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Page 1
Spontaneous puberty in girls with early diagnosis of Turner syndrome.
Carpini S, Carvalho AB, Guerra-Júnior G, Baptista MT, Lemos-Marini SH, Maciel-Guerra AT. Carpini S, et al. Arq Bras Endocrinol Metabol. 2012 Dec;56(9):653-7. doi: 10.1590/s0004-27302012000900009. Arq Bras Endocrinol Metabol. 2012. PMID: 23329189
408 Cases of Genital Ambiguity Followed by Single Multidisciplinary Team during 23 Years: Etiologic Diagnosis and Sex of Rearing.
De Paula GB, Barros BA, Carpini S, Tincani BJ, Mazzola TN, Sanches Guaragna M, Piveta CS, de Oliveira LC, Andrade JG, Guaragna-Filho G, Barbieri PP, Ferreira NM, Miranda ML, Gonçalves EM, Morcillo AM, Viguetti-Campos NL, Lemos-Marini SH, Silva RB, Marques-de-Faria AP, De Mello MP, Maciel-Guerra AT, Guerra-Junior G. De Paula GB, et al. Int J Endocrinol. 2016;2016:4963574. doi: 10.1155/2016/4963574. Epub 2016 Nov 28. Int J Endocrinol. 2016. PMID: 28018429 Free PMC article.
Gonadotropin-independent precocious puberty due to luteinizing hormone receptor mutations in Brazilian boys: a novel constitutively activating mutation in the first transmembrane helix.
Latronico AC, Shinozaki H, Guerra G Jr, Pereira MA, Lemos Marini SH, Baptista MT, Arnhold IJ, Fanelli F, Mendonca BB, Segaloff DL. Latronico AC, et al. J Clin Endocrinol Metab. 2000 Dec;85(12):4799-805. doi: 10.1210/jcem.85.12.7071. J Clin Endocrinol Metab. 2000. PMID: 11134146
Growth charts of Brazilian girls with Turner syndrome without the use of GH or oxandrolone.
Carpini-Dantas S, Guerra-Junior G, Maciel-Guerra AT, Marmo DB, Vieira TP, Lopes CP, Baptista MTM, Morcillo AM, de Lemos-Marini SHV. Carpini-Dantas S, et al. Among authors: de lemos marini shv. J Pediatr (Rio J). 2024 Oct 25:S0021-7557(24)00129-3. doi: 10.1016/j.jped.2024.09.003. Online ahead of print. J Pediatr (Rio J). 2024. PMID: 39489927 Free article.
Insights from a Wolfram syndrome cohort: clinical and molecular findings from a specialized diabetes reference center.
Lopes CP, Gonçalves GF, Paulino MFVM, Esquiaveto-Aun AM, de Mello MP, Pavin EJ, Breder ISS, Pu MZMH, de Lemos-Marini SHV, Guerra G. Lopes CP, et al. Among authors: de lemos marini shv. Arch Endocrinol Metab. 2024 Sep 24;68:e240091. doi: 10.20945/2359-4292-2024-0091. eCollection 2024. Arch Endocrinol Metab. 2024. PMID: 39420940 Free PMC article.
X-linked congenital adrenal hypoplasia: Report of long clinical follow-up and description of a new complex variant in the NR0B1 gene.
Esquiaveto-Aun AM, de Mello MP, Guaragna MS, da Silva Lopes VLG, Francese-Santos AP, Dos Santos Cruz Piveta C, Mazolla TN, de Lemos-Marini SHV, Guerra-Junior G. Esquiaveto-Aun AM, et al. Among authors: de lemos marini shv. Am J Med Genet A. 2024 Jun;194(6):e63536. doi: 10.1002/ajmg.a.63536. Epub 2024 Jan 19. Am J Med Genet A. 2024. PMID: 38243380
76 results