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Molecular analyses of the vasopressin type 2 receptor and aquaporin-2 genes in Brazilian kindreds with nephrogenic diabetes insipidus.
Rocha JL, Friedman E, Boson W, Moreira A, Figueiredo B, Liberman B, de Lacerda L, Sandrini R, Graf H, Martins S, Puñales MK, De Marco L. Rocha JL, et al. Among authors: de lacerda l, de marco l. Hum Mutat. 1999;14(3):233-9. doi: 10.1002/(SICI)1098-1004(1999)14:3<233::AID-HUMU6>3.0.CO;2-O. Hum Mutat. 1999. PMID: 10477431
An Intron 9 CYP19 Gene Variant (IVS9+5G>A), Present in an Aromatase-Deficient Girl, Affects Normal Splicing and Is Also Present in Normal Human Steroidogenic Tissues.
Saraco N, Nesi-Franca S, Sainz R, Marino R, Marques-Pereira R, La Pastina J, Perez Garrido N, Sandrini R, Rivarola MA, de Lacerda L, Belgorosky A. Saraco N, et al. Among authors: de lacerda l. Horm Res Paediatr. 2015;84(4):275-82. doi: 10.1159/000437142. Epub 2015 Aug 5. Horm Res Paediatr. 2015. PMID: 26279340
Vocal Evaluation of Children with Congenital Hypothyroidism.
Dassie-Leite AP, Behlau M, Nesi-França S, Lima MN, de Lacerda L. Dassie-Leite AP, et al. Among authors: de lacerda l. J Voice. 2018 Nov;32(6):770.e11-770.e19. doi: 10.1016/j.jvoice.2017.08.006. Epub 2017 Oct 3. J Voice. 2018. PMID: 28986152
Pubertal development and adult height in patients with congenital hypothyroidism detected by neonatal screening in southern Brazil.
Nesi-França S, Silveira RB, Rojas Ramos JCR, Cardoso-Demartini AA, Lima Cat MN, de Carvalho JAR, Pereira RM, De Lacerda L. Nesi-França S, et al. Among authors: de lacerda l, de carvalho jar. J Pediatr Endocrinol Metab. 2020 Nov 26;33(11):1449-1455. doi: 10.1515/jpem-2020-0285. J Pediatr Endocrinol Metab. 2020. PMID: 33048835
78 results