CV Lattes
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Universidade Estadual de Campinas (UNICAMP). Faculdade de Ciências Médicas (FCM) (Institutional affiliation from the last research proposal) Birthplace: Brazil
Graduated as phisician in 1973 at Faculdade de Medicina de Ribeirão Preto - USP (1973), master's in Infectious Diseases at Medical Clinical Department from Faculdade de Medicina de Ribeirão Preto - USP (1978) and ph.d. in Infectious Diseases at Medical Clinical Department from Faculdade de Medicina de Ribeirão Preto - USP - Specialized in Infectious Diseases by the Brazilian Society of Infectious Diseases Specialized in Public Health by the Faculty of Medicine Ribeirão Preto University of São Paulo USP 1986 Pos-doctorate in Colindale UK with Tyrone Pitt 1991 . Professor Doctor level 2 of the Faculty of Medical Sciences - Department of Clinical Pathology since June 2005 Director of Division of Clinical Pathology at Hospital de Clinicas UNICAMP from May 2008 to May 2014,. Coordinator of the Bacteriology Lab, Mycobacteria Lab and Parasitology Lab. since june 2006 Acting on the following subjects: hospital infections, bacterial resistance, cystic fibrosis, virulence factors, opportunistic and emergent infecctions and environmental Microbiology. (Source: Lattes Curriculum)
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Cystic fibrosis (CF) is basically characterized by defective ion transport across the cell membrane in epithelial cells of the airways, pancreas, salivary glands, sweat, intestine and reproductive tract, resulting in mucosal secretions too thick and viscous, which cause obstruction at the level of glandular ducts and tubules. Certain systemic diseases, such as CF, may jeopardize the opera…
Cystic fibrosis (CF) is a genetic disease resulting from dysfunction of the CFTR protein, essential for the transport of ions and water across the cell membrane, and the lung disease is the most prominent clinical manifestation. Dehydration of the respiratory secretions occurs resulting in increased viscosity, impairing of mucociliary transport, developing chronic low airways obstruction,…
Introduction: cystic fibrosis (CF) is basically characterized by defective ion transport across the cell membrane in epithelial cells of the airways, pancreas, salivary glands, sweat, intestine and reproductive tract, resulting in mucosal secretions too thick and viscous, which cause obstruction at the level of glandular ducts and tubules. Certain systemic diseases, such as CF, may jeopar…
Cystic fibrosis (CF) is a genetic disease resulting from dysfunction of the CFTR protein, essential for the transport of ions and water across the cell membrane, and the lung disease is the most prominent clinical manifestation. Dehydration of the respiratory secretions occurs resulting in increased viscosity, impairing of mucociliary transport, developing chronic low airways obstruction,…
| 1 / 1 | Completed research grants |
| 2 / 2 | Completed scholarships in Brazil |
| 1 / 1 | Completed scholarships abroad |
| 4 / 4 | All research grants and scholarships |
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