Gustavo da Fontoura Galvão

Novel CCM1 (KRIT1) mutation detection in Brazilian familial Cerebral cavernous malformation: Different genetic variants in inflammation, oxidative stress and drug metabolism genes affect disease aggressiveness.

Ana Maria Blanco Martinez, S. Alves-Leon, S. A. Marques, 2020, World neurosurgery.

Elevated proportion of TLR2- and TLR4-expressing Th17-like cells and activated memory B cells was associated with clinical activity of cerebral cavernous malformations

J. M. de Souza, J. Hygino, C. Bento, 2022, Journal of neuroinflammation.

First Report of Concomitant Pathogenic Mutations Within MGC4607/CCM2 and KRIT1/CCM1 in a Familiar Cerebral Cavernous Malformation Patient.

Gustavo da Fontoura Galvão, Elielson Veloso da Silva, J. Marcondes de Souza, 2020, World neurosurgery.

Comprehensive CCM3 Mutational Analysis in Two Patients with Syndromic Cerebral Cavernous Malformation

J. M. de Souza, J. M. Souza, F. L. Fontes-Dantas, 2023, Translational stroke research.

Association of Variants in FCGR2A, PTPN2 and GM-CSF with Cerebral Cavernous Malformation: Potential Biomarkers for Symptomatic Disease.

F. L. Fontes-Dantas, Gustavo da Fontoura Galvão, S. Alves‐Leon, 2021, Current Neurovascular Research.