Event Videos
http://www.ncbi.nlm.nih.gov/pubmed/24863185 Della Corte C, Nobili V, Comparcola D, Cainelli F, Vento S. Management of chronic hepatitis B in children: an unresolved issue. J Gastroenterol Hepatol. 2014 May; 29(5): 912-9. Published on:
May-2014
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http://www.ncbi.nlm.nih.gov/pubmed/24659442 Mustafa Aydin1, Ugur Deveci1, Nilay Hakan2, Sukran Ozdiller1 and Feyza Girgin1 Published on:
Mar-2014
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http://www.ncbi.nlm.nih.gov/pubmed/24122953 Pugliese R, Fonseca EA, Porta G, Danesi V, Guimaraes T, Porta A, Miura IK, Borges C, Candido H, Benavides M, Feier FH, Godoy A, Cardoso RA, Kondo M, Chapchap P, Neto JS. Ascites and serum sodium are markers of increased waiting list mortality in children with chronic liver failure. Hepatology. 2014 May; 59(5):1964-71. Published on:
Jun-2014
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What is Hepatitis A?Hepatitis A is an infection of the liver caused by a virus called Hepatitis A virus. How does this disease spread?Hepatitis A is an enterally transmitted disease that is it is food borne. It spreads from one to another through contaminated food or water. |
Naim Alkhouri, Sana Mansoor, Paola Giammaria, Rocio Lopez, Valerio Nobili, Background: Noninvasive hepatic fibrosis scores that predict the presence of advanced fibrosis have been developed and validated in adult patients with NAFLD. There is an urgent need to test and develop similar scores in children with NAFLD. The aim of our study was to assess the utility of commonly used adult fibrosis scores in pediatric NAFLD and to develop a pediatric specific fibrosis score that can predict advanced fibrosis. Methods: Published on:
May-2014
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FDA and EMA Join Forces on Treatment of Gaucher Disease in Children FDA and the European Medicines Agency (EMA) released a draft joint proposal to facilitate research in the development of new drugs to treat Gaucher disease in children. The proposal, the result of consultation with various groups of stakeholders, facilitates an agreement between an FDA Pediatric Study Plan and an EMA Paediatric Investigation Plan and addresses the development of drugs for rare diseases in a reduced timeframe in a limited number of patients. |
http://www.ncbi.nlm.nih.gov/pubmed/24732866 Muir AJ. The rapid evolution of treatment strategies for hepatitis C. Am J Gastroenterol. 2014 May; 109(5):628-35. Abstract Hepatitis C virus (HCV) treatment took a major step forward at the end of 2013 with the approvals of the second-generation protease inhibitor Simeprevir (Olysio) and the nucleotide polymerase inhibitor Sofosbuvir (Sovaldi). The interferon-free regimen of Sofosbuvir and ribavirin is now available for genotype 2 and 3 patients. This regimen for 12 weeks is highly effective for genotype 2, whereas genotype 3 has proven to be more challenging and requires 24 weeks of therapy. Genotype 1 patients have reduced exposure to peginterferon-α with a 12-week regimen with sofosbuvir and a 24-week regimen with Simeprevir. Published on:
Jun-2014
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http://www.ncbi.nlm.nih.gov/pubmed/24659442 Abstract OBJECTIVE: METHODS: Published on:
Jan-2014
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KOLKATA: Kids, beware. The next time you gorge on junk food, keep in mind that those burgers and rolls are pushing you to a point of no return. |