Overview
Marcos De Oliveira practices in Cuiaba, Brazil. Mr. De Oliveira is rated as an Experienced expert by MediFind in the treatment of Mitochondrial Complex 1 Deficiency. His top areas of expertise are Neuroblastoma, Embryonal Tumor with Multilayered Rosettes, Gliomatosis Cerebri, and Mitochondrial Complex 1 Deficiency.
His clinical research consists of co-authoring 68 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Mitochondrial Complex 1 Deficiency.
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Distinguished
- Embryonal Tumor with Multilayered RosettesMr. De Oliveira isDistinguished. Learn about Embryonal Tumor with Multilayered Rosettes.
- NeuroblastomaMr. De Oliveira isDistinguished. Learn about Neuroblastoma.
- Advanced
- Gliomatosis CerebriMr. De Oliveira isAdvanced. Learn about Gliomatosis Cerebri.
- Experienced
- Classic GalactosemiaMr. De Oliveira isExperienced. Learn about Classic Galactosemia.
- Galactokinase DeficiencyMr. De Oliveira isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMr. De Oliveira isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMr. De Oliveira isExperienced. Learn about Galactosemia.
- Mitochondrial Complex 1 DeficiencyMr. De Oliveira isExperienced. Learn about Mitochondrial Complex 1 Deficiency.