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intrahepatic वाक्य

"intrahepatic" हिंदी मेंintrahepatic in a sentence
उदाहरण वाक्यमोबाइल
  • Genetic mutations affecting hepatic bile salt transport molecules have also been found in patients with progressive familial intrahepatic cholestasis ( PFIC ).
  • Methods of treating the portal hypertension include : transjugular intrahepatic portosystemic shunt, or a distal splenorenal shunt procedure or a liver transplantation.
  • High levels of alpha-fetoprotein ( AFP ) in the blood can be found in many cases of HCC and intrahepatic cholangiocarcinoma.
  • Septal fibrosis and pseudolobules, inflammatory infiltrates, signs of cholestasis, and reduced numbers of intrahepatic bile ducts progresses to live cirrhosis.
  • The corresponding protein in mice is essential for the development of B cells and red blood cells, and for the prevention of intrahepatic cholestasis.
  • Often testing will be done to exclude more common conditions that present in a similar fashion, including intrahepatic cholestasis of pregnancy, and autoimmune hepatitis.
  • Researchers have found many infants with neonatal intrahepatic cholestasis have the same mutations in the " SLC25A13 " gene as adults with type II citrullinemia.
  • Transjugular intrahepatic portosystemic shunt procedures, or TIPS involve decompressing the portal vein by shunting a portal venule to a lower pressure systemic venule, under guidance with fluoroscopy.
  • Intrahepatic vein fetal blood sampling may be done as an alternative to PUBS . It involves the needle being inserted into the intrahepatic part of the umbilical cord in the fetal abdomen.
  • Intrahepatic vein fetal blood sampling may be done as an alternative to PUBS . It involves the needle being inserted into the intrahepatic part of the umbilical cord in the fetal abdomen.
  • In clinical practice the pressure is not measured directly until the decision to take a liver biopsy for suspected cirrhosis ( chronic liver failure ), or to place a transjugular intrahepatic portosystemic shunt has been made.
  • If the ductus venosus fails to occlude after birth, it remains patent ( open ), and the individual is said to have a patent ductus venosus and thus an intrahepatic portosystemic shunt ( PSS ).
  • CXCL10 in plasma is mirrored by intrahepatic CXCL10 mRNA, and both strikingly predict the first days of elimination of HCV RNA (  first phase decline ) during interferon / ribavirin therapy for all HCV genotypes.
  • The rationale for this approach is that minute residual bile duct remnants may be present in the fibrous tissue of the porta hepatis and thus provide direct connection with the intrahepatic ductule system to allow bile drainage.
  • There are also many pediatric liver diseases, including biliary atresia, alpha-1 antitrypsin deficiency, alagille syndrome, progressive familial intrahepatic cholestasis, Langerhans cell histiocytosis and regenerate and has a large reserve capacity.
  • Discrete localized enlargements of normal structures ( ureters, blood vessels, intrahepatic or extrahepatic biliary ducts, pulmonary inclusions, or gastrointestinal duplications ) due to outflow obstructions or narrowings, or abnormal connections, may also present as a tumor.
  • The modified Sugiura procedure is indicated in patients with well-preserved liver function ( Child-Pugh class A or B without chronic ascites ) and who are not candidates for transjugular intrahepatic portosystemic shunt, distal splenorenal shunt, or liver transplantation
  • If the neonatal jaundice does not clear up with simple phototherapy, other causes such as biliary atresia, Progressive familial intrahepatic cholestasis, bile duct paucity, Alagille syndrome, alpha 1-antitrypsin deficiency, and other pediatric liver diseases should be considered.
  • Other liver-related complications ( portal hypertension, esophageal varices, ascites, hepatic encephalopathy ) are treated with the same modalities as used in cirrhosis, although the use of transjugular intrahepatic portosystemic shunt treatment is discouraged due to the lack of documented benefit.
  • Mutations in the IDH2 gene, along with mutations in the IDH1 gene, are also strongly correlated with the development of glioma, acute myeloid leukemia ( AML ), chondrosarcoma, intrahepatic cholangiocarcinoma ( ICC ), and angioimmunoblastic T-cell lymphoma cancers.
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