CV Lattes
Universidade de São Paulo (USP). Faculdade de Medicina (FM) (Institutional affiliation from the last research proposal) Birthplace: Brazil
bachelor's at Medicina from Universidade de São Paulo (1971), master's at Neurology from Universidade de São Paulo (1982) and doctorate at Neurology from Universidade de São Paulo (1988). Has experience in Medicine, focusing on Medicine, acting on the following subjects: duchenne, corticoterapia, neurologia, tdah and crianças. (Source: Lattes Curriculum)
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The Congenital Muscular Dystrophies (CMD) are a clinically and genetically heterogeneous group of myopathies characterized by muscle hypotonia, delayed motor development and early onset of progressive muscle weakness with dystrophic pattern on muscle biopsy. Almost half of the cases is caused by deficiency of laminin-± 2 (merosin). Other protein deficiencies described include: collagen V…
The congenital muscular dystrophies (CMDs) are a group of genetically and clinically heterogeneous hereditary myopathies manifesting during the first year of life, that are characterized by congenital hypotonia, delayed motor development and early onset of progressive muscle weakness associated with dystrophic pattern on muscle biopsy. Many genes have been already identified, and almost 5…
(Only some records are available in English at this moment)
| 6 / 5 | Completed research grants |
| 2 / 0 | Completed scholarships in Brazil |
| 8 / 5 | All research grants and scholarships |
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