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Page 1
Prenatal metal concentrations and physical abnormalities in the Japan Environment and Children's Study.
Nakamura Y, Kobayashi S, Cho K, Itoh S, Miyashita C, Yamaguchi T, Iwata H, Tamura N, Saijo Y, Ito Y, Seto Y, Honjo R, Ando A, Furuse Y, Manabe A, Kishi R; Japan Environment and Children’s Study (JECS) Group. Nakamura Y, et al. Among authors: honjo r. Pediatr Res. 2023 Oct 19. doi: 10.1038/s41390-023-02851-4. Online ahead of print. Pediatr Res. 2023. PMID: 37857850
Incidence of alveolar capillary dysplasia with misalignment of pulmonary veins in infants with unexplained severe pulmonary hypertension: The roles of clinical, pathological, and genetic testing.
Onda T, Akimoto T, Hayasaka I, Ikeda M, Furuse Y, Ando A, Nakamura Y, Honjo R, Manabe A, Furuta I, Cho K. Onda T, et al. Among authors: honjo r. Early Hum Dev. 2021 Apr;155:105323. doi: 10.1016/j.earlhumdev.2021.105323. Epub 2021 Jan 26. Early Hum Dev. 2021. PMID: 33578219
Correction: Prenatal metal concentrations and physical abnormalities in the Japan environment and children's study.
Nakamura Y, Kobayashi S, Cho K, Itoh S, Miyashita C, Yamaguchi T, Iwata H, Tamura N, Saijo Y, Ito Y, Seto Y, Honjo R, Ando A, Furuse Y, Manabe A, Kishi R; Japan Environment and Children’s Study (JECS) Group. Nakamura Y, et al. Among authors: honjo r. Pediatr Res. 2024 Mar 8. doi: 10.1038/s41390-024-03099-2. Online ahead of print. Pediatr Res. 2024. PMID: 38459222 No abstract available.
Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: A pilot study in Brazil.
Migliavacca MP, Sobreira J, Bermeo D, Gomes M, Alencar D, Sussuchi L, Souza CA, Silva JS, Kroll JE, Burger M, Guarischi-Sousa R, Villela D, Yamamoto GL, Milanezi F, Horigoshi N, Cesar RG, de Carvalho WB, Honjo RS, Bertola DR, Kim CA, de Souza L, Procianoy RS, Silveria RC, Rosenberg C, Giugliani R, Campana GA, Scapulatempo-Neto C, Sobreira N. Migliavacca MP, et al. Among authors: honjo rs. Am J Med Genet A. 2024 Jun;194(6):e63544. doi: 10.1002/ajmg.a.63544. Epub 2024 Jan 23. Am J Med Genet A. 2024. PMID: 38258498
Novel compound heterozygous ABCA2 variants cause IDPOGSA, a variable phenotypic syndrome with intellectual disability.
Inoue Y, Tsuchida N, Kim CA, de Oliveira Stephan B, Castro MAA, Honjo RS, Bertola DR, Uchiyama Y, Hamanaka K, Fujita A, Koshimizu E, Misawa K, Miyatake S, Mizuguchi T, Matsumoto N. Inoue Y, et al. Among authors: honjo rs. J Hum Genet. 2024 Apr;69(3-4):163-167. doi: 10.1038/s10038-024-01219-8. Epub 2024 Jan 17. J Hum Genet. 2024. PMID: 38228874
Brazilian growth charts for Williams-Beuren Syndrome at ages 2 to 18 years.
Strafacci ASL, Bertapelli F, Kim CA, Rivadeneira MJ, Honjo RS, Domenici Kulikowski L, Ferreira DM, Batista LC, Lopes VLGDS, Guerra Junior G. Strafacci ASL, et al. Among authors: honjo rs. J Pediatr (Rio J). 2024 May-Jun;100(3):277-282. doi: 10.1016/j.jped.2023.11.009. Epub 2024 Jan 2. J Pediatr (Rio J). 2024. PMID: 38182127 Free PMC article.
Clinical Characterization and Underlying Genetic Findings in Brazilian Patients with Syndromic Microcephaly Associated with Neurodevelopmental Disorders.
Tolezano GC, Bastos GC, da Costa SS, Scliar MO, de Souza CFM, Van Der Linden H Jr, Fernandes WLM, Otto PA, Vianna-Morgante AM, Haddad LA, Honjo RS, Yamamoto GL, Kim CA, Rosenberg C, Jorge AAL, Bertola DR, Krepischi ACV. Tolezano GC, et al. Among authors: honjo rs. Mol Neurobiol. 2024 Jan 5. doi: 10.1007/s12035-023-03894-8. Online ahead of print. Mol Neurobiol. 2024. PMID: 38180615
84 results