Integrated Master in Medicine (Academic Degree Recognition)
Alameda Prof. Hernâni Monteiro, 4200-319, Porto. sigarra.up.pt
Clinical Physician • Medical Genetics Specialist • Master in Medicine and Infectious Parasitic Diseases
Born: 08/14/1983 • Nationality: Brazilian/Italian • CRM 52904848 • Medical Council 75438
Alameda Prof. Hernâni Monteiro, 4200-319, Porto. sigarra.up.pt
Av. Rui Barbosa, 716, Flamengo, 22250-020, Rio de Janeiro, Brazil. iff.fiocruz.br
Av. Brasil, 4365, Manguinhos, 21040-900, Rio de Janeiro, Brazil. fiocruz.br/ioc
Av. Barão do Rio Branco, 1003, Centro, 25680-120, Petrópolis, Brazil. fmpfase.edu.br
Medicine of the Future: Quantum Precision Medicine in Clinical Practice (2025)
Oliveira GM. 1st ed. 2 vols (1386 pp.). Available at: Amazon Kindle.
Website: Medicine of the Future.
High prevalence of hepatitis A in indigenous population in north Brazil (2020)
de Paula VS et al. BMC Res Notes. 2020 Sep 29;13(1):458. PMC7526101.
Clinical and neuropsychological assessment of attention and ADHD comorbidity in a sample of children and adolescents with idiopathic epilepsy (2015)
Costa CR et al. Arq Neuropsiquiatr. 2015 Feb;73(2):96–103. scielo.br.
Novel pathogenic mutation characterized in a patient with X-linked severe combined immunodeficiency (XSCID) (2015)
Oliveira GMO et al. Proceedings of the XXVII Brazilian Congress of Medical Genetics, Ribeirão Preto.
Epidemiological profile of patients with primary health care deficiencies and rare disease policy (2015)
Vieira DKR et al. Proceedings of the XXVII Brazilian Congress of Medical Genetics, Ribeirão Preto.
Most common congenital malformations recorded in the three largest reference health units of Mozambique’s national health system from 2010 to 2013 (2015)
Madeira LFA et al. Proceedings of the XXVII Brazilian Congress of Medical Genetics, Ribeirão Preto.
Analysis of renal malformations observed in neonatal autopsies at the National Institute of Women’s, Children’s and Adolescent Health Fernandes Figueira (2015)
Ramos LLP et al. Proceedings of the XXVII Brazilian Congress of Medical Genetics, Ribeirão Preto.
Case report of a family with type V osteogenesis imperfecta with molecular confirmation (2015)
Couto RGT et al. Proceedings of the XXVII Brazilian Congress of Medical Genetics, Ribeirão Preto.
Transient myeloproliferative disease in a newborn with non-immune hydrops and Down syndrome (2015)
Ramos LLP et al. Revista de Pediatria SOPERJ. 2015;15(suppl 1)(2):19.
Primary immunodeficiency, a translational and personalized genetics approach (2014)
Oliveira GMO et al. Poster at the XXVI Brazilian Congress of Medical Genetics, Fortaleza/CE; Special Supplement, Rev. Bras. Promoção Saúde. 2014;5(103).
Tay-Sachs disease variant B1 (2014)
Freitas MR et al. In: XI Congress of Pediatrics of the State of RJ (CONSOPERJ), Rio de Janeiro.
Pompe disease: a treatable metabolic disorder with different presentations (2014)
Correia PS et al. In: XI Congress of Pediatrics of the State of RJ (CONSOPERJ), Rio de Janeiro.
Identification of osteogenesis imperfecta by obstetric ultrasound and its importance in delivery (2014)
Germer R et al. In: XI Congress of Pediatrics of the State of RJ (CONSOPERJ), Rio de Janeiro.
Pattern of congenital defects in neonates at a tertiary maternity member of ECLAMC (2013)
Lucidi AR et al. In: XXV Brazilian Congress of Medical Genetics, Florianópolis.
Demyelinating disease presenting as Devic’s neuromyelitis optica (2008)
Oliveira GMO et al. In: XXIII Brazilian Congress of Neurology, Belém/PA.