Mafort Mafort

Dr. Mafort Mafort

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Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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23 December 2013 in Diabetology & Metabolic Syndrome
Verified
Journal Article
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EGErika P Guedes
Erika P Guedes
EMEduardo Madeira
Eduardo Madeira
MMMafort Mafort
Mafort Mafort
MMMiguel Madeira
Miguel Madeira
RMRodrigo O Moreira
Rodrigo O Moreira
MFMaria Lúcia Fleiuss De Farias
Maria Lúcia Fleiuss De Farias
Several studies point to a correlation between obesity and the severity of depressive and anxiety symptoms in children and adults, but there are still some controversial points about this association. The aim of this study is to investigate the relationship between body composition and the severity of anxiety/depressive symptoms in overweight and obese individuals with Metabolic Syndrome (MS).

1 February 2014 in Bone
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Journal Article
Closed access
EMEduardo Madeira
Eduardo Madeira
MMMafort Mafort
Mafort Mafort
MMMiguel Madeira
Miguel Madeira
EGErika Paniago Guedes
Erika Paniago Guedes
RMRodrigo Oliveira Moreira
Rodrigo Oliveira Moreira
MFMaria Lúcia Fleiuss De Farias
Maria Lúcia Fleiuss De Farias

30 September 2020 in Journal of Ultrasound in Medicine
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Journal Article
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Agnaldo José LopesAgnaldo José Lopes
Agnaldo José Lopes
MMMafort Mafort
Mafort Mafort
CCClaudia HENRIQUE Costa
Claudia HENRIQUE Costa
RRRogério Rufino
Rogério Rufino
MFMônica de Cássia Firmida
Mônica de Cássia Firmida
RMRoberto Mogami
Roberto Mogami

16 August 2013 in Obesity Surgery
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Journal Article
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MMMafort Mafort
Mafort Mafort
EMEduardo Madeira
Eduardo Madeira
MMMiguel Madeira
Miguel Madeira
EGErika Paniago Guedes
Erika Paniago Guedes
RMRodrigo Oliveira Moreira
Rodrigo Oliveira Moreira
Agnaldo José LopesAgnaldo José Lopes
Agnaldo José Lopes

17 October 2019 in BMC Immunology
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Journal Article
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RSRenan Jeremias da Silva
Renan Jeremias da Silva
RCRaquel da Silva Corrêa
Raquel da Silva Corrêa
ISIsabela Gama Sardella
Isabela Gama Sardella
AMAna Carla de Paulo Mulinari
Ana Carla de Paulo Mulinari
MMMafort Mafort
Mafort Mafort
MSMaria Helena Feres Saad
Maria Helena Feres Saad
Background: A previous study demonstrated pleural fluid (PF) IgA immunodominance for the fused MT10.3:MPT64 protein in pleural tuberculosis (PLTB) cases. However, no clue on the role of IgA and IgG against this and other antigens in PF and serum concerning improved diagnosis is available. Thus, the aim of the present study was to validate PF IgA-MT10.3:MPT64 and evaluate PF and serum IgA and IgG reactivity against this protein, its peptides (F2) and single MPT64, MT10.3 and the PPE59 mycobacterial specific antigens. IgA and IgG ELISA were measured against the antigen in PLTB (n = 29) and other non-TB pleurisy (n = 39) patient samples. Results: The immunodominance of PF IgA-MT10.3:MPT64 was confirmed in PLTB (86.2%) followed by PPE59 (62%), while serum IgA-F2 exhibited 51.7% sensitivity. PF and serum IgG-MT10.3:MPT64 led to 65.5 and 51.7% sensitivity, respectively. However, MT10.3 and MPT64 displayed overall lower sensitivity (≤34.5) for both antibodies. All results at 95% fixed specificity. Combinatory results indicated 93.1% sensitivity for PF IgA-MT10.3:MPT64/−PPE59 and IgA/IgG-MT10.3:MPT64 at 92.3% specificity, followed by IgA-MT10.3:MPT64/−MPT64 or /−F2 (89.6%) without jeopardizing specificity (94.9%). The combinatory results of the PF adenosine deaminase test (ADA) and IgA-MT10.3:MPT64/−F2 demonstrated the highest sensitivity (96.6%), with a specificity of 92.3%. Conclusions: The PF IgA-MT10:MPT64 immune dominance was validated in PLTB, and its combinatory results with PPE59 or MPT64 or F2 antigens as well as with IgG, are reported herein for the first time, improving their potential to assist diagnosis. Combining PF-ADA and IgA-MT10.3:MPT64/−F2 results achieved better accuracy. Moreover, serum IgG, although less accurate, displays potential beyond microbiological tests.

9 April 2021 in The Ultrasound Journal
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Journal Article
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MMMafort Mafort
Mafort Mafort
RRRogerio Rufino
Rogerio Rufino
CCClaudia HENRIQUE Costa
Claudia HENRIQUE Costa
MCMariana Soares da Cal
Mariana Soares da Cal
LMLaura Braga Monnerat
Laura Braga Monnerat
Agnaldo José LopesAgnaldo José Lopes
Agnaldo José Lopes
Background: The role of lung ultrasound (LUS) in evaluating the mid- and long-term prognoses of patients with COVID-19 pneumonia is not yet known. The objectives of this study were to evaluate associations between LUS signs at the time of screening and clinical outcomes 1 month after LUS and to assess LUS signs at the time of presentation with known risk factors for COVID-19 pneumonia. Methods: This was a retrospective study of data prospectively collected 1 month after LUS screening of 447 adult patients diagnosed with COVID-19 pneumonia. Sonographic examination was performed in screening tents with the participants seated. The LUS signs (B-lines > 2, coalescent B-lines, and subpleural consolidations) were captured in six areas of each hemithorax and a LUS aeration score was calculated; in addition, the categories of disease probability based on patterns of LUS findings (high-probability, intermediate-probability, alternate, and low-probability patterns) were evaluated. The LUS signs at patients’ initial evaluation were related to the following outcomes: symptomatology, the need for hospitalization or invasive mechanical ventilation (IMV), and COVID-19-related death. Results: According to the evaluations performed 1 month after LUS screening, 36 patients were hospitalised, eight of whom required intensive care unit (ICU) admission and three of whom died. The presence of coalescent B-lines was associated with the need for hospitalization ( p = 0.008). The presence of subpleural consolidations was associated with dyspnoea ( p < 0.0001), cough ( p = 0.003), the need for hospitalization ( p < 0.0001), the need for ICU admission ( p < 0.0001), and death ( p = 0.002). A higher aeration score was associated with dyspnoea ( p < 0.0001), the need for hospitalization ( p < 0.0001), the need for ICU admission ( p < 0.0001), and death ( p = 0.003). In addition, patients with a high-probability LUS pattern had a higher aeration score ( p < 0.0001) and more dyspnoea ( p = 0.024) and more often required hospitalization ( p < 0.0001) and ICU admission ( p = 0.031). Conclusions: In patients with COVID-19 pneumonia, LUS signs were related to respiratory symptoms 1 month after LUS screening. Strong relationships were identified between LUS signs and the need for hospitalization and death.