Matheus Augusto Araújo Castro

17PUBLICATIONS
79CO-AUTHORS
Neurology and neuromuscular diseasesNeonatologyMedical microbiology not elsewhere classifiedArtificial life and complex adaptive systemsGene expression (incl. microarray and other genome-wide approaches)
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Publications (17)

|Jul 07, 2026
Novel Homozygous Pathogenic Variant in DNAJC6 Causes Rapid Progressive Parkinsonism.

|Jun 15, 2026
Cognitive Decline, Neurologic Involvement, and Neonatal Crisis in ABCC9-Related Intellectual Disability and Myopathy Syndrome.

|Apr 29, 2026
A Novel TUBB2A Variant Causing Ataxia With Preserved Ambulation Into Adulthood.

|Nov 09, 2025
Correction: Novel compound heterozygous ABCA2 variants cause IDPOGSA, a variable phenotypic syndrome with intellectual disability.

Yuta Inoue, Naomi Tsuchida, Chong Ae Kim

|Jun 12, 2025
Clinical and Molecular Characterization of Xia-Gibbs Syndrome: Expanding the Phenotypic Spectrum in a Brazilian Cohort.

Maísa Ganz Sanchez Sennes, Laura Machado Lara Carvalho, Matheus Augusto Araújo Castro

|Dec 08, 2024
Split Hand-Foot Malformations-Unveiling Unique Molecular Diagnosis From a Brazilian Cohort.

Eduardo Da Cás, José Ricardo Magliocco Ceroni, Guilherme Lopes Yamamoto

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Frequent Collaborators

6 joint publications

Débora Romeo Bertola

6 joint publications

Chong Ae Kim

3 joint publications

Fernando Kok

3 joint publications

Naomichi Matsumoto