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Epidemiological characterization of rare diseases in Brazil: A retrospective study of the Brazilian Rare Diseases Network.
Orphanet J Rare Dis. 2024 Oct 30;19(1):405. doi: 10.1186/s13023-024-03392-7.
Orphanet J Rare Dis. 2024.
PMID: 39478612
Free PMC article.
Clinical, radiographic, and genetic observations in 2 families with cleidocranial dysplasia.
Mestre VF, Spoladori IC, Osiak LB, Paiva WJM, Ferreira de Lima RL, Silveira BC, Salles MJS.
Mestre VF, et al. Among authors: paiva wjm.
Gen Dent. 2022 Jul-Aug;70(4):59-66.
Gen Dent. 2022.
PMID: 35749249
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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.
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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Partial monosomy of chromosome 21 and congenital malformations monosomy of chromosome 21 and malformations.
Osiak L, Saraiva JG, Mestre VF, Ferrari LSL, Paiva WJM, de Lima RLLF, Salles MJS.
Osiak L, et al. Among authors: paiva wjm.
Clin Dysmorphol. 2020 Jul;29(3):165-166. doi: 10.1097/MCD.0000000000000310.
Clin Dysmorphol. 2020.
PMID: 32501867
No abstract available.
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