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Hepatocellular carcinoma in Gaucher disease: Reinforcing the proposed guidelines.
Starosta RT, Pinto E Vairo F, Dornelles AD, Cerski CTS, Álvares-da-Silva MR, Schwartz IVD. Starosta RT, et al. Among authors: schwartz ivd. Blood Cells Mol Dis. 2019 Feb;74:34-36. doi: 10.1016/j.bcmd.2018.10.004. Epub 2018 Oct 18. Blood Cells Mol Dis. 2019. PMID: 30446378 No abstract available.
Genetic analysis of patients with fructose-1,6-bisphosphatase deficiency.
Pinheiro FC, Sperb-Ludwig F, Ligabue-Braun R, Schüler-Faccini L, de Souza CFM, Vairo F, Schwartz IVD. Pinheiro FC, et al. Among authors: schwartz ivd. Gene. 2019 May 30;699:102-109. doi: 10.1016/j.gene.2019.03.007. Epub 2019 Mar 9. Gene. 2019. PMID: 30858132
Rare GBA1 genotype associated with severe bone disease in Gaucher disease type 1.
d'Avila Paskulin L, Starosta RT, Zizemer VS, Basgalupp S, Bertholdo D, Vairo FPE, Siebert M, Michelin-Tirelli K, Schwartz IVD. d'Avila Paskulin L, et al. Among authors: schwartz ivd. Mol Genet Metab Rep. 2019 Nov 22;21:100544. doi: 10.1016/j.ymgmr.2019.100544. eCollection 2019 Dec. Mol Genet Metab Rep. 2019. PMID: 31799121 Free PMC article.
Liver involvement in patients with Gaucher disease types I and III.
Starosta RT, Vairo FPE, Dornelles AD, Basgalupp SP, Siebert M, Pedroso MLA, Cerski CTS, Álvares-da-Silva MR, Schwartz IVD. Starosta RT, et al. Among authors: schwartz ivd. Mol Genet Metab Rep. 2020 Jan 7;22:100564. doi: 10.1016/j.ymgmr.2019.100564. eCollection 2020 Mar. Mol Genet Metab Rep. 2020. PMID: 32099816 Free PMC article.
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
215 results