Têmis Maria Félix - Search Results

Year	Number of Results
2002	2
2003	2
2004	2
2005	1
2006	1
2010	1
2011	1
2012	4
2013	3
2014	6
2015	4
2016	3
2017	2
2018	1
2019	1
2020	4
2021	8
2022	5
2023	3
2024	1

1

22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity.

de Wallau MB, Xavier AC, Moreno CA, Kim CA, Mendes EL, Ribeiro EM, Oliveira A, Félix TM, Fett-Conte AC, Bonadia LC, Correia-Costa GR, Monlleó IL, Gil-da-Silva-Lopes VL, Vieira TP. de Wallau MB, et al. Among authors: felix tm. Genes (Basel). 2024 Apr 21;15(4):518. doi: 10.3390/genes15040518. Genes (Basel). 2024. PMID: 38674452 Free PMC article.

2

The Minimum Data Set for Rare Diseases: Systematic Review.

Bernardi FA, Mello de Oliveira B, Bettiol Yamada D, Artifon M, Schmidt AM, Machado Scheibe V, Alves D, Félix TM. Bernardi FA, et al. Among authors: felix tm. J Med Internet Res. 2023 Jul 27;25:e44641. doi: 10.2196/44641. J Med Internet Res. 2023. PMID: 37498666 Free PMC article. Review.

3

Availability of Genetic Tests in Public Health Services in Brazil: Data from the Brazilian Rare Diseases Network.

de Oliveira BM, Neiva MB, Carvalho I, Schwartz IVD, Alves D, Felix TM; Raras Network Group. de Oliveira BM, et al. Among authors: felix tm. Public Health Genomics. 2023;26(1):145-158. doi: 10.1159/000531547. Epub 2023 Jun 23. Public Health Genomics. 2023. PMID: 37356424 Free PMC article.

4

Challenges and recommendations to increasing the use of exome sequencing and whole genome sequencing for diagnosing rare diseases in Brazil: an expert perspective.

Félix TM, Fischinger Moura de Souza C, Oliveira JB, Rico-Restrepo M, Zanoteli E, Zatz M, Giugliani R. Félix TM, et al. Int J Equity Health. 2023 Jan 13;22(1):11. doi: 10.1186/s12939-022-01809-y. Int J Equity Health. 2023. PMID: 36639662 Free PMC article. Review.

5

Increased Serum Levels of miR-125b and miR-132 in Fragile X Syndrome: A Preliminary Study.

Couto RR, Kubaski F, Siebert M, Félix TM, Brusius-Facchin AC, Leistner-Segal S. Couto RR, et al. Among authors: felix tm. Neurol Genet. 2022 Oct 26;8(6):e200024. doi: 10.1212/NXG.0000000000200024. eCollection 2022 Dec. Neurol Genet. 2022. PMID: 36313066 Free PMC article.

6

Achondroplasia in Latin America: practical recommendations for the multidisciplinary care of pediatric patients.

Llerena J Jr, Kim CA, Fano V, Rosselli P, Collett-Solberg PF, de Medeiros PFV, Del Pino M, Bertola D, Lourenço CM, Cavalcanti DP, Félix TM, Rosa-Bellas A, Rossi NT, Cortes F, Abreu F, Cavalcanti N, Ruz MCH, Baratela W. Llerena J Jr, et al. Among authors: felix tm. BMC Pediatr. 2022 Aug 19;22(1):492. doi: 10.1186/s12887-022-03505-w. BMC Pediatr. 2022. PMID: 35986266 Free PMC article.

7

Epidemiology of rare diseases in Brazil: protocol of the Brazilian Rare Diseases Network (RARAS-BRDN).

Félix TM, de Oliveira BM, Artifon M, Carvalho I, Bernardi FA, Schwartz IVD, Saute JA, Ferraz VEF, Acosta AX, Sorte NB, Alves D; RARAS Network group. Félix TM, et al. Orphanet J Rare Dis. 2022 Feb 24;17(1):84. doi: 10.1186/s13023-022-02254-4. Orphanet J Rare Dis. 2022. PMID: 35209917 Free PMC article.

8

Tympanic Membrane Retractions in patients with Williams Syndrome: A Controlled Study.

Oliveira MW, Lavinsky J, Valerio MM, Felix TM, Lavinsky L. Oliveira MW, et al. Among authors: felix tm. Int Arch Otorhinolaryngol. 2021 Jul;25(3):e443-e445. doi: 10.1055/s-0040-1715151. Epub 2020 Oct 15. Int Arch Otorhinolaryngol. 2021. PMID: 34377182 Free PMC article.

9

Does universal newborn hearing screening impact the timing of deafness treatment?

Faistauer M, Silva AL, Dominguez DOR, Bohn R, Félix TM, Costa SSD, Rosito LPS. Faistauer M, et al. Among authors: felix tm. J Pediatr (Rio J). 2022 Mar-Apr;98(2):147-154. doi: 10.1016/j.jped.2021.04.008. Epub 2021 Jun 21. J Pediatr (Rio J). 2022. PMID: 34166624 Free PMC article.

10

Craniofacial microsomia: Reflections on diagnosis and severity assessment based on a series of cases.

Bergamini LL, Spineli-Silva S, Félix TM, Gil-da-Silva-Lopes VL, Vieira TP, Ribeiro EM, Xavier AC, Lustosa-Mendes E, Fontes MÍB, Monlleó IL. Bergamini LL, et al. Among authors: felix tm. Congenit Anom (Kyoto). 2021 Sep;61(5):148-158. doi: 10.1111/cga.12422. Epub 2021 May 10. Congenit Anom (Kyoto). 2021. PMID: 33900643

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