SOEDAK2009 --- PREPARE FOR THE LONG RUN

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HBV genotype diversity in HIV/HBV co-infected patients in the Swiss HIV cohort
Florian Bihl1, Gladys Martinetti2, Bruno Ledergeber3, Sandrine Estoppey Younes4, Rainer Weber3, Pietro Vernazza5, Manuel Battegay6, Hans Jakob Furrer7,
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Switching to raltegravir in HIV-infected patients with well controlled viral load - efficacy and safety
Stefan Mauss1, Ana Milincovic2, Florian Berger1, Julia Henke1, Guenther Schmutz1, Petra Hegener1, Dieter Kuschak3, Stephan Schauseil3, Jospe Mallolas
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HIV integrase inhibition - more complex that simply blocking one key viral enzyme function
Séverine Louvel1, François Hamy2, Thomas KIimkait1
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New antiretroviral treatment options with integrase-inhibitors, CCR5-antagonists and second-generation-NNRTI and combination antiretroviral therapy (cART) in the ClinSurv cohort
Barbara Bartmeyer1, Kollan Christian1, Kühne Andrea1, Osamah Hamouda1, Studiengruppe Klinische Surveillance ClinSurv
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Final results from the Connect cohort confirm efficacy and safety of enfuvirtide in a "real life setting "
Olaf Degen1, Gerd Faetkenheuer2, J Bogner3, S Dupke4, S Koeppe5, S Gute6, W Becker7, A Tappe8, Egbert Wellmann8, Hans-Juergen Stellbrink
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Treatment of HIV-infected patients with a HAART regimen containing Enfuvirtide and a “second generation” protease inhibitor
Thore Lorenzen1, Irene Walther1, Johannes R. Bogner2, Jan van Lunzen3, Christoph Schuler4, Gerd Fätkenheuer5, Peter Gute6, Carl-Knut Schewe7, Siegfr
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Opportunities to assessan optimized salvage regimen in HIV infected triple-class experienced patients by the expert advice system RADATA
Thore Lorenzen1, Irene Walther1, Peter Gute2, Johannes R. Bogner3, Stefan Mauss4, Matthias Stoll5, Heribert Knechten6, Jürgen Rockstroh7, Jan van L
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Maraviroc in clinical practice - 24 weeks data
Heribert Knechten1, Christian Höhn1, Robert Ehret1, Frank Wiesmann1, Martin Hower2, Stefan Scholten3, Anton Neuwirth4, Wolfgang Köthemann4, Pa
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Durable efficacy and safety of etravirine in treatment-experienced, HIV-1-infected patients: pooled Week-96 results from the phase-III DUET-1 and DUET-2 trials
J Vingerhoets1, B Woodfall1
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Safety and efficacy of tenofovir DF (TDF) in combination with 3TC and efavirenz (EFV) in antiretroviral-naïve patients through seven years
Isabel Cassetti1, Jose Valdez R. Madruga2, Arnaldo Etzel3, Jamal Muhamad A.H. Suleiman4, Britta Ranneberg5, Lijie Zhong6, Andrew Cheng6, Jeffrey Enejosa6,
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The 48-week efficacy and safety of switching to fixed dose efavirenz/emtricitabine/tenofovir DF in HIV-1-infected patients receiving HAART
Edwin De Jesus1, Anton Pozniak2, Markus Bickel3, Joel Gallant4, Jose Arribas5, Yun Zhou6, Andrew Cheng6, Jeffrey Enejosa6
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Simplification of therapy (ART) with Efavirenz/Emtricitabine/Tenofovir DF single tablet regimen vs. continued ART in suppressed, HIV-infected patients
B. Young1, E. de Jesus2, J.O. Morales-Ramirez3, Tina Nakonz4, J-F. Maa5, D. Seekins5, A. Farajallah5, R. Ebrahimi6, J. Flaherty6
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Safety and tolerability of etravirine (ETR) in hepatitis B and/or C co-infected patients in DUET-1 and 2: 48 week results
Albrecht Stoehr1, Gerd Fätkenheuer2, Klaus Göbels3, Frank-Detlef Goebel4, Hans Jäger5, Arend Moll6, Jürgen Kurt Rockstroh7, Dieter Schuster
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Langzeitverträglichkeit und -effizienz von Nevirapin als Bestandteil einer HAART
Ivanka Krznaric1, Stephan Dupke1
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Patient reported outcomes after simplification to a single tablet regimen of Efavirenz (EFV)/Emtricitabine (FTC)/Tenofovir DF (TDF)
S. Hodder1, K. Mounzer2, E. de Jesus3, Tina Nakonz4, K. Grimm5, A. Farajallah5, J. Flaherty6
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Safety and efficacy of tenofovir in pregnant women
Annette Elisabeth Haberl1, Richard Linde2, Anke Reitter3, Peter Gute4, Gaby Knecht4, Manfred Mösch5, Tessa Lennemann6, Gabriele Nisius6, Christoph
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Kivexa versus Truvada: similar virological outcomes in ART-naïve patients starting a lopinavir/ritonavir-based regimen. 48-week-data from the STAR and STELLA cohorts
Eva Wolf1, Axel Baumgarten2, Bernhard Bieniek3, Stefanie Holm4, Martin Hower5, Hans Jaeger6, Thomas Lutz7, Markus Mueller8, Wolfgang Schmidt9
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Efficacy and safety of TDF/FTC-containing first line HAART in clinical practice - two year data from the German outpatient cohort
Jan van Lunzen1, Gerd Fätkenheuer2, Thomas Lutz3, Stephan Klauke4, Stefan Mauss5, Carl Knud Schewe6, Heribert Knechten7, Patrick Braun7, Lothar Ga
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Gutes Ansprechen einer Kombinationstherapie von Trizivir/Tenofovir bei Vorbehandelten über 96 Wochen. CTP-Score vs.1.2 als prädiktives Tool für den Therapieerfolg
Stephan Dupke1, Bettina Hintsche1, Christoph Mayr1, Frank Schlote1, Arend Moll1, Felise Krauthausen1, Daniel Prziwara1, Dorothea Schleehauf1, Siegfried
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48-wk safety and efficacy of darunavir/ritonavir (DRV/r) in treatment-experienced children and adolescents in DELPHI
P Vis1, V Sekar1, B Van Baelen1, S Spinosa-Guzman1
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