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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2009 2
2010 1
2011 4
2012 2
2013 5
2014 2
2015 5
2016 1
2017 1
2018 5
2019 12
2020 14
2021 12
2022 3
2023 11
2024 4

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75 results

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Page 1
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: schwartz ivd. Ophthalmic Genet. 2021 Feb;42(1):71-74. doi: 10.1080/13816810.2020.1821384. Epub 2020 Sep 17. Ophthalmic Genet. 2021. PMID: 32940091
Feeding difficulties in patients with Phenylketonuria.
Rocha ADFD, Martinez CC, Refosco LF, Tonon T, Schwartz IVD, Almeida ST. Rocha ADFD, et al. Among authors: schwartz ivd. Codas. 2023 Sep 25;35(6):e20210292. doi: 10.1590/2317-1782/20232021292pt. eCollection 2023. Codas. 2023. PMID: 37792814 Free PMC article.
Cardiovascular findings in classic homocystinuria.
Kalil MAB, Donis KC, Poswar FO, Dos Santos BB, Santos ÂBS, Schwartz IVD. Kalil MAB, et al. Among authors: schwartz ivd. 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.
Introduction to the special issue on Clinical Genetics in Latin America.
Prada CE, Cavalcanti D, Schwartz IVD, Zarate YA. Prada CE, et al. Among authors: schwartz ivd. Am J Med Genet C Semin Med Genet. 2020 Dec;184(4):873-875. doi: 10.1002/ajmg.c.31875. Epub 2020 Dec 22. Am J Med Genet C Semin Med Genet. 2020. PMID: 33354820 No abstract available.
The fructose-1,6-bisphosphatase deficiency and the p.(Lys204ArgfsTer72) variant.
Pinheiro FC, Ligabue-Braun R, Siqueira ACM, Matuella C, Souza CFM, Monteiro FP, Kok F, Schwartz IVD, Sperb-Ludwig F. Pinheiro FC, et al. Among authors: schwartz ivd. Genet Mol Biol. 2021 May 14;44(2):e20200281. doi: 10.1590/1678-4685-GMB-2020-0281. eCollection 2021. Genet Mol Biol. 2021. PMID: 33999094 Free PMC article.
GBA1 variants in Brazilian Gaucher disease patients.
Basgalupp SP, Altmann V, Vairo FPE, Schwartz IVD, Siebert M; MilitaoBrazilian Collaborative Group on Gaucher Disease. Basgalupp SP, et al. Among authors: schwartz ivd. Mol Genet Metab Rep. 2023 Sep 9;37:101006. doi: 10.1016/j.ymgmr.2023.101006. eCollection 2023 Dec. Mol Genet Metab Rep. 2023. PMID: 38053927 Free PMC article.
Follow-up of pre-motor symptoms of Parkinson's disease in adult patients with Gaucher disease type 1 and analysis of their lysosomal enzyme profiles in the CSF.
Wilke MVMB, Poswar F, Borelli WV, Michelin Tirelli K, Randon DN, Lopes FF, Pasetto FB, Sebastião FM, Iop GD, Faqueti L, da Silva LA, Kubaski F, Schuh AFS, Giugliani R, Schwartz IVD. Wilke MVMB, et al. Among authors: schwartz ivd. Orphanet J Rare Dis. 2023 Oct 2;18(1):309. doi: 10.1186/s13023-023-02875-3. Orphanet J Rare Dis. 2023. PMID: 37784132 Free PMC article.
75 results