Marcos Paulo Miola

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 3

Top Topics

Intellectual Disability

Amyotrophic Lateral Sclerosis

Newly Diagnosed

Genetic Diversity

Top Venues

Ophthalmic genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Marcos Paulo Miola, Caroline Luise Prochaska, Guilherme Cardoso, Octávio Ricci Junior, Luiz Carlos de Mattos
A novel cisAB allele with a missense variant (c.971T>C) in the ABO gene of a Brazilian family. Vox sanguinis (2024)
Carine Prisco Arnoni, Nayara Morais Silva, Flavia Sant'Anna Silva, Rafael Martins Parreira, Tatiane Aparecida de Paula Vendrame, Marcos Paulo Miola, Janaína Muniz, Afonso Cortez, Marilia Valvasori, Evanilde Pereira de Araujo, Leandro Felipe Figueiredo Dalmazzo, Alyne Freitas, Flavia Latini, Lilian Castilho
Genetic diversity of Gerbich alleles in Brazilians reveals an unexpected prevalence of the GE:-2,-3,4 phenotype. Vox sanguinis (2023)
Alessandro Garcia Lopes, Gildásio Castello Almeida, Marcos Paulo Miola, Ronan Marques Teixeira, Francielly Camilla Bazilio Laurindo Pires, Rodolfo Andrade Miani, Luiz Carlos de Mattos, Cinara Cássia Brandão de Mattos, Lilian Castiglioni
Absence of significant genetic alterations in the VSX1, SOD1, TIMP3, and LOX genes in Brazilian patients with Keratoconus. Ophthalmic genetics (2021)