Cassiano Augusto Braga Silva
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Explore the profile of Cassiano Augusto Braga Silva including associated specialties, affiliations and a list of published articles.
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10
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50
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Recent Articles
1.
Barretto C, Nascimento M, Brun B, da Silva T, Dias P, Silva C, et al.
Orphanet J Rare Dis
. 2024 Oct;
19(1):373.
PMID: 39390597
Background: Fabry disease (FD) is a rare X-linked lysosomal storage disorder marked by alpha-galactosidase-A (α-Gal A) deficiency, caused by pathogenic mutations in the GLA gene, resulting in the accumulation of...
2.
Silva C, Barreto F, Neto O, Lucca L, Vieira F, Gueiros A, et al.
Mol Genet Metab
. 2024 Aug;
143(1-2):108565.
PMID: 39182416
Introduction: The spectrum of clinical presentation of Fabry disease (FD) in women is broad and challenging. The aim is to evaluate the effectiveness of an alternative screening method for FD...
3.
Vaisbich M, Modelli de Andrade L, de Menezes Neves P, Palma L, Castro M, Silva C, et al.
Clin Kidney J
. 2022 Jul;
15(8):1601-1611.
PMID: 35892013
Background: Atypical hemolytic uremic syndrome (aHUS) is an ultra-rare disease. Therefore, studies involving large samples are scarce, making registries powerful tools to evaluate cases. We present herein the first analysis...
4.
Vaisbich M, Modelli de Andrade L, Silva C, Barreto F
J Bras Nefrol
. 2022 Mar;
44(2):268-280.
PMID: 35238862
Fabry disease (FD) is a genetic disease, with X-chromosome linked inheritance, due to variants in the GLA gene that encodes the α-galactosidase A (α-GAL) enzyme. The purpose of the present...
5.
Silva C, Modelli de Andrade L, Vaisbich M, Barreto F
J Bras Nefrol
. 2022 Feb;
44(2):249-267.
PMID: 35212703
Fabry disease (FD) is an X-linked inherited disorder caused by mutations in the GLA gene encoding enzyme alpha-galactosidase A (α-Gal A). The purpose of this study was to produce a...
6.
Silva C, Moura-Neto J, Dos Reis M, Neto O, Barreto F
Can J Kidney Health Dis
. 2021 Mar;
8:2054358120985627.
PMID: 33786192
Purpose Of Review: In this narrative review, we describe general aspects, histological alterations, treatment, and implications of Fabry disease (FD) nephropathy. This information should be used to guide physicians and...
7.
Colares V, Miranda S, Modelli de Andrade L, Palma L, Castro M, Silva C, et al.
J Bras Nefrol
. 2020 Sep;
42(2 suppl 1):36-40.
PMID: 32877497
During the Covid-19 pandemic, the issue is how to maintain adequate care for people with other diseases. In this document, the SBN Rare Diseases Committee (COMDORA) gives some guidelines on...
8.
Moura-Neto J, Silva C, Moura A, Suassuna J
Kidney Int Rep
. 2019 May;
4(5):647-655.
PMID: 31080919
In recent years, Zika, Chikungunya, Dengue, West Nile Fever, and Yellow Fever epidemics have generated some concerns. Besides difficulties related to vector control, there are challenges related to behavior of...
9.
Biagini G, Almeida A, Almeida T, Silva C, Castro B, Reche T, et al.
J Bras Nefrol
. 2017 Oct;
39(3):333-336.
PMID: 29044343
Fabry disease is an X-linked lysosomal storage disease due to alpha-galactosidase A (α-Gal A) deficient activity which leads to the accumulation of glucoesphingolipids, such as globotriaosilceramide. There are over 700...
10.
Silva C, Barreto F, Dos Reis M, Junior J, Cruz C
Nephron
. 2016 Sep;
134(4):221-230.
PMID: 27576502
Introduction: Fabry disease (FD) is a lysosomal storage disorder caused by enzyme α galactosidase A (α-Gal A) deficiency due to mutations in the galactosidase alpha (GLA) gene. It leads to...