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Year | Number of Results |
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2022 | 1 |
2023 | 5 |
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Page 1
Association between genetic factors and molar-incisor hypomineralisation or hypomineralised second primary molar: A systematic review.
Arch Oral Biol. 2023 Aug;152:105716. doi: 10.1016/j.archoralbio.2023.105716. Epub 2023 May 7.
Arch Oral Biol. 2023.
PMID: 37210809
Review.
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: mello de oliveira b.
J Med Internet Res. 2023 Jul 27;25:e44641. doi: 10.2196/44641.
J Med Internet Res. 2023.
PMID: 37498666
Free PMC article.
Review.
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A Broad Characterization of Glycogen Storage Disease IV Patients: A Clinical, Genetic, and Histopathological Study.
Wilke MVMB, de Oliveira BM, Starosta RT, Shinawi M, Lu L, He M, Ma Y, Stoll J, de Souza CFM, de Siqueira ACM, Vieira SMG, Cerski CT, Refosco LF, Schwartz IVD.
Wilke MVMB, et al. Among authors: de oliveira bm.
Biomedicines. 2023 Jan 26;11(2):363. doi: 10.3390/biomedicines11020363.
Biomedicines. 2023.
PMID: 36830903
Free PMC article.
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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. Among authors: de oliveira bm.
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.
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Periodontal Ehlers-Danlos syndrome in early childhood: A case report of loss of deciduous teeth.
Martins RS, Muniz FWMG, Gondim JO, Maurique LS, Nolasco-Lopes CM, Oliveira BM, Carvalho RS.
Martins RS, et al. Among authors: oliveira bm.
J Indian Soc Periodontol. 2023 Jan-Feb;27(1):99-103. doi: 10.4103/jisp.jisp_266_22. Epub 2023 Jan 3.
J Indian Soc Periodontol. 2023.
PMID: 36873967
Free PMC article.
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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.
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.
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