15 results on '"Rosendaal, Frits Richard"'
Search Results
2. Publisher Correction: Partitioned polygenic risk scores identify distinct types of metabolic dysfunction-associated steatotic liver disease
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Jamialahmadi, Oveis, De Vincentis, Antonio, Tavaglione, Federica, Malvestiti, Francesco, Li-Gao, Ruifang, Mancina, Rosellina M., Alvarez, Marcus, Gelev, Kyla, Maurotti, Samantha, Vespasiani-Gentilucci, Umberto, Rosendaal, Frits Richard, Kozlitina, Julia, Pajukanta, Päivi, Pattou, François, Valenti, Luca, and Romeo, Stefano
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- 2025
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3. Hypercoagulability and the risk of recurrence in young women with myocardial infarction or ischaemic stroke: a cohort study
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Maino, Alberto, Algra, Ale, Peyvandi, Flora, Rosendaal, Frits Richard, and Siegerink, Bob
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- 2019
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4. Assessing Sequence Similarity between FVIII-Derived B-Cell Epitopes and Pathogen-Derived B-Cell Epitopes and the Risk of Inhibitor Development in Patients with Severe Hemophilia a
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Hassan, Shermarke, primary, Baselli, Guido, additional, Palla, Roberta, additional, Rosendaal, Frits Richard, additional, and Peyvandi, Flora, additional
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- 2022
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5. Genetically predicted cortisol levels and risk of venous thromboembolism
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Allarai, Elias, Lee, Wei-Hsuan, Burgess, Stephen, Larsson, Susanna C., Lindstrom, Sara, Wang, Lu, Smith, Erin N., Gordon, William, Van Hylckama Vlieg, Astrid, De Andrade, Mariza, Brody, Jennifer A., Pattee, Jack W., Haessler, Jeffrey, Brumpton, Ben Michael, Chasman, Daniel I., Suchon, Pierre, Chen, Ming-Huei, Turman, Constance, Germain, Marine, Wiggins, Kerri L., Macdonald, James, Brækkan, Sigrid Kufaas, Armasu, Sebastian M., Pankratz, Nathan, Jackson, Rabecca D., Nielsen, Jonas B, Giulianini, Franco, Puurunen, Marja K., Ibrahim, Manal, Heckbert, Susan R., Bammler, Theo K., Frazer, Kelly A., Mccauley, Bryan M., Taylor, Kent, Pankow, James S., Reiner, Alexander P., Gabrielsen, Maiken Elvestad, Deleuze, Jean-Francois, O'Donnell, Chris J., Kim, Jihye, Mcknight, Barbara, Kraft, Peter, Hansen, John Bjarne, Rosendaal, Frits Richard, Heit, John A., Psaty, Bruce M., Tang, Weihong, Kooperberg, Charles, Hveem, Kristian, Ridker, Paul M., Morange, Pierre-Emmanuel, Johnson, Andrew D., Kabrhel, Christopher, Alexandretrégouët, David, Smith, Nicholas L., Allara, Elias [0000-0002-1634-8330], Burgess, Stephen [0000-0001-5365-8760], and Apollo - University of Cambridge Repository
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Medicine and health sciences ,Multidisciplinary ,Kardiologi ,Hydrocortisone ,Biology and life sciences ,FOS: Social sciences ,Venous Thromboembolism ,Mendelian Randomization Analysis ,Endocrinology and Diabetes ,Social sciences ,Risk Factors ,Endokrinologi och diabetes ,Humans ,Cardiac and Cardiovascular Systems ,Pulmonary Embolism ,Medical Genetics ,Medicinsk genetik ,Research Article - Abstract
Introduction In observational studies, venous thromboembolism (VTE) has been associated with Cushing’s syndrome and with persistent mental stress, two conditions associated with higher cortisol levels. However, it remains unknown whether high cortisol levels within the usual range are causally associated with VTE risk. We aimed to assess the association between plasma cortisol levels and VTE risk using Mendelian randomization. Methods Three genetic variants in the SERPINA1/SERPINA6 locus (rs12589136, rs11621961 and rs2749527) were used to proxy plasma cortisol. The associations of the cortisol-associated genetic variants with VTE were acquired from the INVENT (28 907 cases and 157 243 non-cases) and FinnGen (6913 cases and 169 986 non-cases) consortia. Corresponding data for VTE subtypes were available from the FinnGen consortium and UK Biobank. Two-sample Mendelian randomization analyses (inverse-variance weighted method) were performed. Results Genetic predisposition to higher plasma cortisol levels was associated with a reduced risk of VTE (odds ratio [OR] per one standard deviation increment 0.73, 95% confidence interval [CI] 0.62–0.87, p Conclusions This study provides evidence that genetically predicted plasma cortisol levels in the high end of the normal range are associated with a decreased risk of VTE and that this association may be mediated by blood pressure. This study has implications for the planning of observational studies of cortisol and VTE, suggesting that blood pressure traits should be measured and accounted for.
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- 2022
6. The Netherlands Epidemiology of Obesity (NEO) study: study design and data collection
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de Mutsert, Renée, den Heijer, Martin, Rabelink, Ton Johannes, Smit, Johannes Willem Adriaan, Romijn, Johannes Anthonius, Jukema, Johan Wouter, de Roos, Albert, Cobbaert, Christa Maria, Kloppenburg, Margreet, le Cessie, Saskia, Middeldorp, Saskia, and Rosendaal, Frits Richard
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- 2013
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7. Factor VIII Epitope Analysis Using a Random Peptide Phage-Display Library Approach in the Sippet Cohort
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Hassan, Shermarke, primary, Baselli, Guido, additional, Palm, Kaia, additional, Rosendaal, Frits Richard, additional, Palla, Roberta, additional, and Peyvandi, Flora, additional
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- 2021
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8. The usefulness of D-dimer as a predictive marker for mortality in patients with COVID-19 hospitalized during the first wave in Italy.
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Hassan, Shermarke, Ferrari, Barbara, Rossio, Raffaella, la Mura, Vincenzo, Artoni, Andrea, Gualtierotti, Roberta, Martinelli, Ida, Nobili, Alessandro, Bandera, Alessandra, Gori, Andrea, Blasi, Francesco, Monzani, Valter, Costantino, Giorgio, Harari, Sergio, Rosendaal, Frits Richard, and Peyvandi, Flora
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COVID-19 ,FIBRIN fragment D ,HOSPITAL mortality ,MEDICAL personnel ,THERAPEUTICS - Abstract
Background: The coronavirus disease 2019 (COVID-19) presents an urgent threat to global health. Identification of predictors of poor outcomes will assist medical staff in treatment and allocating limited healthcare resources. Aims: The primary aim was to study the value of D-dimer as a predictive marker for in-hospital mortality. Methods: This was a cohort study. The study population consisted of hospitalized patients (age >18 years), who were diagnosed with COVID-19 based on real-time PCR at 9 hospitals during the first COVID-19 wave in Lombardy, Italy (Feb-May 2020). The primary endpoint was in-hospital mortality. Information was obtained from patient records. Statistical analyses were performed using a Fine-Gray competing risk survival model. Model discrimination was assessed using Harrell's C-index and model calibration was assessed using a calibration plot. Results: Out of 1049 patients, 507 patients (46%) had evaluable data. Of these 507 patients, 96 died within 30 days. The cumulative incidence of in-hospital mortality within 30 days was 19% (95CI: 16%-23%), and the majority of deaths occurred within the first 10 days. A prediction model containing D-dimer as the only predictor had a C-index of 0.66 (95%CI: 0.61–0.71). Overall calibration of the model was very poor. The addition of D-dimer to a model containing age, sex and co-morbidities as predictors did not lead to any meaningful improvement in either the C-index or the calibration plot. Conclusion: The predictive value of D-dimer alone was moderate, and the addition of D-dimer to a simple model containing basic clinical characteristics did not lead to any improvement in model performance. [ABSTRACT FROM AUTHOR]
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- 2022
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9. Performance of a clinical risk prediction model for inhibitor formation in severe haemophilia A.
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Hassan, Shermarke, Palla, Roberta, Valsecchi, Carla, Garagiola, Isabella, El‐Beshlawy, Amal, Elalfy, Mohsen, Ramanan, Vijay, Eshghi, Peyman, Karimi, Mehran, Gouw, Samantha Claudia, Mannucci, Pier Mannuccio, Rosendaal, Frits Richard, and Peyvandi, Flora
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BLOOD coagulation factor VIII antibodies ,PREDICTION models ,BLOOD coagulation factor VIII ,HEMOPHILIA ,VON Willebrand disease ,FORECASTING - Abstract
Background: There is a need to identify patients with haemophilia who have a very low or high risk of developing inhibitors. These patients could be candidates for personalized treatment strategies. Aims: The aim of this study was to externally validate a previously published prediction model for inhibitor development and to develop a new prediction model that incorporates novel predictors. Methods: The population consisted of 251 previously untreated or minimally treated patients with severe haemophilia A enrolled in the SIPPET study. The outcome was inhibitor formation. Model discrimination was measured using the C‐statistic, and model calibration was assessed with a calibration plot. The new model was internally validated using bootstrap resampling. Results: Firstly, the previously published prediction model was validated. It consisted of three variables: family history of inhibitor development, F8 gene mutation and intensity of first treatment with factor VIII (FVIII). The C‐statistic was 0.53 (95% CI: 0.46–0.60), and calibration was limited. Furthermore, a new prediction model was developed that consisted of four predictors: F8 gene mutation, intensity of first treatment with FVIII, the presence of factor VIII non‐neutralizing antibodies before treatment initiation and lastly FVIII product type (recombinant vs. plasma‐derived). The C‐statistic was 0.66 (95 CI: 0.57–0.75), and calibration was moderate. Using a model cut‐off point of 10%, positive‐ and negative predictive values were 0.22 and 0.95, respectively. Conclusion: Performance of all prediction models was limited. However, the new model with all predictors may be useful for identifying a small number of patients with a low risk of inhibitor formation. [ABSTRACT FROM AUTHOR]
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- 2021
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10. Hypercoagulability and the risk of recurrence in young women with myocardial infarction or ischaemic stroke: a cohort study
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JC onderzoeksprogramma Cardiovasculaire Epidemiologie, ZL Cerebrovasculaire Ziekten Medisch, Cardiovasculaire Epi Team 6, Circulatory Health, Brain, Maino, Alberto, Algra, Ale, Peyvandi, Flora, Rosendaal, Frits Richard, Siegerink, Bob, JC onderzoeksprogramma Cardiovasculaire Epidemiologie, ZL Cerebrovasculaire Ziekten Medisch, Cardiovasculaire Epi Team 6, Circulatory Health, Brain, Maino, Alberto, Algra, Ale, Peyvandi, Flora, Rosendaal, Frits Richard, and Siegerink, Bob
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- 2019
11. IgG subclasses as biomarkers for persistence of factor VIII inhibitors in previously untreated patients with severe haemophilia A.
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Peyvandi, Flora, Miri, Syna, Bucciarelli, Paolo, Valsecchi, Carla, Schiavone, Lucia, Boscarino, Marco, Palla, Roberta, Mannucci, Pier Mannuccio, and Rosendaal, Frits Richard
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BLOOD coagulation factor VIII antibodies ,HEMOPHILIA ,BIOMARKERS - Abstract
Summary: We investigated longitudinally the behaviour of anti‐factor VIII (anti‐FVIII) IgG subclasses for 6 months from inhibitor development in 43 patients from the Survey of Inhibitors in Plasma‐Products Exposed Toddlers (SIPPET) trial who developed persistent or transient inhibitors. We first analysed 43 patients within 60 days post inhibitor detection. Then, 14 of these 43 patients were studied at five time points over 6 months. Our study showed that during the first 60 days, the risk of inhibitor persistence increased with the concomitant presence of an increasing number of IgG subclasses. Over the 6‐month period post inhibitor detection, only the IgG2 subclass could be considered a hallmark of inhibitor persistence. [ABSTRACT FROM AUTHOR]
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- 2021
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12. Association of Risk of Incident and Recurrent Venous Thromboembolism with Oral Glucocorticoid Treatment
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Orsi, Fernanda Andrade, primary, Lijfering, Willem M, additional, Geersing, Geert-Jan, additional, Rosendaal, Frits Richard, additional, Dekkers, Olaf, additional, le Cessie, Saskia, additional, and Cannegieter, Suzanne, additional
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- 2018
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13. Prediction of Anti-FVIII Inhibitor Persistence By Anti-FVIII IgG Subclasses in Patients with Severe Hemophilia — A in the Sippet Cohort Study
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Peyvandi, Flora, primary, Bucciarelli, Paolo, additional, Valsecchi, Carla, additional, Boscarino, Marco, additional, Palla, Roberta, additional, Santagostino, Elena, additional, El-Beshlawy, Amal, additional, Elalfy, Mohsen Saleh, additional, Ramanan, Vijay M., additional, Eshghi, Peyman, additional, Hanagavadi, Suresh, additional, Karimi, Mehran, additional, Ross, Cecil, additional, Manglani, Mamta V, additional, Young, Guy, additional, Seth, Tulika, additional, Apte, Shashikant, additional, Nayak, Dinesh M, additional, Mancuso, Maria Elisa, additional, Mahlangu, Johnny, additional, Santiago, Bonanad, additional, Cerqueira, Monica H, additional, Ewing, Nadia P, additional, Male, Christoph, additional, Owaidah, Tarek, additional, Soto Arellano, Veronica, additional, Majumdar, Suvankar, additional, Simpson, Mindy, additional, Thomas, Mathew, additional, Zanon, Ezio, additional, Manco-Johnson, Marilyn J, additional, Martinez, Monica, additional, Mazzucconi, Maria Gabriella, additional, Neme, Daniela, additional, Paredes-Aguilera, Rogelio Alejandro, additional, Prezotti, Alessandra N L, additional, Schmitt, Klaus, additional, Zulfikar, Bulent, additional, Mannucci, Pier Mannuccio, additional, and Rosendaal, Frits Richard, additional
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- 2018
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14. Existing data sources in clinical epidemiology: the Scandinavian Thrombosis and Cancer Cohort
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Jensvoll, Hilde, Severinsen, Marianne T., Hammerstrøm, Jens, Brækkan, Sigrid Kufaas, Kristensen, Søren R., Cannegieter, Suzanne C., Blix, Kristine, Tjønneland, Anne, Rosendaal, Frits Richard, Dziewiecka, Olga, Overvad, Kim, Næss, Inger Anne, and Hansen, John-Bjarne
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pulmonary embolism ,VDP::Medical disciplines: 700::Clinical medical disciplines: 750 ,venous thromboembolism ,VDP::Medisinske Fag: 700::Klinisk medisinske fag: 750 ,cancer ,Clinical Epidemiology ,incidence rates ,population-based cohort ,prospective ,person-years - Abstract
Hilde Jensvoll,1,2 Marianne T Severinsen,3,4 Jens Hammerstrøm,5 Sigrid K Brækkan,1,2 Søren R Kristensen,4,6 Suzanne C Cannegieter,7 Kristine Blix,1,2 Anne Tjønneland,8 Frits R Rosendaal,1,7,9 Olga Dziewiecka,1 Kim Overvad,10,11 Inger Anne Næss,12 John-Bjarne Hansen1,21Department of Clinical Medicine, KG Jebsen – Thrombosis Research and Expertise Center (TREC), UiT – The Arctic University of Norway, 2Division of Internal Medicine, University Hospital of North Norway, Tromsø, Norway; 3Department of Hematology, Aalborg University Hospital, 4Department of Clinical Medicine, Aalborg University, Aalborg, Denmark; 5Department of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway; 6Department of Clinical Biochemistry, Aalborg University Hospital, Aalborg, Denmark; 7Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, the Netherlands; 8Diet, Genes and Environment, Danish Cancer Society Research Center, Copenhagen, Denmark; 9Department of Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, the Netherlands; 10Department of Cardiology, Aalborg University Hospital, Aalborg, 11Department of Public Health, Section for Epidemiology, Aarhus University, Aarhus, Denmark; 12Department of Hematology, Trondheim University Hospital, Trondheim, NorwayBackground: Although venous thromboembolism (VTE) is a known common complication in cancer patients, there is limited knowledge on patient-related and cancer-specific risk factors in the general population. The Scandinavian Thrombosis and Cancer (STAC) Cohort was established by merging individual data from three large Scandinavian cohorts (The Tromsø Study, the second Nord-Trøndelag Health Study, and the Danish Diet, Cancer and Health Study). Here, we present the profile of the STAC cohort and provide age-specific incidence rates of VTE and cancerMethods: The STAC cohort includes 144,952 subjects aged 19–101 years without previous VTE or cancer. Baseline information collected in 1993–1997 included physical examination, self-administered questionnaires, and blood samples. Validated VTE events and cancer diagnoses were registered up to 2007–2012.Results: There were 2,444 VTE events (1.4 per 1,000 person-years [PY]) during follow-up, and the incidence increased exponentially from 0.3 per 1,000 PY in subjects aged 20–29 years to 6.4 per 1,000 PY in subjects aged 80+. Overall, 51% of the VTE events were provoked, and cancer was the most common provoking factor (19%), followed by immobilization and surgery (both 15%). In total, 19,757 subjects developed cancer during follow-up (9.8 per 1,000 PY), and the 5-year age-specific incidence rates of cancer were coherent with corresponding rates from the Norwegian Cancer Registry.Conclusion: The STAC cohort will provide a unique opportunity to explore the epidemiology and impact of genetic and environmental patient-related and cancer-specific risk factors for VTE in the general population.Keywords: venous thromboembolism, incidence rates, person-years, pulmonary embolism, population-based cohort, prospective, cancer
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- 2015
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15. Etiology, management, and outcome of the Budd-Chiari syndrome
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Murad, Sarwa Darwish, Janssen, Harry H.L.A., Plessier, Aurelie, Valla, Dominique, Hernandez-Guerra, Manuel, Garcia-Pagan, Juan-Carlos, Fabris, Federica, Primignani, Massimo, Eapen, Chundamannil Eapen, Elias, Elwyn, Bahr, Mathias M.J., Trebicka, Jonel, Heller, Jörg, Morard, Isabelle, Hadengue, Antoine, Lasser, Luc, Langlet, Philippe, Miranda, Helena, Leebeek, Frank F.W., Rosendaal, Frits Richard, Murad, Sarwa Darwish, Janssen, Harry H.L.A., Plessier, Aurelie, Valla, Dominique, Hernandez-Guerra, Manuel, Garcia-Pagan, Juan-Carlos, Fabris, Federica, Primignani, Massimo, Eapen, Chundamannil Eapen, Elias, Elwyn, Bahr, Mathias M.J., Trebicka, Jonel, Heller, Jörg, Morard, Isabelle, Hadengue, Antoine, Lasser, Luc, Langlet, Philippe, Miranda, Helena, Leebeek, Frank F.W., and Rosendaal, Frits Richard
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Background: The Budd-Chiari syndrome (BCS) is hepatic venous outflow obstruction. What is known about the syndrome is based on small studies of prevalent cases. Objective: To characterize the causes and treatment of incident BCS. Design: Consecutive case series of patients with incident BCS, enrolled from October 2003 to October 2005 and followed until May 2006. Setting: Academic and nonacademic hospitals in France, Spain, Italy, Great Britain, Germany, Belgium, the Netherlands, Portugal, and Switzerland. Patients: Persons older than 16 years with definite hepatic outflow obstruction diagnosed by imaging. Persons with hepatic outflow obstruction due to heart failure, sinusoidal obstruction syndrome, cancer, or liver transplantation were excluded. Measurements: Signs and symptoms; laboratory and imaging findings; diagnosis; treatment; and overall, transplantation-free, and intervention-free survival. Results: 163 incident cases of BCS were identified. Median follow-up was 17 months (range, 0.1 to 31 months). Most patients (84%) had at least 1 thrombotic risk factor, and many (46%) had more than 1; the most common was myeloproliferative disorders (49% of 103 tested patients). Patients were mainly treated with anticoagulation (140 patients [86%]), transjugular intrahepatic portosystemic shunting (56 patients [34%]), or liver transplantation (20 patients [12%]), and 80 patients (49%) were managed noninvasively. Only 3 patients underwent surgical shunting. The survival rate was 87% (95% CI, 82% to 93%) at 1 year and 82% (CI, 75% to 88%) at 2 years. Limitation: Treatment was not standardized across all centers, and data on important clinical variables were missing for some patients. Conclusion: Most patients with BCS have at least 1 thrombotic risk factor, and many have more than 1; myeloproliferative disorders are most common. One- and 2-year survival rates are good with contemporary management, which includes noninvasive therapies (anticoagulation and diuretics) and inv, SCOPUS: ar.j, info:eu-repo/semantics/published
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- 2009
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