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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.
Oral and maxillofacial manifestations of chronic kidney disease-mineral and bone disorder: a multicenter retrospective study.
Pontes FSC, Lopes MA, de Souza LL, Dos Santos da Mata Rezende D, Santos-Silva AR, Jorge J Jr, da Silva WG, Pires FR, Rocha AC, de Campos WG, Caldato MCF, Martin RM, Fonseca FP, Pontes HAR.
Pontes FSC, et al. Among authors: caldato mcf.
Oral Surg Oral Med Oral Pathol Oral Radiol. 2018 Jan;125(1):31-43. doi: 10.1016/j.oooo.2017.09.011. Epub 2017 Oct 10.
Oral Surg Oral Med Oral Pathol Oral Radiol. 2018.
PMID: 29104033
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High frequency of D727E polymorphisms in exon 10 of the TSHR gene in Brazilian patients with congenital hypothyroidism.
Alves EA, Cruz CM, Pimentel CP, Ribeiro RC, Santos AK, Caldato MC, Santana-da-silva LC.
Alves EA, et al.
J Pediatr Endocrinol Metab. 2010 Dec;23(12):1321-8. doi: 10.1515/jpem.2010.206.
J Pediatr Endocrinol Metab. 2010.
PMID: 21714466
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One-year clinical evaluation of single morning dose prednisolone therapy for 21-hydroxylase deficiency.
Caldato MC, Fernandes VT, Kater CE.
Caldato MC, et al.
Arq Bras Endocrinol Metabol. 2004 Oct;48(5):705-12. doi: 10.1590/s0004-27302004000500017. Epub 2005 Mar 7.
Arq Bras Endocrinol Metabol. 2004.
PMID: 15761542
Clinical Trial.
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