Félix TM - Search Results

1

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.

2

Mapping, Infrastructure, and Data Analysis for the Brazilian Network of Rare Diseases: Protocol for the RARASnet Observational Cohort Study.

Alves D, Yamada DB, Bernardi FA, Carvalho I, Filho MEC, Neiva MB, Lima VC, Félix TM. Alves D, et al. Among authors: felix tm. JMIR Res Protoc. 2021 Jan 22;10(1):e24826. doi: 10.2196/24826. JMIR Res Protoc. 2021. PMID: 33480849 Free PMC article.

3

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.

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

CranFlow: An Application for Record-Taking and Management Through the Brazilian Database on Craniofacial Anomalies.

Volpe-Aquino RM, Monlleó IL, Lustosa-Mendes E, Mora AF, Fett-Conte AC, Félix TM, Xavier AC, Tonocchi R, Ribeiro EM, Pereira R, Boy da Silva RT, de Rezende AA, Cavalcanti DP, Gil-da-Silva-Lopes VL. Volpe-Aquino RM, et al. Among authors: felix tm. Birth Defects Res. 2018 Jan 15;110(1):72-80. doi: 10.1002/bdr2.1123. Epub 2017 Sep 26. Birth Defects Res. 2018. PMID: 28949457

6

Molecular analysis of the CTSK gene in a cohort of 33 Brazilian families with pycnodysostosis from a cluster in a Brazilian Northeast region.

Araujo TF, Ribeiro EM, Arruda AP, Moreno CA, de Medeiros PF, Minillo RM, Melo DG, Kim CA, Doriqui MJ, Felix TM, Fock RA, Cavalcanti DP. Araujo TF, et al. Among authors: felix tm. Eur J Med Res. 2016 Aug 24;21(1):33. doi: 10.1186/s40001-016-0228-7. Eur J Med Res. 2016. PMID: 27558267 Free PMC article.

7

Calcium intake improvement after nutritional intervention in paediatric patients with osteogenesis imperfecta.

Zambrano MB, Félix TM, Mello ED. Zambrano MB, et al. Among authors: felix tm. J Hum Nutr Diet. 2019 Oct;32(5):619-624. doi: 10.1111/jhn.12657. Epub 2019 Apr 29. J Hum Nutr Diet. 2019. PMID: 31037781 Clinical Trial.

8

Difference between Methods for Estimation of Basal Metabolic Rate and Body Composition in Pediatric Patients with Osteogenesis Imperfecta.

Zambrano MB, Félix TM, de Mello ED. Zambrano MB, et al. Among authors: felix tm. Ann Nutr Metab. 2018;72(1):21-29. doi: 10.1159/000481918. Epub 2017 Dec 21. Ann Nutr Metab. 2018. PMID: 29268261

9

Vanz AP, van de Sande Lee J, Pinheiro B, Zambrano M, Brizola E, da Rocha NS, Schwartz IVD, de Souza Pires MM, Félix TM. Vanz AP, et al. Among authors: felix tm. BMC Pediatr. 2018 Mar 2;18(1):95. doi: 10.1186/s12887-018-1077-z. BMC Pediatr. 2018. PMID: 29499676 Free PMC article.

10

CLINICAL FEATURES AND PATTERN OF FRACTURES AT THE TIME OF DIAGNOSIS OF OSTEOGENESIS IMPERFECTA IN CHILDREN.

Brizola E, Zambrano MB, Pinheiro BS, Vanz AP, Félix TM. Brizola E, et al. Among authors: felix tm. Rev Paul Pediatr. 2017 Apr-Jun;35(2):171-177. doi: 10.1590/1984-0462/;2017;35;2;00001. Rev Paul Pediatr. 2017. PMID: 28977334 Free PMC article.

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