CV Lattes
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Sociedade Beneficente Israelita Brasileira Albert Einstein (SBIBAE). Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE) (Institutional affiliation from the last research proposal) Birthplace: Brazil
bachelor's at Ciências Biológicas from Universidade Estadual Paulista Júlio de Mesquita Filho, UNESP, SJ Rio Preto (2006) and master's at Pathological Anatomy and Clinical Pathology from Faculdade de Medicina de São José do Rio Preto (2009). Has experience in Genetics, focusing on Human and Medical Genetics, acting on the following subjects: down syndrome, folic acid, síndrome de down, polymorphism and genetic polymorphisms. (Source: Lattes Curriculum)
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Down syndrome (DS), which is the consequence of the trisomy of chromosome 21 (T21), has an approximate incidence of 1:660 live births. DS is the most prevalent cause of intellectual disability of genetic origin and results in general cognitive impairment, which is typically in the mild-to-moderate range. Although DS has been known for over 160 years, our knowledge regarding the mechanisms…
Down syndrome (DS), also known as trisomy 21 (T21), which involves the presence of an extra copy of human chromosome 21 (HSA21), is the most common autosomal aneuploidy in live births. Intellectual disability is present in 100% of individuals, many of whom continue to experience learning and memory impairments and a higher risk of developing a neuropathology indistinguishable from Azheime…
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