Temis M Felix
Overview
Explore the profile of Temis M Felix including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
31
Citations
441
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0
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Recent Articles
1.
Spineli-Silva S, Monlleo I, Felix T, Gil-da-Silva-Lopes V, Vieira T
Cleft Palate Craniofac J
. 2023 May;
61(9):1578-1585.
PMID: 37183441
This study reports three patients with Cat-eye Syndrome (CES), two of which present a previous clinical diagnosis of Craniofacial microsomia (CFM). Chromosomal microarray analysis (CMA) revealed a tetrasomy of 1,7...
2.
McKnight D, Morales A, Hatchell K, Bristow S, Bonkowsky J, Perry M, et al.
JAMA Neurol
. 2022 Oct;
79(12):1267-1276.
PMID: 36315135
Importance: It is currently unknown how often and in which ways a genetic diagnosis given to a patient with epilepsy is associated with clinical management and outcomes. Objective: To evaluate...
3.
Spineli-Silva S, Sgardioli I, Dos Santos A, Bergamini L, Monlleo I, Fontes M, et al.
Am J Med Genet C Semin Med Genet
. 2020 Nov;
184(4):970-985.
PMID: 33215817
The aim of this study was to perform 22q11.2 deletion screening and chromosomal microarray analysis (CMA) in individuals clinically diagnosed with craniofacial microsomia (CFM) and review previously published cases of...
4.
Pinheiro B, Barrios P, Souza L, Felix T
Cardiol Young
. 2020 Aug;
30(10):1490-1495.
PMID: 32792038
Background: Osteogenesis imperfecta is a collagen type I bone disorder. Recently, extra-skeletal manifestations have been described, including many cardiovascular alterations. This study aims to report echocardiogram study in children with...
5.
Lustosa-Mendes E, Dos Santos A, Vieira T, Ribeiro E, Rezende A, Fett-Conte A, et al.
J Pediatr (Rio J)
. 2020 Jul;
97(3):321-328.
PMID: 32707036
Objective: This article presents a clinical and cytogenomic approach that focuses on the diagnosis of syndromic oral clefts (OCs). Methods: The inclusion criteria were individuals with OC presenting four or...
6.
Gomes M, Calatrava Paternostro L, Moura V, Antunes D, Caffarena E, Horovitz D, et al.
Mol Syndromol
. 2020 Feb;
10(5):255-263.
PMID: 32021596
Cartilage-hair hypoplasia syndrome (CHH) is an autosomal recessive disorder caused by pathogenic variants of the gene and characterized by metaphyseal bone dysplasia associated with hypotrichosis, immunodeficiency, and predisposition to malignancy....
7.
Magalhaes O, Rohenkohl H, Todeschini de Souza L, Schuler-Faccini L, Felix T
Cornea
. 2018 Oct;
37(12):1561-1565.
PMID: 30272615
Purpose: The goal of this study was to evaluate corneal profiles of patients with osteogenesis imperfecta (OI) due to a collagen I gene mutation. Methods: This was a cross-sectional comparative...
8.
Zambrano M, Felix T, de Mello E
Ann Nutr Metab
. 2017 Dec;
72(1):21-29.
PMID: 29268261
Background/aims: Osteogenesis Imperfecta (OI) is a bone disease characterized by bone fragility, deformities, and multiple fractures. The aim of this study was to compare the different methods of measuring the...
9.
Volpe-Aquino R, Monlleo I, Lustosa-Mendes E, Mora A, Fett-Conte A, Felix T, et al.
Birth Defects Res
. 2017 Sep;
110(1):72-80.
PMID: 28949457
Background: The World Health Organization has recognized the relevance of databases on craniofacial anomalies since . To date, there is no universal standard instrument/database focused on risk factors, clinical and...
10.
Correction: Biotinidase deficiency: Genotype-biochemical phenotype association in Brazilian patients
Borsatto T, Sperb-Ludwig F, Lima S, Carvalho M, Fonseca P, Camelo Jr J, et al.
PLoS One
. 2017 Jun;
12(6):e0180463.
PMID: 28640880
[This corrects the article DOI: 10.1371/journal.pone.0177503.].