Browsing by Author Lemos-Marini, SHV

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Showing results 1 to 13 of 13
PreviewIssue DateTitleAuthor(s)AdvisorType
2011OCT4 immunohistochemistry may be necessary to identify the real risk of gonadal tumors in patients with Turner syndrome and Y chromosome sequencesBarros, BA; Moraes, SG; Coeli, FB; Assumpcao, JG; De Mello, MP; Maciel-Guerra, AT; Carvalho, AB; Viguetti-Campos, N; Vieira, TAP; Amstalden, EMI; Andrade, JGR; Esquiaveto-Aun, AM; Marques-de-Faria, AP; D'Souza-Li, LFR; Lemos-Marini, SHV; Guerra, G-Artigo de periódico
2008Inhibition of CYP21A2 enzyme activity caused by novel missense mutations identified in Brazilian and Scandinavian patientsSoardi, FC; Barbaro, M; Lau, IF; Lemos-Marini, SHV; Baptista, MTM; Guerra-Junior, G; Wedell, A; Lajic, S; de Mello, MP-Artigo de periódico
2001H28+C insertion in the CYP21 gene: A novel frameshift mutation in a Brazilian patient with the classical form of 21-hydroxylase deficiencyLau, IF; Soardi, FC; Lemos-Marini, SHV; Guerra, G; Baptista, MTM; De Mello, MP-Artigo de periódico
2010Effects of growth hormone on body proportions in Turner syndrome compared with non-treated patients and normal womenBaldin, AD; Fabbri, T; Siviero-Miachon, AA; Spinola-Castro, AM; Lemos-Marini, SHV; Baptista, MTM; D'Souza-Li, LFR; Maciel-Guerra, AT; Guerra, G-Artigo de periódico
2013Estimation of percent body fat based on anthropometric measurements in children and adolescents with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyGoncalves, EM; Silva, AM; Matias, CN; Lemos-Marini, SHV; Santos, AO; Guerra, G-Artigo de periódico
2004Inhibin alpha-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriersLongui, CA; Lemos-Marini, SHV; Figueiredo, B; Mendonca, BB; Castro, M; Liberatore, R; Watanabe, C; Lancellotti, CLP; Rocha, MN; Melo, MB; Monte, O; Calliari, LEP; Guerra, G; Baptista, MTM; Sbragia-Neto, L; Latronico, AC; Moreira, A; Tardelli, AMD; Nigri, A; Taymans, SE; Stratakis, CA-Artigo de periódico
2002Bone mineralization in Turner syndrome: a transverse study of the determinant factors in 58 patientsCosta, AMG; Lemos-Marini, SHV; Baptista, MTM; Morcillo, AM; Maciel-Guerra, AT; Guerra, G-Artigo de periódico
2013The effect of fetal androgen metabolism-related gene variants on external genitalia virilization in congenital adrenal hyperplasiaKaupert, LC; Lemos-Marini, SHV; De Mello, MP; Moreira, RP; Brito, VN; Jorge, AAL; Longui, CA; Guerra, G; Mendonca, BB; Bachega, TA-Artigo de periódico
2003Validity of the use of a few hand-wrist bones for assessing bone ageGuimarey, L; Morcillo, AM; Orazi, V; Lemos-Marini, SHV-Artigo de periódico
200821-hydroxylase deficiency transiently mimicking combined 21- and 11 beta-hydroxylase deficiencyTonetto-Fernandes, V; Lemos-Marini, SHV; De Mello, MP; Ribeiro, LM; Kater, CE-Artigo de periódico
2004Labioscrotal island flap in feminizing genitoplastyMiranda, ML; de Oliveira, AG; Lemos-Marini, SHV-Artigo de periódico
2012Accuracy of anthropometric measurements in estimating fat mass in individuals with 21-hydroxylase deficiencyGoncalves, EM; Silva, AM; Santos, DA; Lemos-Marini, SHV; Santos, AD; Mendes-dos-Santos, CT; De-Mello, MP; Guerra, G-Artigo de periódico
2006Serum 21-deoxycortisol, 17-hydroxyprogesterone, and 11-deoxycortisol in classic congenital adrenal hyperplasia: Clinical and hormonal correlations and identification of patients with 11 beta-hydroxylase deficiency among a large group with alleged 21-hydroxylase deficiencyTonetto-Fernandes, V; Lemos-Marini, SHV; Kuperman, H; Ribeiro-Neto, LM; Verreschi, ITN; Kater, CE-Artigo de periódico