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Partial remission in Brazilian children and adolescents with type 1 diabetes. Association with a haplotype of class II human leukocyte antigen and synthesis of autoantibodies.
Camilo DS, Pradella F, Paulino MF, Baracat ECE, Marini SH, Guerra G Jr, Pavin EJ, Parisi C, Longhini ALF, Marques SB, Guariento EG, Lieber SR, Macedo CF, Gama E Silva L, Farias AS, Santos LMB, Volpini WMG. Camilo DS, et al. Among authors: guerra g jr. Pediatr Diabetes. 2020 Jun;21(4):606-614. doi: 10.1111/pedi.12999. Epub 2020 Mar 6. Pediatr Diabetes. 2020. PMID: 32078220
A Single Nucleotide Variant in the Promoter Region of 17β-HSD Type 5 Gene Influences External Genitalia Virilization in Females with 21-Hydroxylase Deficiency.
Kaupert LC, Gomes LG, Brito VN, Lemos-Marini SH, de Mello MP, Longui CA, Kochi C, de Castro M, Guerra G Jr, Mendonca BB, Bachega TA. Kaupert LC, et al. Among authors: guerra g jr. Horm Res Paediatr. 2016;85(5):333-8. doi: 10.1159/000445684. Epub 2016 Apr 16. Horm Res Paediatr. 2016. PMID: 27082632 Clinical Trial.
Performance of phalangeal quantitative ultrasound parameters in the evaluation of reduced bone mineral density assessed by DX in patients with 21 hydroxylase deficiency.
Gonçalves EM, Sewaybricker LE, Baptista F, Silva AM, Carvalho WR, Santos AO, de Mello MP, Lemos-Marini SH, Guerra G Jr. Gonçalves EM, et al. Among authors: guerra g jr. Ultrasound Med Biol. 2014 Jul;40(7):1414-9. doi: 10.1016/j.ultrasmedbio.2013.12.027. Epub 2014 Apr 13. Ultrasound Med Biol. 2014. PMID: 24726797
OCT4 immunohistochemistry may be necessary to identify the real risk of gonadal tumors in patients with Turner syndrome and Y chromosome sequences.
Barros BA, Moraes SG, Coeli FB, Assumpção JG, De Mello MP, Maciel-Guerra AT, Carvalho AB, Viguetti-Campos N, Vieira TA, Amstalden EM, Andrade JG, Esquiaveto-Aun AM, Marques-de-Faria AP, D'Souza-Li LF, Lemos-Marini SH, Guerra G Jr. Barros BA, et al. Among authors: guerra g jr. Hum Reprod. 2011 Dec;26(12):3450-5. doi: 10.1093/humrep/der310. Epub 2011 Sep 19. Hum Reprod. 2011. PMID: 21930534
Growth hormone pharmacogenetics: the interactive effect of a microsatellite in the IGF1 promoter region with the GHR-exon 3 and -202 A/C IGFBP3 variants on treatment outcomes of children with severe GH deficiency.
Costalonga EF, Antonini SR, Guerra G Jr, Coletta RR, Franca MM, Braz AF, Mendonca BB, Arnhold IJ, Jorge AA. Costalonga EF, et al. Among authors: guerra g jr. Pharmacogenomics J. 2012 Oct;12(5):439-45. doi: 10.1038/tpj.2011.13. Epub 2011 Apr 5. Pharmacogenomics J. 2012. PMID: 21468024
29 results