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Cardiovascular findings in classic homocystinuria.
Kalil MAB, Donis KC, Poswar FO, Dos Santos BB, Santos ÂBS, Schwartz IVD. Kalil MAB, et al. Among authors: donis kc. Mol Genet Metab Rep. 2020 Dec 10;25:100693. doi: 10.1016/j.ymgmr.2020.100693. eCollection 2020 Dec. Mol Genet Metab Rep. 2020. PMID: 33335839 Free PMC article.
Neurological outcomes after hematopoietic stem cell transplantation for cerebral X-linked adrenoleukodystrophy, late onset metachromatic leukodystrophy and Hurler syndrome.
Saute JA, Souza CF, Poswar FO, Donis KC, Campos LG, Deyl AV, Burin MG, Vargas CR, Matte UD, Giugliani R, Saraiva-Pereira ML, Vedolin LM, Gregianin LJ, Jardim LB. Saute JA, et al. Among authors: donis kc. Arq Neuropsiquiatr. 2016 Dec;74(12):953-966. doi: 10.1590/0004-282X20160155. Arq Neuropsiquiatr. 2016. PMID: 27991992 Free article.
Cytokines levels in late-diagnosed Classical Homocystinuria patients.
Poloni S, Siebert M, Donis KC, Weber Hoss GR, Blom HJ, Schwartz IVD. Poloni S, et al. Among authors: donis kc. Mol Genet Metab Rep. 2018 Sep 28;17:43-44. doi: 10.1016/j.ymgmr.2018.09.003. eCollection 2018 Dec. Mol Genet Metab Rep. 2018. PMID: 30294544 Free PMC article. No abstract available.
Ocular manifestations in classic homocystinuria.
Gus PI, Donis KC, Marinho D, Martins TF, de Souza CFM, Carloto RB, Leivas G, Schwartz IVD. Gus PI, et al. Among authors: donis kc. Ophthalmic Genet. 2021 Feb;42(1):71-74. doi: 10.1080/13816810.2020.1821384. Epub 2020 Sep 17. Ophthalmic Genet. 2021. PMID: 32940091
Clinical research challenges in rare genetic diseases in Brazil.
Giugliani L, Vanzella C, Zambrano MB, Donis KC, Wallau TKW, Costa FMD, Giugliani R. Giugliani L, et al. Among authors: donis kc. Genet Mol Biol. 2019;42(1 suppl 1):305-311. doi: 10.1590/1678-4685-GMB-2018-0174. Epub 2019 Jun 3. Genet Mol Biol. 2019. PMID: 31170279 Free PMC article.
39 results