagnosis, and natural history
Approach to liver biopsy
Interpretation of nontargeted liver biopsy findings in adults
Transjugular liver biopsy
Acute fatty liver of pregnancy
Approach to evaluating pregnant patients with elevated liver biochemical and function tests
HELLP syndrome (hemolysis, elevated liver enzymes, and low platelets)
Intrahepatic cholestasis of pregnancy
Nausea and vomiting of pregnancy: Clinical findings and evaluation
Overview of coincident acute hepatobiliary disease in pregnant women
Pregnancy in women with pre-existing chronic liver disease
Acetaminophen (paracetamol) poisoning in adults: Pathophysiology, presentation, and evaluation
Acute liver failure in adults: Etiology, clinical manifestations, and diagnosis
Acute liver failure in adults: Management and prognosis
Palliative care for patients with end-stage liver disease
Approach to the patient with abnormal liver tests
Classification and causes of jaundice or asymptomatic hyperbilirubinemia
Diagnostic approach to the adult with jaundice or asymptomatic hyperbilirubinemia
Enzymatic measures of hepatic cholestasis (alkaline phosphatase, 5'-nucleotidase, gamma-glutamyl transpeptidase)
Overview of liver biochemical tests
Tests of the liver's biosynthetic capacity (eg, albumin, coagulation factors, prothrombin time)
Tests of the liver's capacity to transport organic anions and metabolize drugs
Bilirubin metabolism
Clinical features and diagnosis of metabolic dysfunction-associated steatotic liver disease (nonalcoholic fatty liver disease) in adults
Crigler-Najjar syndrome
Cystic fibrosis: Hepatobiliary disease
Diagnostic approach to the adult with jaundice or asymptomatic hyperbilirubinemia
Extrapulmonary manifestations of alpha-1 antitrypsin deficiency
Gilbert syndrome
Glucose-6-phosphatase deficiency (glycogen storage disease I, von Gierke disease)
Glycogen branching enzyme deficiency (glycogen storage disease IV, Andersen disease)
Glycogen debrancher deficiency (glycogen storage disease III, Cori disease)
Inherited disorders associated with conjugated hyperbilirubinemia in adults
Liver glycogen synthase deficiency (glycogen storage disease 0)
Liver phosphorylase deficiency (glycogen storage disease VI, Hers disease)
Management of metabolic dysfunction-associated steatotic liver disease (nonalcoholic fatty liver disease) in adults
Metabolic dysfunction-associated steatotic liver disease in children and adolescents
Other disorders of glycogen metabolism: GLUT2 deficiency and aldolase A deficiency
Overview of inherited disorders of glucose and glycogen metabolism
Pathogenesis of metabolic dysfunction-associated steatotic liver disease (nonalcoholic fatty liver disease)
Phosphorylase b kinase deficiency
Porphyrias: Overview of classification and evaluation
Wilson disease: Clinical manifestations, diagnosis, and natural history
Wilson disease: Epidemiology and pathogenesis
Wilson disease: Management
Acute portal vein thrombosis in adults: Clinical manifestations, diagnosis, and management
Chronic portal vein thrombosis in adults: Clinical manifestations, diagnosis, and management
Epidemiology and pathogenesis of portal vein thrombosis in adults
Noncirrhotic portal hypertension
Portal hypertension in adults
Nutritional issues in adult patients with cirrhosis
Approach to the patient with postoperative jaundice
Clinical manifestations, diagnosis, and prognosis of primary biliary cholangitis
Evaluation and treatment of low bone mass in primary biliary cholangitis (primary biliary cirrhosis)
Hypercholesterolemia in primary biliary cholangitis (primary biliary cirrhosis)
Liver transplantation in primary biliary cholangitis
Overview of the management of primary biliary cholangitis
Pathogenesis of primary biliary cholangitis (primary biliary cirrhosis)
Pruritus associated with cholestasis
Drug-induced liver injury
Drugs and the liver: Metabolism and mechanisms of injury
Hepatotoxicity due to herbal medications and dietary supplements
Hepatotoxicity of chemotherapy and other cytotoxic agents
Nonselective NSAIDs: Overview of adverse effects
Hepatic ductopenia and vanishing bile duct syndrome in adults
Budd-Chiari syndrome: Epidemiology, clinical manifestations, and diagnosis
Budd-Chiari syndrome: Management
Congestive hepatopathy
Etiology of the Budd-Chiari syndrome
Hepatic manifestations of sickle cell disease
Hepatic sinusoidal obstruction syndrome (veno-occlusive disease) in adults
Hepatic sinusoidal obstruction syndrome (veno-occlusive disease) in children
Ischemic hepatitis, hepatic infarction, and ischemic cholangiopathy
Pathogenesis of liver injury in circulatory failure
Peliosis hepatis

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