CV Lattes
ResearcherID
Universidade Federal de São Paulo (UNIFESP). Campus São Paulo. Escola Paulista de Medicina (EPM) (Institutional affiliation from the last research proposal) Birthplace: Brazil
graduation at biomedicina from Universidade Federal do Triângulo Mineiro (2011) and master's at Pathological Anatomy and Clinical Pathology from Faculdade de Medicina de São José do Rio Preto (2014). Has experience in Physiology, acting on the following subjects: meta-analysis, down syndrome, mthfr a1298c polymorphism, mthfr c667t polymorphism and folate metabolism. (Source: Lattes Curriculum)
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Down syndrome (DS) is the most common cause of intellectual disability of genetic etiology, affecting approximately 1 in 700 live births. Few advances have been made toward the elucidation of some of the mechanisms underlying the pathophysiology associated with DS, including the role of the gamma-aminobutyric acid (GABA), the major inhibitory neurotransmitter in the mature central nervous…
Down Syndrome is the most common cause mental deficiency of genetic etiology, present in approximately one case per 600-700 births, making it the most common condition of aneuploidy compatible with life. In 95% of cases, is attributed to free trisomy of chromosome 21 resulting from maternal meiotic nondisjunction.It is well established that advanced maternal age is a risk factor for non-d…
Down syndrome (DS) is the most frequent cause of genetically defined intellectual disability, which results from the presence of an extra copy of chromosome 21. A wide range of neurological phenotypes is typically observed in persons with DS, including an increased incidence of seizure disorders. Mouse models of DS, particularly Ts65Dn mice, and emerging translational approaches, such as …
| 2 / 2 | Completed scholarships in Brazil |
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