Browsing by Author Maciel-Guerra, AT

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PreviewIssue DateTitleAuthor(s)AdvisorType
2011Mutations for Leber hereditary optic neuropathy in patients with alcohol and tobacco optic neuropathyAmaral-Fernandes, MS; Marcondes, AM; Miranda, PMDD; Maciel-Guerra, AT; Sartorato, EL-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
2002Deafness resulting from mutations in the GJB2 (connexin 26) gene in Brazilian patientsOliveira, CA; Maciel-Guerra, AT; Sartorato, EL-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
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
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
2010Leber's hereditary optic neuropathy: Clinical and molecular profile of a Brazilian sampleMaciel-Guerra, AT; Zanchetta, LM; Fernandes, MSA; Andrade, PB; Miranda, PMDD; Sartorato, EL-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
1999New frameshift mutation in the 5 alpha-reductase type 2 gene in a Brazilian patient with 5 alpha-reductase deficiencyFerraz, LFC; Baptista, MTM; Maciel-Guerra, AT; Junior, GG; Hackel, C-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
2005A naturally occurring deletion in the SRY promoter region affecting the Sp1 binding site is associated with sex reversalAssumpcao, JG; Ferraz, LFC; Benedetti, CE; Maciel-Guerra, AT; Guerra, G; Marques-de-Faria, AP; Baptista, TM; de Mello, MP-Artigo de periódico
2007Spontaneous final height in Turner's syndrome in Brazilde Lemos-Marini, SHV; Morcillo, AM; Matias Baptista, MT; Guerra, G; Maciel-Guerra, AT-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
2004Frequency of the 35delG mutation in the GJB2 gene in samples of European, Asian, and African BraziliansOliveira, CA; Alexandrino, E; Abe-Sandes, K; Silva, WA; Maciel-Guerra, AT; Magna, LA; Sartorato, EL-Artigo de periódico
2014The novel p.Cys65Tyr mutation in NR5A1 gene in three 46,XY siblings with normal testosterone levels and their mother with primary ovarian insufficiencyFabbri, HC; de Andrade, JGR; Soardi, FC; de Calais, FL; Petroli, RJ; Maciel-Guerra, AT; Guerra-Junior, G; de Mello, MP-Artigo de periódico
2008XX maleness and XX true hermaphroditism in SRY-negative monozygotic twins: Additional evidence for a common originMaciel-Guerra, AT; de Mello, MP; Coeli, FB; Ribeiro, ML; Miranda, ML; Marques-De-Faria, AP; Baptista, MTM; Moraes, SGE; Guerra-Junior, G-Artigo de periódico
2009Turner's Syndrome and Subclinical Autoimmune Thyroid Disease: A Two-Year Follow-up StudyMedeiros, CCM; de Lemos-Marini, SHV; Bricola, M; Camargo, EE; Santos, AO; Magna, LA; Guerra, G; Baptista, MTM; Maciel-Guerra, AT-Artigo de periódico