Temis Maria Felix
Overview
Explore the profile of Temis Maria Felix including associated specialties, affiliations and a list of published articles.
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51
Citations
414
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Recent Articles
11.
de Oliveira B, Neiva M, Carvalho I, Schwartz I, Alves D, Felix T
Public Health Genomics
. 2023 Jun;
26(1):145-158.
PMID: 37356424
Introduction: The Brazilian Policy for Comprehensive Care for People with Rare Diseases (BPCCPRD) was published in 2014, accrediting several reference centers and incorporating many genetic tests for the diagnosis of...
12.
Felix T, de Souza C, Oliveira J, Rico-Restrepo M, Zanoteli E, Zatz M, et al.
Int J Equity Health
. 2023 Jan;
22(1):11.
PMID: 36639662
Early diagnosis of genetic rare diseases is an unmet need in Brazil, where an estimated 10-13 million people live with these conditions. Increased use of chromosome microarray assays, exome sequencing,...
13.
Couto R, Kubaski F, Siebert M, Felix T, Brusius-Facchin A, Leistner-Segal S
Neurol Genet
. 2022 Oct;
8(6):e200024.
PMID: 36313066
Background And Objectives: Fragile X syndrome (FXS) is a neurodevelopmental disorder, identified as the most common cause of hereditary intellectual disability and monogenic cause of autism spectrum disorders (ASDs), caused...
14.
Llerena Jr J, Kim C, Fano V, Rosselli P, Collett-Solberg P, de Medeiros P, et al.
BMC Pediatr
. 2022 Aug;
22(1):492.
PMID: 35986266
Background: Achondroplasia is the most common bone dysplasia associated with disproportionate short stature, and other comorbidities, such as foramen magnum stenosis, thoracolumbar kyphosis, lumbar hyperlordosis, genu varum and spinal compression....
15.
Felix T, de Oliveira B, Artifon M, Carvalho I, Bernardi F, Schwartz I, et al.
Orphanet J Rare Dis
. 2022 Feb;
17(1):84.
PMID: 35209917
The Brazilian Policy of Comprehensive Care for People with Rare Diseases (BPCCPRD) was established by the Ministry of Health to reduce morbidity and mortality and improve the quality of life...
16.
Oliveira M, Lavinsky J, Valerio M, Felix T, Lavinsky L
Int Arch Otorhinolaryngol
. 2021 Aug;
25(3):e443-e445.
PMID: 34377182
The role of elastin in tympanic retractions and chronic otitis media is not well established. Williams Syndrome (WS), a pathology related to a mutation in the elastin gene, could generate...
17.
Faistauer M, Silva A, Dominguez D, Bohn R, Felix T, Costa S, et al.
J Pediatr (Rio J)
. 2021 Jun;
98(2):147-154.
PMID: 34166624
Objective: To evaluate the impact of the Universal Neonatal Hearing Screening (UNHS) on the age at diagnosis, beginning of treatment, and first cochlear implant surgery. Methods: A retrospective cohort study...
18.
Craniofacial microsomia: Reflections on diagnosis and severity assessment based on a series of cases
Bergamini L, Spineli-Silva S, Felix T, Gil-da-Silva-Lopes V, Vieira T, Ribeiro E, et al.
Congenit Anom (Kyoto)
. 2021 Apr;
61(5):148-158.
PMID: 33900643
This study aims to discuss diagnostic criteria and severity assessment for craniofacial microsomia (CFM). A series of 61 patients with diverse CFM phenotypes had their clinical data collected by experienced...
19.
Cardoso-Dos-Santos A, Medeiros-de-Souza A, Bremm J, Alves R, Araujo V, Leite J, et al.
Epidemiol Serv Saude
. 2021 Apr;
30(1):e2020835.
PMID: 33886939
Objective: To define the list of priority congenital anomalies for improving their recording on the Brazilian Live Birth Information System (Sinasc). Methods: Based on the International Statistical Classification of Diseases...
20.
Faistauer M, Silva A, Felix T, Todeschini de Souza L, Bohn R, Costa S, et al.
Braz J Otorhinolaryngol
. 2021 Apr;
88 Suppl 1:S33-S41.
PMID: 33839059
Introduction: Hearing loss etiology depends on the population studied as well as on the ethnicity and the socio-economic condition of the analyzed region. Etiological diagnosis contributes to the improvement of...