graduation at Farmácia Bioquímica from Universidade Estadual Paulista Júlio de Mesquita Filho (1997) and doctorate at Imunologia Básica e Aplicada from Faculdade de Medicina de Ribeirão Preto (2006). Has experience in Medicine, focusing on Hematology, acting on the following subjects: biorreator, terapia celular and bioprocesso. (Source: Lattes Curriculum)
| News published in Agência FAPESP Newsletter about the researcher |
| TITULO |
| Articles published in other media outlets (0 total): |
| More itemsLess items |
| VEICULO: TITULO (DATA) |
| VEICULO: TITULO (DATA) |
Sickle cell disorders (SCD) refers to a set of hemoglobinopathies (hereditary disorders of hemoglobin) caused by a point mutation at position 6 of the gene encoding the chain ²-globin, leading to physical-chemical changes in the hemoglobin molecule, yielding hemoglobin (Hb) abnormally S (HbS). The form of the disease where the two encoders of ²-globin alleles are mutated (i.e. are homozyg…
Defective apoptosis might be involved in the pathogenesis of multiple sclerosis (MS). We evaluated apoptosis-related molecules in MS patients before and after autologous hematopoietic stem cell transplantation (AHSCT) using BEAM or cyclophosphamide (CY) based conditioning regimens. Patients were followed for clinical and immunological parameters for two years after AHSCT. At baseline, MS …
Introduction: Type 1 diabetes mellitus (T1D) is characterized by autoimmune responses resulting in destruction of insulin-producing pancreatic beta cells. Multipotent mesenchymal stromal cells (MSCs) exhibit immunomodulatory potential, migratory capacity to injured areas and may contribute to tissue regeneration by the secretion of bioactive factors. Therefore, MSCs are considered as a pr…
(Only some records are available in English at this moment)
Systemic sclerosis (ES) is an autoimmune disease of the connective tissue, characterized by microvascular lesions, associated with different degrees of fibrosis of the skin and internal organs. ES is classified into two major clinical forms; ES limited and diffuse ES. These forms are differentiated by the extent of cutaneous involvement, by the serum profile of autoantibodies and by diffe…
Sickle cell anemia (SCA) is a monogenic disease characterized by chronic hemolytic anemia and vaso-occlusive phenomena that lead to acute painful crises and to tissue and organ, chronic and progressive damage. It is the most common monogenic hereditary disease of Brazil, occurring predominantly among African descendants, it is heterogeneously distributed being more frequent in the North a…
Sickle cell anemia (SCA) is the most common monogenic disease in the world , with important clinical, epidemiological and social impact. In Brazil, is the most common hereditary disease, occurring predominantly among Afrodescendants. The disease is characterized by chronic hemolytic anemia, chronic inflammatory and procoagulant state, and vaso-occlusive phenomena that lead to acute painfu…
(Only some records are available in English at this moment)
Autologous hematopoietic stem cell transplantation (AHSCT) has emerged as a novel therapy for systemic sclerosis (SSc) patients and induces long-term disease remission. In the last years, few works have reported the reconstitution of B-cell subsets after AHSCT. However, the assessment of B-cell receptor (BCR) diversity after AHSCT needs to be ascertained. Preliminary results of our group …
Sickle cell anemia (SCA) is a hereditary chronic condition disorder of hemoglobin (Hb) caused by a single missense mutation in the human ²-globin gene, resulting in the formation of an abnormal hemoglobin (HbS). The polymerization of the HbS under hypoxic conditions is a key event in the complex pathophysiology of SCA. In Brazil, it is related one new case of SCA in every 1000 births, sho…
| 8 / 7 | Completed research grants |
| 9 / 5 | Completed scholarships in Brazil |
| 2 / 2 | Completed scholarships abroad |
| 19 / 14 | All research grants and scholarships |
| Associated processes | |
CV Lattes
ORCID