Browsing by Author Guerra, G

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PreviewIssue DateTitleAuthor(s)AdvisorType
1999Mutation distribution and CYP21/C4 locus variability in Brazilian families with the classical form of the 21-hydroxylase deficiencyPaulino, LC; Araujo, M; Guerra, G; Marini, SHVL; De Mello, MP-Artigo de periódico
1998Detection of Gly-196-Ser mutation in 5 alpha-reductase type II gene in a Brazilian patient with female assignment and behaviorFerraz, LFC; Guerra, G; Baptista, MTM; Maciel-Guerra, AT; Hackel, C-Artigo de periódico
1997Female pseudohermaphroditism due to classical 21-hydroxylase deficiency in a girl with Turner syndromeMacielGuerra, AT; Guerra, G; Marini, SHVL; Baptista, MTM; MarquesdeFaria, AP-Artigo de periódico
2001Family-based association of HLA class II alleles and haplotypes with type I diabetes in Brazilians reveals some characteristics of a highly diversified populationVolpini, WMG; Testa, GV; Marques, SBD; Alves, LI; Silva, MER; Dib, SA; Guerra, G; Paulino, MFVM; Marini, SHVL; Persoli, LBL; Caillat-Zucman, S-Artigo de periódico
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
2008DIABETIC KETOACIDOSIS IN CHILDREN: TREATMENT PROFILE AT A UNIVERSITY HOSPITALCastro, L; Morcillo, AM; Guerra, G-Artigo de periódico
2005Diagnosis of 5 alpha-reductase type 2 deficiency: Contribution of anti-Mullerian hormone evaluationStuchi-Perez, EG; Hackel, C; Oliveira, LEC; Ferraz, LFC; Oliveira, LC; Nunes-Silva, D; Toralles, MB; Steinmetz, L; Damiani, D; Maciel-Guerra, AT; Guerra, G-Artigo de periódico
2002Novel mutations affecting SRY DNA-binding activity: the HMG box N65H associated with 46,XY pure gonadal dysgenesis and the familial non-HMG box R30I associated with variable phenotypesAssumpcao, JG; Benedetti, CE; Maciel-Guerra, AT; Guerra, G; Baptista, MTM; Scolfaro, MR; de Mello, MP-Artigo de periódico
2010Novel DMRT1 3 ' UTR+11insT mutation associated to XY partial gonadal dysgenesisde Mello, MP; Coeli, FB; Assumpcao, JG; Castro, TM; Maciel-Guerra, AT; Marques-de-Faria, AP; Baptista, MTM; Guerra, G-Artigo de periódico
2009Mutations in NR5A1 Associated with Ovarian InsufficiencyLourenco, D; Brauner, R; Lin, L; De Perdigo, A; Weryha, G; Muresan, M; Boudjenah, R; Guerra, G; Maciel-Guerra, AT; Achermann, JC; McElreavey, K; Bashamboo, A-Artigo de periódico
2010Nobel deletion alleles carrying CYP21A1P/A2 chimeric genes in Brazilian patients with 21-hydroxylase deficiencyCoeli, FB; Soardi, FC; Bernardi, RD; de Araujo, M; Paulino, LC; Lau, IF; Petroli, RJ; de Lemos-Marini, SHV; Baptista, MTM; Guerra, G; de-Mello, MP-Artigo de periódico
2013Cross-sectional study of the association of body composition and physical fitness with bone status in children and adolescents from 11 to 16 years oldde Moraes, AM; Goncalves, EM; Barbeta, VJD; Guerra, G-Artigo de periódico
2011Molecular Diagnosis of 5 alpha-Reductase Type II Deficiency in Brazilian Siblings with 46,XY Disorder of Sex Developmentde Calais, FL; Soardi, FC; Petroli, RJ; Lusa, ALG; Silva, RBDE; Maciel-Guerra, AT; Guerra, G; de Mello, MP-Artigo de periódico
1996Molecular analysis of CYP21 and C4 genes in Brazilian families with the classical form of steroid 21-hydroxylase deficiencydeAraujo, M; Sanches, MR; Suzuki, LA; Guerra, G; Farah, SB; deMello, 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
2000Evaluation of the tubular and interstitial functions of the testis in 46,XY patients with ambiguous genitaliaStuchi-Perez, EG; Lukas-Croisier, C; De Castro, M; Baptista, MTM; Scolfaro, MR; Marques-De-Faria, AP; Hackel, C; Maciel-Guerra, AT; Guerra, G-Artigo de periódico
1996Coexistence of ovotestis and testicular regression in a boy with 46,XX/46,XY chimerism and sex ambiguityMacielGuerra, AT; Lopes, VLGD; Cardinalli, IA; Viguetti, NL; MarquesDeFaria, AP; Baptista, MTM; Guerra, G-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