Výsledky vyhledávání - "Marina Pereira Collela"

Recurrent thrombosis in antiphospholipid syndrome may be associated with cardiovascular risk factors and inflammatory response

Autor: Marina Pereira Collela, Joyce Annichino-Bizzachi, Bruna M Mazetto, Erich Vinicius De Paula, Fernanda Andrade Orsi, Sabrina da Silva Saraiva, Isadora Custódio, Simone Appenzeller

Publikováno v: Thrombosis research. 136(6)

Introduction Antiphospholipid syndrome (APS) is a pro-thrombotic autoimmune disease that affects different vascular beds, with potential risk for recurrence. Systemic lupus erythematosus (SLE), specific autoantibodies profile and atherogenic disorder

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ad47015d774aa5579084262da05518c
https://pubmed.ncbi.nlm.nih.gov/26601900

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Long-term increased factor VIII levels are associated to interleukin-6 levels but not to post-thrombotic syndrome in patients with deep venous thrombosis

Autor: Marina Pereira Collela, Joyce M. Annichino-Bizzacchi, Fernanda Andrade Orsi, Bruna M Mazetto, Luis Fernando Bittar, Erich Vinicius De Paula

Publikováno v: Thrombosis research. 135(3)

Introduction Increased FVIII levels are a well established risk factor for deep venous thrombosis (DVT), whose etiopathogenesis is not yet well understood. In this study, we aimed to evaluate the possibility that inflammatory markers and post-thrombo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acdbbd49abce417613511a98d8153b7f
https://pubmed.ncbi.nlm.nih.gov/25575413

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SUSTAIN: A Multicenter, Randomized, Placebo-Controlled, Double-Blind, 12-Month Study to Assess Safety and Efficacy of SelG1 with or without Hydroxyurea Therapy in Sickle Cell Disease Patients with Sickle Cell-Related Pain Crises

Autor: Julie Kanter, Kenneth I. Ataga, Marina Pereira Collela, Sandra Fátima Menosi Gualandro, Russell P. Rother, Wally R. Smith, Troy H. Guthrie, Rodolfo D. Cançado, Darla K. Liles, Victor R. Gordeuk, Jonathan W. Stocker, Scott A. Rollins, Ofelia A. Alvarez, Abdullah Kutlar, Jennifer Knight-Madden, Joao Ricardo Friedrisch

Publikováno v: Blood. 128:1-1

Introduction: Acute painful episodes, frequently called sickle cell-related pain crises (SCPC), are a substantial cause of morbidity in sickle cell disease (SCD). Although hydroxyurea (HU) is known to decrease the frequency of SCPC in sickle cell ane

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::eac26024e11ac01f4d98694174c65011
https://doi.org/10.1182/blood.v128.22.1.1

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