Category:Hepatology
From WikiMD's Food, Medicine & Wellnesspedia
Pages in category "Hepatology"
The following 200 pages are in this category, out of 297 total.
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- Abnormal liver function tests
- Accessory bile duct
- Aceruloplasminemia
- Acute hepatic failure
- Acute hepatitis
- Acute liver disease
- Acute liver failure
- Adenomyomatosis
- AFP-L3
- Alagille Syndrome
- Alagille syndrome
- Alanine aminotransferase
- Alpha-1 antitrypsin deficiency
- Anasarca
- Andrew Kenneth Burroughs
- Anorectal varices
- Anti-LKM antibody
- Anti-smooth muscle antibody
- Artificial extracorporeal liver support
- Artificial liver
- Asialoglycoprotein receptor 1
- ATC code A05
B
- Bancroft's sign
- Banti's syndrome
- Bare area of the liver
- Benign liver tumor
- Bile
- Bile acid
- Bile acids
- Bile canaliculus
- Bile duct carcinoma
- Bile ducts
- Bile salt sulfotransferase
- Biliary atresia
- Biliary disease
- Biliary microlithiasis
- Biliblanket
- Bilirubin diglucuronide
- Bilirubinuria
- Bioartificial liver device
- Boas' sign
- Bridging fibrosis
- Budd-Chiari syndrome
- Bulevirtide
C
- Canadian Journal of Gastroenterology and Hepatology
- Canal of hering
- Canals of Hering
- Cantlie line
- Caput medusae
- Carnitine palmitoyl transferase 1A deficiency
- Carnitine palmitoyltransferase 2 deficiency
- Caroli disease
- Central vein
- Charcot's cholangitis triad
- Child–Pugh score
- Cholangiocarcinoma
- Cholangitis
- Cholecystitis
- Choledochal cyst
- Cholelith
- Cholestatic pruritus
- Cholestyramine
- Choluria
- Chronic liver disease
- Chronic liver failure
- CIOMS/RUCAM scale
- Cirrhosis
- Cirrhosis of the liver
- Clinical Gastroenterology and Hepatology
- Clonorchiasis
- Colesevelam hydrochloride
- Common hepatic artery
- Congenital bile acid synthesis defect, type 1
- Congenital bile acid synthesis defect, type 2
- Councilman body
- COX20
- Crigler-Najjar syndrome
- Crigler–Najjar syndrome
- Cruveilhier–Baumgarten disease
D
E
F
G
- Gallstone
- Gallstones
- Gastric varices
- Gastrointestinal pathology
- Gilbert's syndrome
- Glycogen
- Glycogen storage disease
- Glycogen storage disease type 0, liver
- Glycogen storage disease type I
- Generalized gangliosidoses
- Glycogen storage disease type 2
- Glycogen storage disease type II
- Glycogen storage disease type 3
- Glycogenolysis
- Ground glass hepatocyte
- Gut (journal)
H
- Haemobilia
- Hangnail
- Hans Popper
- Hematoidin
- Hemolytic jaundice
- Hepatic
- Hepatic artery embolization
- Hepatic artery thrombosis
- Hepatic clearance
- Hepatic cystic hamartoma
- Hepatic diverticulum
- Hepatic encephalopathy
- Hepatic failure
- Hepatic ligaments
- Hepatic stellate cell
- Hepatic transplant
- Hepatic vein
- Hepatic veins
- Hepatic veno-occlusive disease
- Veno-occlusive disease
- Hepaticojejunostomy
- Hepatitis A
- Hepatitis a virus
- Hepatitis b core antibody
- Hepatitis B surface antigen
- Hepatitis F virus
- Hepato-biliary disorder
- Hepatoblastoma
- Hepatocellular adenoma
- Adult Primary Liver Cancer
- Childhood hepatocellular carcinoma
- Hepatocellular carcinoma
- Hepatocyte
- Hepatocyte growth factor
- Hepatoduodenal ligament
- Hepatogram
- Hepatokine
- Hepatolenticular degeneration
- Hepatolithiasis
- Hepatology
- Hepatoma
- Hepatoprotection
- Hepatotoxicity
- Hepatotoxins
- Hemochromatosis type 2
- HIDA scan
- Hormones of the liver
- Hydrocholeretic
I
L
- Left hepatic duct
- Lipolysis
- Lithocholic acid
- Liver cancer
- Liver cells
- Liver cirrhosis
- Liver cytology
- Liver dialysis
- Liver diseases
- Liver fibrosis
- Liver function
- Liver function test
- Liver Function Tests
- Liver function tests
- Liver kidney microsomal type 1 antibody
- Liver lobe
- Liver metastases
- Liver metastasis
- Liver regeneration
- Liver segment
- Liver sinusoid
- Liver sinusoidal endothelial cell
- Liver span
