Matheus Augusto Araujo Castro (Matheus Augusto Araújo Castro, Matheus A A Castro)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 16

Top Topics

Magnetic Resonance Imaging

Hypertrophic Cardiomyopathy

Intellectual Disability

Dna Methylation

Top Venues

American journal of medical genetics. Part A

Movement disorders clinical practice

Journal of human genetics

Arquivos de neuro-psiquiatria

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

Publications

Yuta Inoue, Naomi Tsuchida, Chong Ae Kim, Bruno de Oliveira Stephan, Matheus Augusto Araujo Castro, Rachel Sayuri Honjo, Debora Romeo Bertola, Yuri Uchiyama, Kohei Hamanaka, Atsushi Fujita, Eriko Koshimizu, Kazuharu Misawa, Satoko Miyatake, Takeshi Mizuguchi, Naomichi Matsumoto
Novel compound heterozygous ABCA2 variants cause IDPOGSA, a variable phenotypic syndrome with intellectual disability. Journal of human genetics (2024)
Thiago Gonçalves Guimarães, Jacy Bezerra Parmera, Matheus Augusto Araujo Castro, Rubens Gisbert Cury, Egberto Reis Barbosa, Fernando Kok
X-Linked Levodopa-Responsive Parkinsonism-Epilepsy Syndrome: A Novel PGK1 Mutation and Literature Review. Movement disorders clinical practice 11 (5) (2024)
Yuta Inoue, Naomi Tsuchida, Chong Ae Kim, Bruno de Oliveira Stephan, Matheus Augusto Araujo Castro, Rachel Sayuri Honjo, Debora Romeo Bertola, Yuri Uchiyama, Kohei Hamanaka, Atsushi Fujita, Eriko Koshimizu, Kazuharu Misawa, Satoko Miyatake, Takeshi Mizuguchi, Naomichi Matsumoto
Novel compound heterozygous ABCA2 variants cause IDPOGSA, a variable phenotypic syndrome with intellectual disability. Journal of human genetics 69 (3-4) (2024)
Thiago Gonçalves Guimarães, Jacy Bezerra Parmera, Matheus Augusto Araujo Castro, Rubens Gisbert Cury, Egberto Reis Barbosa, Fernando Kok
X-Linked Levodopa-Responsive Parkinsonism-Epilepsy Syndrome: A Novel PGK1 Mutation and Literature Review. Movement disorders clinical practice (2024)
Yuta Inoue, Naomi Tsuchida, Chong Ae Kim, Bruno de Oliveira Stephan, Matheus Augusto Araujo Castro, Rachel Sayuri Honjo, Debora Romeo Bertola, Yuri Uchiyama, Kohei Hamanaka, Atsushi Fujita, Eriko Koshimizu, Kazuharu Misawa, Satoko Miyatake, Takeshi Mizuguchi, Naomichi Matsumoto
Novel compound heterozygous ABCA2 variants cause IDPOGSA, a variable phenotypic syndrome with intellectual disability. Journal of human genetics 69 (3-4) (2024)
Thiago Gonçalves Guimarães, Jacy Bezerra Parmera, Matheus Augusto Araujo Castro, Rubens Gisbert Cury, Egberto Reis Barbosa, Fernando Kok
X-Linked Levodopa-Responsive Parkinsonism-Epilepsy Syndrome: A Novel PGK1 Mutation and Literature Review. Movement disorders clinical practice 11 (5) (2024)
Thiago Gonçalves Guimarães, Jacy Bezerra Parmera, Matheus Augusto Araujo Castro, Rubens Gisbert Cury, Egberto Reis Barbosa, Fernando Kok
X-Linked Levodopa-Responsive Parkinsonism-Epilepsy Syndrome: A Novel PGK1 Mutation and Literature Review. Movement disorders clinical practice 11 (5) (2024)
Ricardo Di Lazzaro Filho, Guilherme Lopes Yamamoto, Tiago J Silva, Leticia A Rocha, Bianca D W Linnenkamp, Matheus Augusto Araujo Castro, Deborah Bartholdi, André Schaller, Tosso Leeb, Samantha Kelmann, Claudia Y Utagawa, Carlos E Steiner, Leandra Steinmetz, Rachel Sayuri Honjo, Chong Ae Kim, Lisa Wang, Raphaël Abourjaili-Bilodeau, Philippe M Campeau, Matthew L Warman, Maria Rita Passos-Bueno, Nicolas C Hoch, Debora Romeo Bertola
Biallelic variants in DNA2 cause poikiloderma with congenital cataracts and severe growth failure reminiscent of Rothmund-Thomson syndrome. Journal of medical genetics (2023)
Paulo Ribeiro Nóbrega, Matheus Augusto Araujo Castro, Anderson Rodrigues Brandão de Paiva, Fernando Kok
Mystery solved after 23 years: M syndrome is PIGT-associated multiple congenital anomalies-hypotonia-seizures syndrome 3. American journal of medical genetics. Part A 188 (12) (2022)
Noriko Miyake, Chong Ae Kim, Kazuhiro Haginoya, Matheus Augusto Araujo Castro, Rachel Sayruri Honjo, Naomichi Matsumoto
De novo pathogenic DHX30 variants in two cases. Clinical genetics 100 (3) (2021)
Rachel Sayuri Honjo Kawahira, Matheus Augusto Araujo Castro, Suely Fazio Ferraciolli, Luiz Alberto Valente Soares Junior, Antonio Carlos Pastorino, Debora Romeo Bertola, Noriko Miyake, Naomichi Matsumoto, Chong Ae Kim
Cerebellofaciodental syndrome in an adult patient: Expanding the phenotypic and natural history characteristics. American journal of medical genetics. Part A 185 (5) (2021)
Matheus Augusto Araujo Castro, Juliana Heather Vedovato Dos Santos, Rachel Sayuri Honjo Kawahira, Guilherme Lopes Yamamoto, Debora Romeo Bertola, Anna C E Hurst, Lynn P Chorich, Lawrence C Layman, Chong Ae Kim, Hyung-Goo Kim
Twenty-year follow-up of the facial phenotype of Brazilian patients with Sotos syndrome. American journal of medical genetics. Part A 185 (12) (2021)
Toshiyuki Itai, Satoko Miyatake, Naomi Tsuchida, Ken Saida, Sho Narahara, Yu Tsuyusaki, Matheus Augusto Araujo Castro, Chong Ae Kim, Nobuhiko Okamoto, Yuri Uchiyama, Eriko Koshimizu, Kohei Hamanaka, Atsushi Fujita, Takeshi Mizuguchi, Naomichi Matsumoto
Novel CLTC variants cause new brain and kidney phenotypes. Journal of human genetics (2021)
Yorran Hardman Araújo Montenegro, Carolina Fischinger Moura de Souza, Francyne Kubaski, Franciele Barbosa Trapp, Maira Graeff Burin, Kristiane Michelin-Tirelli, Sandra Leistner-Segal, Ana Carolina Brusius Facchin, Fernanda S Medeiros, Luciana Giugliani, Erlane Marques Ribeiro, Charles Marques Lourenço, Augusto César Cardoso Dos Santos, Márcia Gonçalves Ribeiro, Chong Ae Kim, Matheus Augusto Araujo Castro, Emília Katiane Embiruçu, Carlos Eduardo Steiner, Maria Lucia Castro Moreira, Hector Quintero Montano, Guilherme Baldo, Roberto Giugliani
Sanfilippo syndrome type B: Analysis of patients diagnosed by the MPS Brazil Network. American journal of medical genetics. Part A (2021)
Debora Romeo Bertola, Matheus Augusto Araujo Castro, Guilherme L Yamamoto, Rachel S Honjo, José Ricardo Ceroni, Michele M Buscarilli, Amanda B Freitas, Alexsandra C Malaquias, Alexandre C Pereira, Alexander A L Jorge, Maria Rita Passos-Bueno, Chong A Kim
Phenotype-genotype analysis of 242 individuals with RASopathies: 18-year experience of a tertiary center in Brazil. American journal of medical genetics. Part C, Seminars in medical genetics 184 (4) (2020)
Matheus Augusto Araujo Castro, Pedro Henrique Almeida Fraiman, Clecio de Oliveira Godeiro-Junior
Magnetic resonance imaging traits may help to differentiate Pelizaeus-Merzbacher and Pelizaeus-Merzbacher-like disease. Arquivos de neuro-psiquiatria 77 (8) (2019)