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Alterations in microRNA of extracellular vesicles associated with major depression, attention-deficit/hyperactivity and anxiety disorders in adolescents.
Honorato-Mauer J, Xavier G, Ota VK, Chehimi SN, Mafra F, Cuóco C, Ito LT, Ormond R, Asprino PF, Oliveira A, Bugiga AVG, Torrecilhas AC, Bressan R, Manfro GG, Miguel EC, Rohde LA, Pan PM, Salum GA, Pellegrino R, Belangero S, Santoro ML. Honorato-Mauer J, et al. Among authors: chehimi sn. Transl Psychiatry. 2023 Feb 6;13(1):47. doi: 10.1038/s41398-023-02326-4. Transl Psychiatry. 2023. PMID: 36746925 Free PMC article.
Expanding the Phenotype of 8p23.1 Deletion Syndrome: Eight New Cases Resembling the Clinical Spectrum of 22q11.2 Microdeletion.
Montenegro MM, Camilotti D, Quaio CRDC, Gasparini Y, Zanardo ÉA, Rangel-Santos A, Novo-Filho GM, Francisco G, Liro L, Nascimento A, Chehimi SN, Soares DCQ, Krepischi ACV, Grassi MS, Honjo RS, Palmeira P, Kim CA, Carneiro-Sampaio MMS, Rosenberg C, Kulikowski LD. Montenegro MM, et al. Among authors: chehimi sn. J Pediatr. 2023 Jan;252:56-60.e2. doi: 10.1016/j.jpeds.2022.08.051. Epub 2022 Sep 5. J Pediatr. 2023. PMID: 36067875
Mosaic Trisomy 12 Associated with Overgrowth Detected in Fibroblast Cell Lines.
Gasparini Y, Montenegro MM, Novo-Filho GM, Ceroni JRM, Honjo RS, Zanardo ÉA, Dias AT, Nascimento AM, Costa TVMM, Madia FA, Chehimi SN, Damasceno JG, Kim CA, Kulikowski LD. Gasparini Y, et al. Among authors: chehimi sn. Cytogenet Genome Res. 2019;157(3):153-157. doi: 10.1159/000498836. Epub 2019 Apr 2. Cytogenet Genome Res. 2019. PMID: 30933946
Fetal gastroschisis: Maternal and fetal methylation profile.
Freitas AB, Francisco RPV, Centofanti SF, Damasceno JG, Chehimi SN, Osmundo-Junior GS, Kulikowski LD, Brizot ML. Freitas AB, et al. Among authors: chehimi sn. Prenat Diagn. 2021 Mar;41(4):449-456. doi: 10.1002/pd.5881. Epub 2021 Jan 3. Prenat Diagn. 2021. PMID: 33332636
Gene expression profile suggesting immunological dysregulation in two Brazilian Bloom's syndrome cases.
Montenegro MM, Quaio CR, Palmeira P, Gasparini Y, Rangel-Santos A, Damasceno J, Novak EM, Gimenez TM, Yamamoto GL, Ronjo RS, Novo-Filho GM, Chehimi SN, Zanardo EA, Dias AT, Nascimento AM, Costa TVMM, Duarte AJDS, Coutinho LL, Kim CA, Kulikowski LD. Montenegro MM, et al. Among authors: chehimi sn. Mol Genet Genomic Med. 2020 Apr;8(4):e1133. doi: 10.1002/mgg3.1133. Epub 2020 Feb 19. Mol Genet Genomic Med. 2020. PMID: 32073752 Free PMC article.
Cri-du-Chat Syndrome: Revealing a Familial Atypical Deletion in 5p.
Almeida VT, Chehimi SN, Gasparini Y, Nascimento AM, Carvalho GFS, Montenegro MM, Zanardo ÉA, Dias AT, Assunção NA, Kim CA, Kulikowski LD. Almeida VT, et al. Among authors: chehimi sn. Mol Syndromol. 2023 Jan;13(6):527-536. doi: 10.1159/000524371. Epub 2022 May 18. Mol Syndromol. 2023. PMID: 36660031 Free PMC article.
17 results