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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
DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis.
de Oliveira FR, Mazzola TN, de Mello MP, Francese-Santos AP, Lemos-Marini SHV, Maciel-Guerra AT, Hiort O, Werner R, Guerra-Junior G, Fabbri-Scallet H. de Oliveira FR, et al. Among authors: lemos marini shv. Life (Basel). 2023 Apr 27;13(5):1093. doi: 10.3390/life13051093. Life (Basel). 2023. PMID: 37240737 Free PMC article.
Sex dimorphism of weight and length at birth: evidence based on disorders of sex development.
Amais DSR, da Silva TER, Barros BA, de Andrade JGR, de Lemos-Marini SHV, de Mello MP, Marques-de-Faria AP, Mazzola TN, Guaragna MS, Fabbri-Scallet H, Vieira TAP, Viguetti-Campos NL, Morcillo AM, Hiort O, Maciel-Guerra AT, Guerra-Junior G. Amais DSR, et al. Among authors: de lemos marini shv. Ann Hum Biol. 2022 Dec;49(7-8):274-279. doi: 10.1080/03014460.2022.2134452. Epub 2023 Jan 23. Ann Hum Biol. 2022. PMID: 36218438
Normal ambulatory blood pressure in young adults with 21-hydroxylase enzyme deficiency undergoing glucocorticoid replacement therapy.
Borges JH, Camargo DA, Sewaybricker LE, Santoro RI, de Oliveira DM, de Lemos-Marini SHV, Geloneze B, Guerra G Júnior, Gonçalves EM. Borges JH, et al. Among authors: de lemos marini shv. Arch Endocrinol Metab. 2023 Jan 18;67(1):64-72. doi: 10.20945/2359-3997000000504. Epub 2022 Aug 4. Arch Endocrinol Metab. 2023. PMID: 35929901 Free PMC article.
74 results