M. Diago

ORCID: 0000-0002-8583-2433
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Research Areas
  • Hepatitis C virus research
  • Liver Disease Diagnosis and Treatment
  • Hepatitis B Virus Studies
  • Systemic Lupus Erythematosus Research
  • HIV/AIDS drug development and treatment
  • Liver Disease and Transplantation
  • Liver Diseases and Immunity
  • Chronic Lymphocytic Leukemia Research
  • Immunodeficiency and Autoimmune Disorders
  • Hepatitis Viruses Studies and Epidemiology
  • Diabetes and associated disorders
  • Diet, Metabolism, and Disease
  • Alcohol Consumption and Health Effects
  • Diet and metabolism studies
  • Monoclonal and Polyclonal Antibodies Research
  • HIV Research and Treatment
  • Genetic and Kidney Cyst Diseases
  • COVID-19 Clinical Research Studies
  • Pancreatitis Pathology and Treatment
  • Drug Transport and Resistance Mechanisms
  • Autoimmune Bullous Skin Diseases
  • Pediatric Hepatobiliary Diseases and Treatments
  • Immune Cell Function and Interaction
  • Viral Infections and Immunology Research
  • Gallbladder and Bile Duct Disorders

Universitat de València
2013-2025

Hospital General Universitario De Valencia
2015-2024

Hospital Quirón Torrevieja
2010-2017

Hospital Clínico Universitario de Valencia
2014-2017

Cornell University
2016

Valencia Catholic University Saint Vincent Martyr
2015

Instituto de Salud Carlos III
2015

Clínica Girona
2011-2014

Hospital Marina Baixa
2013

Kyushu University
2013

Treatment with peginterferon alfa-2a alone produces significantly higher sustained virologic responses than treatment interferon in patients chronic hepatitis C virus (HCV) infection. We compared the efficacy and safety of plus ribavirin, alfa-2b initial C.

10.1056/nejmoa020047 article EN New England Journal of Medicine 2002-09-25

Covalent attachment of a 40-kd branched-chain polyethylene glycol moiety to interferon alfa-2a results in compound (peginterferon alfa-2a) that has sustained absorption, slower rate clearance, and longer half-life than unmodified alfa-2a. We compared the clinical effects regimen peginterferon with those initial treatment patients chronic hepatitis C.

10.1056/nejm200012073432301 article EN New England Journal of Medicine 2000-12-07

Available treatments for hepatitis B e antigen (HBeAg)-negative chronic are associated with poor sustained responses. As a result, nucleoside and nucleotide analogues typically continued indefinitely, strategy the risk of resistance unknown long-term safety implications.We compared efficacy peginterferon alfa-2a (180 microg once weekly) plus placebo, lamivudine (100 mg daily), alone in 177, 179, 181 patients HBeAg-negative B, respectively. Patients were treated 48 weeks followed an...

10.1056/nejmoa040431 article EN New England Journal of Medicine 2004-09-15

In a trial of patients with hepatitis B e antigen (HBeAg)-negative chronic B, 24 week post-treatment biochemical and virological response rates peginterferon alpha-2a or without lamivudine were significantly higher than alone. The effect pre-treatment factors on responses was investigated.Multivariate analyses performed using available data from 518 treated lamivudine, A defined as alanine aminotransferase (ALT) normalisation virus (HBV) DNA level <20,000 copies/ml.In logistic regression...

10.1136/gut.2005.089722 article EN Gut 2006-11-25

Insulin resistance affects sustained virological response (SVR) in chronic hepatitis C. To know whether adding metformin to standard antiviral treatment improves SVR, we conducted a prospective, multicentered, randomized, double-blinded, placebo-controlled trial 19 Spanish hospitals, including 123 consecutive patients with genotype 1 C and insulin resistance. Patients were randomized receive either (arm A; n = 59) or placebo B; 64) addition peginterferon alfa-2a (180 microg/week) ribavirin...

10.1002/hep.23206 article EN Hepatology 2009-08-05
Man‐Fung Yuen Tarik Asselah Ira M. Jacobson Maurizia Rossana Brunetto Harry L.A. Janssen and 95 more Tetsuo Takehara Jin Hou Thomas N. Kakuda Tom Lambrecht Maria Beumont Ronald Kalmeijer Carine Guinard‐Azadian Cristiana Mayer John Jezorwski Thierry Verbinnen Oliver Lenz Umesh Shukla Michael Biermer Stefan Bourgeois Thomas Vanwolleghem Frederik Nevens Yves Horsmans Hans Van Vlierberghe Ana Catharina de Seixas Santos Nastri Marcus Lacerda Alnoor Ramji Brian Conway Carla S. Coffin Harry L.A. Janssen Scott Fung Stephen D. Shafran Jin Hou Jan Šperl Petr Urbánek Stanislav Plíšek Václav Hejda Didier Samuel Karine Lacombe Fabien Zoulim Dominique Guyader F. Raffi Tarik Asselah Marc Bourlière Marie‐Noëlle Hilleret Heiner Wedemeyer Julian Schulze zur Wiesch Kathrin Sprinzl Florian van Bömmel Gudrun Hilgard Michael Sabranski Keikawus Arastéh Henry LY Chan Man‐Fung Yuen Vincent Wai‐Sun Wong Maurizia Rossana Brunetto Gloria Taliani Pietro Andreoné Pietro Lampertico Masayuki Kurosaki Hiroshi Yatsuhashi Kei Fujiwara Tetsuo Takehara Tomokazu Kawaoka Yasuhiro Asahina Hirayuki Enomoto Kazuhisa Yabushita Kazuo Notsumata Koichi Takaguchi Naoto Kawabe Naoya Kato Koji Ogawa Tadashi Namisaki Yoshiyuki Suzuki Jung‐Hwan Yoon Sang Hoon Ahn Young‐Suk Lim Seung Woon Paik Kuang Kiat Kiew Rosmawati Mohamed Soek Siam Tan Yeong Yeh Lee Maria Hlebowicz Hanna Berak Jacek Gąsiorowski Waldemar Halota Ewa Janczewska Natalia Geyvandova Viacheslav Morozov А. А. Андреева Д. А. Гусев E. I. Bessonova М. Ф. Осипенко Svetlana Romanova Natalia Gankina Olga Sagalova Tatiana Stepanova Javier Crespo M. Diago Fernandez Inmaculada José Luís Calleja

10.1016/s2468-1253(23)00148-6 article EN ˜The œLancet. Gastroenterology & hepatology 2023-07-10

Background & AimsPatients with nonalcoholic fatty liver disease (NAFLD)/metabolic dysfunction-associated steatotic (MASLD) face multifaceted burden which includes impaired health-related quality of life (HRQL) and potential stigmatization. We aimed to assess the in patients NAFLD relationship between experience stigma HRQL.MethodsMembers Global NASH Council created a survey about NAFLD. Participants completed 35-item questionnaire Liver Disease Burden (LDB) (7 domains), 36-item CLDQ-NASH (6...

10.1016/j.jhepr.2024.101066 article EN cc-by-nc-nd JHEP Reports 2024-03-12

<b>Background:</b> Increased serum and intrahepatic interferon γ inducible protein 10 (IP-10) levels in patients with chronic hepatitis C (CHC) have been described. <b>Aim:</b> To analyse the possible association of IP-10 different outcomes to antiviral therapy. <b>Patients:</b> A total 137 CHC treated peginterferon plus ribavirin. <b>Methods:</b> Serum were determined by enzyme linked immunosorbent assay before therapy, after 12 weeks treatment, 24 cessation Variables significantly...

10.1136/gut.2005.074062 article EN Gut 2005-09-09
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