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Universidade Federal de São Paulo (UNIFESP). Campus São Paulo. Escola Paulista de Medicina (EPM) (Institutional affiliation for the last research proposal) Birthplace: Brazil
Marcelle de Paula Ribeiro in research grants and scholarships supported by FAPESP.
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Pulmonary Arterial Hypertension (PAH) is a rare and progressive disease, with multiple etiologies and poor prognosis. The cardiovascular autonomic dysfunction plays a role on PAH pathophysiology, contributing to clinical deterioration and disease progression. Recently, clinical studies have been shown that the exacerbation of carotid chemoreflex activity might be one potential mechanism i…
Pulmonary Arterial Hypertension (PAH) is a chronic disease with varied etiology and unfavorable prognosis. The disease is accompanied by autonomic dysfunction, which is characterized by decreased parasympathetic activity and increased sympathetic activity to the cardiovascular system. One of the mechanisms that may contribute to the autonomic dysfunction in PAH is the increase in peripher…
Pulmonary Arterial Hypertension (PAH) is a rare and progressive disease with poor prognosis. In PAH, vascular impairment is not restricted to pulmonary circulation as systemic vascular dysfunction has been reported. Accumulating evidence from my PhD study and others have shown that an augmented carotid chemoreflex contributes to the sympathetic hyperactivity at rest and overall cardiovasc…
Pulmonary Arterial Hypertension (PAH) is a rare and progressive disease that affects the pulmonary vasculature. It is characterized by increase in resting pulmonary arterial pressure (PAP) and pulmonary vascular resistance (PVR) leading to right heart failure and death. Despite the pathophysiology of most forms of PAH remaining unclear, it is well established that autonomic nervous system…
| 2 / 2 | Completed scholarships in Brazil |
| 1 / 1 | Ongoing scholarships abroad |
| 1 / 1 | Completed scholarships abroad |
| 4 / 4 | All Scholarships |
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