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Refinado por: assunto: Humans remover
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Prolonged Therapy of Advanced Chronic Hepatitis C with Low-Dose Peginterferon
Prolonged Therapy of Advanced Chronic Hepatitis C with Low-Dose Peginterferon
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Prolonged Therapy of Advanced Chronic Hepatitis C with Low-Dose Peginterferon

Di Bisceglie, Adrian M ; Shiffman, Mitchell L ; Everson, Gregory T ; Lindsay, Karen L ; Everhart, James E ; Wright, Elizabeth C ; Lee, William M ; Lok, Anna S ; Bonkovsky, Herbert L ; Morgan, Timothy R ; Ghany, Marc G ; Morishima, Chihiro ; Snow, Kristin K ; Dienstag, Jules L

The New England journal of medicine, 2008-12, Vol.359 (23), p.2429-2441 [Periódico revisado por pares]

Waltham, MA: Massachusetts Medical Society

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2
Sepsis in cirrhosis: report on the 7th meeting of the International Ascites Club
Sepsis in cirrhosis: report on the 7th meeting of the International Ascites Club
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Sepsis in cirrhosis: report on the 7th meeting of the International Ascites Club

Wong, F ; Bernardi, M ; Balk, R ; Christman, B ; Moreau, R ; Garcia-Tsao, G ; Patch, D ; Soriano, G ; Hoefs, J ; Navasa, M

Gut, 2005-05, Vol.54 (5), p.718-725 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd and British Society of Gastroenterology

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3
Mutations in NDUFAF3 (C3ORF60), Encoding an NDUFAF4 (C6ORF66)-Interacting Complex I Assembly Protein, Cause Fatal Neonatal Mitochondrial Disease
Mutations in NDUFAF3 (C3ORF60), Encoding an NDUFAF4 (C6ORF66)-Interacting Complex I Assembly Protein, Cause Fatal Neonatal Mitochondrial Disease
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Mutations in NDUFAF3 (C3ORF60), Encoding an NDUFAF4 (C6ORF66)-Interacting Complex I Assembly Protein, Cause Fatal Neonatal Mitochondrial Disease

Saada, Ann ; Vogel, Rutger O. ; Hoefs, Saskia J. ; van den Brand, Mariël A. ; Wessels, Hans J. ; Willems, Peter H. ; Venselaar, Hanka ; Shaag, Avraham ; Barghuti, Flora ; Reish, Orit ; Shohat, Mordechai ; Huynen, Martijn A. ; Smeitink, Jan A.M. ; van den Heuvel, Lambert P. ; Nijtmans, Leo G.

American journal of human genetics, 2009-06, Vol.84 (6), p.718-727 [Periódico revisado por pares]

Cambridge, MA: Elsevier Inc

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4
NDUFA2 Complex I Mutation Leads to Leigh Disease
NDUFA2 Complex I Mutation Leads to Leigh Disease
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NDUFA2 Complex I Mutation Leads to Leigh Disease

Hoefs, Saskia J.G. ; Dieteren, Cindy E.J. ; Distelmaier, Felix ; Janssen, Rolf J.R.J. ; Epplen, Andrea ; Swarts, Herman G.P. ; Forkink, Marleen ; Rodenburg, Richard J. ; Nijtmans, Leo G. ; Willems, Peter H. ; Smeitink, Jan A.M. ; van den Heuvel, Lambert P.

American journal of human genetics, 2008-06, Vol.82 (6), p.1306-1315 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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5
Quantitative tests of liver function measure hepatic improvement after sustained virological response: results from the HALT‐C trial
Quantitative tests of liver function measure hepatic improvement after sustained virological response: results from the HALT‐C trial
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Quantitative tests of liver function measure hepatic improvement after sustained virological response: results from the HALT‐C trial

EVERSON, G. T. ; SHIFFMAN, M. L. ; HOEFS, J. C. ; MORGAN, T. R. ; STERLING, R. K. ; WAGNER, D. A. ; DESANTO, J. L. ; CURTO, T. M. ; WRIGHT, E. C.

Alimentary pharmacology & therapeutics, 2009-03, Vol.29 (5), p.589-601 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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6
The spectrum of hepatic functional impairment in compensated chronic hepatitis C : results from the Hepatitis C Anti-viral Long-term Treatment against Cirrhosis Trial
The spectrum of hepatic functional impairment in compensated chronic hepatitis C : results from the Hepatitis C Anti-viral Long-term Treatment against Cirrhosis Trial
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The spectrum of hepatic functional impairment in compensated chronic hepatitis C : results from the Hepatitis C Anti-viral Long-term Treatment against Cirrhosis Trial

EVERSON, G. T ; SHIFFMAN, M. L ; MORGAN, T. R ; HOEFS, J. C ; STERLING, R. K ; WAGNER, D. A ; KULIG, C. C ; CURTO, T. M ; WRIGHT, E. C

Alimentary pharmacology & therapeutics, 2008-05, Vol.27 (9), p.798-809 [Periódico revisado por pares]

Oxford: Blackwell

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7
Portal‐systemic shunting in patients with fibrosis or cirrhosis due to chronic hepatitis C: the minimal model for measuring cholate clearances and shunt
Portal‐systemic shunting in patients with fibrosis or cirrhosis due to chronic hepatitis C: the minimal model for measuring cholate clearances and shunt
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Portal‐systemic shunting in patients with fibrosis or cirrhosis due to chronic hepatitis C: the minimal model for measuring cholate clearances and shunt

EVERSON, G. T. ; MARTUCCI, M. A. ; SHIFFMAN, M. L. ; STERLING, R. K. ; MORGAN, T. R. ; HOEFS, J. C.

Alimentary Pharmacology and Therapeutics, 2007-08, Vol.26 (3), p.401-410 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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8
A randomized, double-blind trial comparing pegylated interferon alfa-2b to interferon alfa-2b as initial treatment for chronic hepatitis C
A randomized, double-blind trial comparing pegylated interferon alfa-2b to interferon alfa-2b as initial treatment for chronic hepatitis C
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A randomized, double-blind trial comparing pegylated interferon alfa-2b to interferon alfa-2b as initial treatment for chronic hepatitis C

Lindsay, Karen L. ; Trepo, Christian ; Heintges, Tobias ; Shiffman, Mitchell L. ; Gordon, Stuart C. ; Hoefs, John C. ; Schiff, Eugene R. ; Goodman, Zachary D. ; Laughlin, Mark ; Yao, Ruji ; Albrecht, Janice K.

Hepatology (Baltimore, Md.), 2001-08, Vol.34 (2), p.395-403 [Periódico revisado por pares]

Philadelphia, PA: Elsevier Inc

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9
Novel mutations in the NDUFS1 gene cause low residual activities in human complex I deficiencies
Novel mutations in the NDUFS1 gene cause low residual activities in human complex I deficiencies
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Novel mutations in the NDUFS1 gene cause low residual activities in human complex I deficiencies

Hoefs, Saskia J.G. ; Skjeldal, Ola H. ; Rodenburg, Richard J. ; Nedregaard, Bård ; van Kaauwen, Edwin P.M. ; Spiekerkötter, Ute ; von Kleist-Retzow, Jürgen-Christoph ; Smeitink, Jan A.M. ; Nijtmans, Leo G. ; van den Heuvel, Lambert P.

Molecular genetics and metabolism, 2010-07, Vol.100 (3), p.251-256 [Periódico revisado por pares]

United States: Elsevier Inc

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10
Baculovirus complementation restores a novel NDUFAF2 mutation causing complex I deficiency
Baculovirus complementation restores a novel NDUFAF2 mutation causing complex I deficiency
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Baculovirus complementation restores a novel NDUFAF2 mutation causing complex I deficiency

Hoefs, Saskia J.G ; Dieteren, Cindy E.J ; Rodenburg, Richard J ; Naess, Karin ; Bruhn, Helene ; Wibom, Rolf ; Wagena, Esther ; Willems, Peter H ; Smeitink, Jan A.M ; Nijtmans, Leo G ; van den Heuvel, Lambert P

Human mutation, 2009-07, Vol.30 (7), p.E728-E736 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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