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Baseline characteristics and evolution of Brazilian patients with atypical hemolytic uremic syndrome: first report of the Brazilian aHUS Registry.
Vaisbich MH, de Andrade LGM, de Menezes Neves PDM, Palma LMP, de Castro MCR, Silva CAB, de Holanda Barbosa MIN, Penido MGMG, Neto OÂF, Sobral RML, Miranda SMC, de Almeida Araújo S, Pietrobom IG, Takase HM, Ribeiro C, da Silva RM, de Carvalho CAA, Machado DJB, E Silva AMST, da Silva AR, Russo ER, Barros FHS, Nasserala JCL, de Oliveira LSC, de Castro Sylvestre L, Weissheimer R, Nascimento SO, Bianchini G, de Carvalho Barreto F, Veloso VSP, Fortes PM, Colares VS, Gomes JG, Leite AFP, Mesquita PGM, Vieira-Neto OM. Vaisbich MH, et al. Among authors: silva cab. Clin Kidney J. 2022 Apr 11;15(8):1601-1611. doi: 10.1093/ckj/sfac097. eCollection 2022 Aug. Clin Kidney J. 2022. PMID: 35892013 Free PMC article.
Renal Manifestations of Fabry Disease: A Narrative Review.
Silva CAB, Moura-Neto JA, Dos Reis MA, Vieira Neto OM, Barreto FC. Silva CAB, et al. Can J Kidney Health Dis. 2021 Jan 19;8:2054358120985627. doi: 10.1177/2054358120985627. eCollection 2021. Can J Kidney Health Dis. 2021. PMID: 33786192 Free PMC article. Review.
Assessment of combined α-GAL enzyme activity and lyso-GL3 for Fabry disease screening in women with chronic kidney disease.
Silva CAB, de Carvalho Barreto F, Neto OMV, Lucca LJ, Vieira FA, Gueiros APS, Boger MV, Silva AQ, Guedes FL, Israel KCP, Gordon GEM, Veloso VSP, Sevignani G, Barretto CT, Rosa MG, Pascotto RC, Ennes GS, da Silva Montenegro Malaguti Souza EM, Ribeiro MG, de Andrade LGM. Silva CAB, et al. Mol Genet Metab. 2024 Sep-Oct;143(1-2):108565. doi: 10.1016/j.ymgme.2024.108565. Epub 2024 Aug 16. Mol Genet Metab. 2024. PMID: 39182416 Free article.
Infrared spectroscopy as a new approach for early fabry disease screening: a pilot study.
Barretto CT, Nascimento MHC, Brun BF, da Silva TB, Dias PAC, Silva CAB, Singh MN, Martin FL, Filgueiras PR, Romão W, Campos LCG, Barauna VG. Barretto CT, et al. Among authors: silva cab. Orphanet J Rare Dis. 2024 Oct 10;19(1):373. doi: 10.1186/s13023-024-03380-x. Orphanet J Rare Dis. 2024. PMID: 39390597 Free PMC article.
67 results