Mara Lucia Schmitz Ferreira Santos

9PUBLICATIONS
119CO-AUTHORS
Respiratory diseasesRural clinical healthAutoimmunityInfant and child healthGene expression (incl. microarray and other genome-wide approaches)
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Publications (9)

|Sep 15, 2026
Rare diseases in Brazil: a nationwide analysis of the diagnostic odyssey.

|Jan 08, 2025
Characterization of patients treated at a rare disease referral service: a descriptive study, 2016-2021.

Everson Andrade de Carvalho, Roberto Del Claro Hopker, Gustavo Henrique Pedroso

|Aug 01, 2024
Brazilian consensus recommendations on the diagnosis and treatment of autoimmune encephalitis in the adult and pediatric populations.

Lívia Almeida Dutra, Pedro Victor de Castro Silva, João Henrique Fregadolli Ferreira

|Oct 04, 2023
Brazilian experts' consensus on the treatment of infantile epileptic spasm syndrome in infants.

Letícia Pereira de Brito Sampaio, Adélia Maria de Miranda Henriques-Souza, Mariana Ribeiro Marcondes da Silveira

|Jul 31, 2023
Predictive factors of genetic diagnosis and real-life impact of next-generation sequencing for children with epilepsy.

Gustavo Moura da Mata Machado Ferreira Pinto, Solena Ziemer Kusma Fidalski, Mara Lúcia Schmidt Ferreira Santos

|May 07, 2021
Genotype-phenotype studies in a large cohort of Brazilian patients with Hunter syndrome.

Juliana Alves Josahkian, Ana Carolina Brusius-Facchin, Alice Brinckmann Oliveira Netto

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Frequent Collaborators

5 joint publications

Daniel Almeida do Valle

3 joint publications

Raquel Tavares Boy da Silva

2 joint publications

Carolina Fischinger Moura de Souza

2 joint publications

Ida Vanessa Döederlein Schwartz