CV Lattes
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Universidade de São Paulo (USP). Faculdade de Medicina (FM) (Institutional affiliation from the last research proposal) Birthplace: Brazil
graduation at Ciências Biológicas - Modalidade Médica from Universidade Federal de São Paulo (1994), graduation at Medicina from Faculdade de Medicina da Universidade de São Paulo (2001), master's at Ciências Biológicas - Modalidade Médica from Universidade Federal de São Paulo (1997) and doctorate at Ciências Biológicas - Modalidade Médica from Universidade Federal de São Paulo (2001). He is currently bolsista de produtividade de cnpq at Conselho Nacional de Desenvolvimento Científico e Tecnológico and bolsista de produtividade de cnpq at Conselho Nacional de Desenvolvimento Científico e Tecnológico. Has experience in Medicine, acting on the following subjects: dermatomiosite, miopatias inflamatorias idiopaticas, miopatias autoimunes sistêmicas, polimiosite and lupus eritematoso sistêmico. (Source: Lattes Curriculum)
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Systemic autoimmune myopathies (SAMs) - including dermatomyositis (DM), polymyositis (PM), immune-mediated necrotizing myopathy (IMNM), and anti-synthetase syndrome (ASyS) - are rare, chronic, and highly disabling diseases that primarily affect striated skeletal muscle. These conditions are associated with significant functional impairment, reduced quality of life, and increased morbidity…
Systemic autoimmune rheumatic diseases (SARDs) are comprised by a variety of diseases that may affect several organs and systems, including joints, muscles, and nerves. Despite drug treatment and guidance on performing regular physical exercises, the high frequency of fatigue, motor deficits, and chronic pain in these patients is remarkable. These factors, in turn, impair functional capac…
Systemic autoimmune myopathies (SAMs) are rare rheumatic diseases characterized clinically by progressive, symmetrical and predominantly proximal muscle limb weakness. SAMs may also affect joints, lung, heart and gastrointestinal tract. Despite drug treatment and guidance on performing regular physical exercises, the high frequency of fatigue and chronic pain in these patients is remarkab…
Idiopathic inflammatory myopathies (MII) are rare systemic autoimmune diseases associated with high morbidity and functional disability. They can be classified as dermatomyositis (DM), polymyositis (PM), immune-mediated necrotizing myopathy (IMNM), inclusion body myositis (IBM), among others. Patients have primarilt skeletal muscle involvement, accompanied by decreased muscle strength, mu…
(Only some records are available in English at this moment)
Idiopathic inflammatory myopathies (IIMs), also known as systemic autoimmune myopathies (SAMs), are a group of rare rheumatic diseases that predominantly affect striated skeletal muscle. However, other organs and systems - such as the skin, heart, lungs, and joints - can also be involved. Similar to other systemic autoimmune rheumatic diseases (SARDs), the detection of autoantibodies has …
Introduction. Takayasu arteritis (TAK) is a rare primary systemic vasculitis that predominantly affects the aorta and its branches. To date, there are limited studies that specifically evaluate the heterogeneous initial clinical manifestations and eventual initial alterations in vascular images, as well as the possible relationship between them; therefore, this restricted scenario motivat…
Systemic autoimmune rheumatic diseases are diseases that course with an inflammatory process, that is, fever, weight loss, swelling, diffuse/joint pain and fatigue, can affect organs and systems, and are generally characterized by a high prevalence of cardiovascular diseases and morbidity, in addition to presenting a reduction in functional capacity, leading to a reduction in the level of…
Granulomatosis with polyangiitis (GPA) is a primary systemic vasculitis associated with the anti-neutrophil cytoplasmic autoantibody (ANCA), characterized by the classic triad of involvement of the upper and lower airways, and kidneys. Similar to other systemic rheumatic diseases, patients with GPA have, among their systemic symptoms, fatigue. Moreover, some individuals, even after diseas…
Systemic Primary Vasculitis (SPV) refers to rare and heterogeneous diseases that present with blood vessel inflammation as their main feature. In addition, because of these diseases' chronic systemic manifestation, drug treatment, and/or comorbidities, patients with SPV have reductions in their quality of life, functional capability, aerobic capacity, and performance of activities of dail…
(Only some records are available in English at this moment)
| 1 / 1 | Ongoing grants |
| 8 / 8 | Completed research grants |
| 2 / 2 | Ongoing scholarships in Brazil |
| 21 / 19 | Completed scholarships in Brazil |
| 32 / 30 | All research grants and scholarships |
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