- Research Grants
graduate at MEDICINA from Universidade Federal da Bahia (1997) and master's at Paediatrics from Universidade de São Paulo (2004). Has experience in Medicine (Source: Lattes Curriculum)
Noonan syndrome (NS) is an autosomal dominant disease characterized by postnatal short stature, facial dimorphisms, congenital heart disease and thoracic deformity. Germline mutations found in components of the RAS/MAPK signaling pathway have been described in patients with NS and other rare syndromes whose phenotype overlaps the SN, explaining the molecular cause in about 75 % of cases...
(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)
|Data from Web of Science|