|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | Regression of cirrhosis during treatment with tenofovir disoproxil fumarate for chronic hepatitis B: a 5-year open-label follow-up study显示文摘 | Patrick Marcellin Edward Gane Maria Buti Nezam Afdhal William Sievert Ira M Jacobson Mary Kay Washington George Germanidis John F Flaherty Raul Aguilar Schall Jeffrey D Bornstein Kathryn M Kitrinos G Mani Subramanian John G McHutchison E Jenny Heathcote | 2012 | The Lancet2012，，： | 14 |
| 2 | Human serum facilitates hepatitis C virus infection,and neutralizing responses inversely correlate with viral replication kinetics at the acute phase of hepatitis C virus infection显示文摘 | Lavillette D Morice Y Germanidis G | 2005 | J Virol2005，79，10： | 1 |
| 3 | Regression of cirrhosis during treatment with tenofovir disoproxil fumarate for chronic hepatitis B: a 5-year open-label follow-up study显示文摘 | Patrick Marcellin Edward Gane Maria Buti Nezam Afdhal William Sievert Ira M Jacobson Mary Kay Washington George Germanidis John F Flaherty Raul Aguilar Schall Jeffrey D Bornstein Kathryn M Kitrinos G Mani Subramanian John G McHutchison E Jenny Heathcote | 2012 | The Lancet2012，，： | 1 |
| 4 | Human serum facilitates hepatitis C virus infection, and neutralizing responses inversely correlate with viral replication kinetics at the acute phase of hepatitis C virus infection显示文摘 | Lavillette D Morice Y Germanidis G | 2005 | J Virol2005，79，10： | 1 |
| 5 | Conservation of the conformation and positive charges of hepatitis C virus E2 envelope glycoprotein hypervariable region 1 points to a role in cell attachment 显示文摘 | Penin F Combet C Germanidis G | 2001 | J Virol2001，75，12： | 1 |
| 6 | TGF-βsignaling is activated in patients with chronic HBV infection and repressed by SMAD7 overexpression after successful antiviral treatment显示文摘 | Argentou N Germanidis G Hytiroglou P | 2016 | Inflamm Res2016，65，5： | 1 |
| 7 | Hepatitis B virus ki- netics under antiviral therapy sheds light on differences in hepatitis B e antigen positive and negative infections 显示文摘 | Ribeiro RM Germanidis G Powers KA | 2010 | J Infect Dis2010，202，9： | 1 |
| 8 | Regression of cirrhosis during treatment with tenofovir disoproxil fumarate for chronic hepatitis B: a 5-year open-label follow-up study显示文摘 | Patrick Marcellin Edward Gane Maria Buti Nezam Afdhal William Sievert Ira M Jacobson Mary Kay Washington George Germanidis John F Flaherty Raul Aguilar Schall Jeffrey D Bornstein Kathryn M Kitrinos G Mani Subramanian John G McHutchison E Jenny Heathcote | 2012 | The Lancet2012，，： | 1 |
| 9 | Human serum facilitates hepatitis C virus infection,and neutralizing responses inversely correlate with viral replication kinetics at the acute phase of hepatitis C virus infection显示文摘 | Lavillette D Morice Y Germanidis G | 2005 | J Virol2005，79，10： | 1 |
| 10 | Conservation of the conformation and positive charges of hepatitis C virus E2 envelope glycoprotein hypervariable region 1 points to a role in cell attachmen显示文摘 | Penin F Combet C Germanidis G F | | 0，，12： | 1 |
| 11 | Liver Foxp3 and PD1/PDL1 expression is down - regulated in chronic HBV hepatitis on maintained remission related to the degree of inflammation 显示文摘 | Germanidis G Argentou N Hytiroglou P | 2013 | Front Immunol2013，，4： | 1 |
| 12 | Evolution of the hepatitis C virus second envelope protein hypervariable region in chronically infected patients receiving alpha interferon therapy显示文摘 | Pawlotsky J M Germanidis G Frainais P O | 1999 | J Virol1999，73，3： | 1 |
| 13 | Evolution of the hepatitis C virus second envelope protein hypervariable region in chronically infected patients receiving alpha interferon therapy显示文摘 | Pawlotshy JM Germanidis G Frainais PO | 1999 | J Virol1999，73，8： | 1 |
| 14 | Interferon resistance of hepatitis C virus genotype 1 b: relationship to non-struc- tural 5A gene quasispecies mutations 显示文摘 | Pawlotsky JM Germanidis G Neumann AU | 1998 | J Virol1998，72，4： | 1 |
| 15 | Conservation of the conformation and positive charges of hepatitis C virus E2 envelope glycoprotein hypervariable region 1 points to a role in cellattachment 显示文摘 | Penin F Combet C Germanidis G | 2001 | J Virol2001，75，12： | 1 |
| 16 | Human serumfacilitates hepatitis C vims infection, and neutralizing responsesinversely correlate with viral replication kinetics at the acute; phaseof hepatitis C vims infection 显示文摘 | Lavillette D Morice Y Germanidis G | 2005 | J Virol2005，79，10： | 1 |
| 17 | Evolution of the hepatitis C virussecond envelope protein hypervariable region in chronically infected patients receivingalpha interferon therapy显示文摘 | Pawlotsky JM Germanidis G Frainais PO | 1999 | J Virol1999，73，8： | 1 |
| 18 | Human serum facilitates hepatitis C virus infection,and neutralizing responses inversely correlate with viral replication kinetics at the acute phase of hepatitis C virus infection显示文摘 | Lavillette D Morice Y Germanidis G | 2005 | J Viro2005，79，10： | 1 |
| 19 | Postprandial response of bone turnover markers in patients with Crohn's disease显示文摘AIM:To investigate the postprandial response of bone turnover markers in patients with Crohn’s disease(CD).METHODS:Fifty nine patients with CD aged 38±14years,and 45 healthy individuals matched for age and body mass index were included in the study.All participants underwent an oral glucose tolerance test(OGTT)after an overnight fast and serum levels of the bone resorption marker C-terminal crosslinking telopeptide of type?Ⅰ?collagen(CTX-Ⅰ)and the bone formation marker procollagen type?Ⅰ?N propeptide were measured.Activity of the disease was assessed by calculation of the Crohn’s disease activity index(CDAI).RESULTS:Serum CTX-I was significantly higher in patients compared to controls(CTX-I:453±21 pg/mL vs 365±25 pg/mL,P=0.008),and values were significantly correlated with the activity of the disease(r=0.435,P=0.001).Results from OGTT-induced suppression of CTX-I showed two different trends.Patients with more active disease(assessed as CDAI>150)had a more excessive suppression of CTX-I compared to controls(55%vs 43%P<0.001),while patients on remission(assessed as CDAI<150)demonstrated an attenuated CTX-I suppression(30%vs 43%P<0.001).In line with this,CTX-I suppression after oral glucose load was significantly correlated with the activity of the disease(r=0.913,P<0.001).CONCLUSION:The physiological skeletal response of postprandial suppression of bone resorption is maintained in patients with CD and is strongly dependent to the activity of the disease. | Ioannis Karatzoglou Maria P Yavropoulou Maria Pikilidou George Germanidis Evangelos Akriviadis Alexra Papazisi Michael Daniilidis Pantelis Zebekakis John G Yovos | 2014 | World Journal of Gastroenterology2014，20，28： | 0 |
您所在的机构暂未开通此部分的功能，请联系管理员