Marcela Costa

6PUBLICATIONS
50CO-AUTHORS
Optical technologyInfant and child healthGene and molecular therapyNeurology and neuromuscular diseasesAutonomic nervous system
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Publications (6)

|May 04, 2026
Ophthalmological Manifestations of Hereditary Amyloidosis due to Transthyretin: A Systematic Review.

|Mar 23, 2026
Unmet Needs in the Care of Patients with Duchenne Muscular Dystrophy in Brazil.

Alexandra Prufer de Queiroz Campos Araujo, Andre Vinícius Soares Barbosa, Michele Michelin Becker

|Apr 22, 2025
STAC3 gene congenital myopathy and malignant hyperthermia: a crossroads between neurology and anesthesia.

Mary Santos Silva, Ricardo Nakamura, Marcia Rosana Arjona

|Feb 05, 2024
Consensus from the Brazilian Academy of Neurology for the diagnosis, genetic counseling, and use of disease-modifying therapies in 5q spinal muscular atrophy.

Edmar Zanoteli, Alexandra Prufer de Queiróz Campos Araujo, Michele Michelin Becker

|Apr 14, 2023
Brazilian consensus for diagnosis, management and treatment of hereditary transthyretin amyloidosis with peripheral neuropathy: second edition.

Marcus Vinicius Pinto, Marcondes Cavalcante França, Marcus Vinicius Magno Gonçalves

|Oct 16, 2020
Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy.

Rodrigo de Holanda Mendonça, Ciro Matsui, Graziela Jorge Polido

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Frequent Collaborators

3 joint publications

Marcondes Cavalcante França Junior

2 joint publications

Alexandra Prufer de Queiroz Campos Araujo

2 joint publications

Michele Michelin Becker

2 joint publications

Wilson Marques