Temis Maria Felix
Overview
Explore the profile of Temis Maria Felix including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
51
Citations
414
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Otavio A, Trescastro M, Silva H, Gomes E, Felix T
Codas
. 2025 Jan;
37(1):e20240052.
PMID: 39879426
Purpose: to characterize mastication and electrical activation of the masseter and anterior temporalis muscles in children and adolescents with osteogenesis imperfecta (OI), and relate results to guided occlusion and occlusal...
2.
de Oliveira B, Bernardi F, Baiochi J, Neiva M, Artifon M, Vergara A, et al.
Orphanet J Rare Dis
. 2024 Oct;
19(1):405.
PMID: 39478612
Background: The Brazilian Policy for Comprehensive Care for People with Rare Diseases was implemented in 2014; however, national epidemiological data on rare diseases (RDs) are scarce and mainly focused on...
3.
Felix T, de Oliveira B, Horovitz D
J Community Genet
. 2024 Sep;
PMID: 39325316
Rare diseases (RD) are individually rare, although encompass a significant proportion of the population, affecting not only the individuals but also their families. In Brazil RD is defined by the...
4.
Fernandes A, Felix T
Rev Paul Pediatr
. 2024 Sep;
43:e2023193.
PMID: 39258640
Objective: The aim of this study was to evaluate the functioning and associated factors in children and adolescents with osteogenesis imperfecta (OI). Methods: This is a cross-sectional study conducted on...
5.
Horovitz D, Felix T, de Faria Ferraz V
Genes (Basel)
. 2024 Aug;
15(8).
PMID: 39202336
Brazil is a continent-size country with 203 million inhabitants, classified as a developing upper-middle-income country, although inequities remain significant. Most of the population is assisted by the public Unified Health...
6.
de Queiroz Junior A, Vieira Sanseverino M, Collares M, Fornari A, do Virmond L, Filho J, et al.
Am J Med Genet A
. 2024 Aug;
194(12):e63836.
PMID: 39149840
Holoprosencephaly (HPE) results from a lack of cleavage of the prosencephalon. It has a complex etiology, resulting from chromosome abnormalities or single gene variants in the Sonic hedgehog signaling pathway....
7.
Silva I, Tacla M, Ribeiro E, Lustosa-Mendes E, Fett-Conte A, Felix T, et al.
J Pediatr (Rio J)
. 2024 Jul;
100(6):604-608.
PMID: 39053888
Objective: The current study delves into the accessibility of genetic evaluations for individuals with orofacial clefts (OC), comparing data between genetics and treatment centers across Brazil. Methods: This cross-sectional retrospective...
8.
Gomes M, Kehdy F, de Neves-Manta F, Horovitz D, Sanseverino M, Leal G, et al.
Sci Rep
. 2024 Jun;
14(1):13436.
PMID: 38862721
Cartilage-hair hypoplasia syndrome (CHH) is an autosomal recessive disorder frequently linked to n.72A>G (previously known as n.70A>G and n.71A>G), the most common RMRP variant worldwide. More than 130 pathogenic variants...
9.
de Wallau M, Xavier A, Moreno C, Kim C, Mendes E, Ribeiro E, et al.
Genes (Basel)
. 2024 Apr;
15(4).
PMID: 38674452
22q11.2 deletion syndrome (22q11.2DS) shows significant clinical heterogeneity. This study aimed to explore the association between clinical heterogeneity in 22q11.2DS and the parental origin of the deletion. The parental origin...
10.
Bernardi F, de Oliveira B, Yamada D, Artifon M, Schmidt A, Machado Scheibe V, et al.
J Med Internet Res
. 2023 Jul;
25:e44641.
PMID: 37498666
Background: The minimum data set (MDS) is a collection of data elements to be grouped using a standard approach to allow the use of data for clinical and research purposes....