Browsing by Author Maciel-Guerra, AT

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PreviewIssue DateTitleAuthor(s)AdvisorType
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
2012Clinical and molecular spectrum of patients with 17 beta-hydroxysteroid dehydrogenase type 3 (17-beta-HSD3) deficiencyCastro, CCTD; Guaragna, G; Calais, FL; Coeli, FB; Leal, IRL; Cavalcante, EF; Monlleo, IL; Pereira, SRF; Silva, RBDE; Gabiatti, JRE; Marques-de-Faria, AP; Maciel-Guerra, AT; De Mello, MP; Guerra, G-Artigo de periódico
2003Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a cross-sectional study of factors involved in bone mineral densityFreire, POD; De Lemos-Marini, SHV; Maciel-Guerra, AT; Morcillo, AM; Baptista, MTM; de Mello, MP; Guerra, G-Artigo de periódico
2012Clinical and Laboratorial Features That May Differentiate 46,XY DSD due to Partial Androgen Insensitivity and 5 alpha-Reductase Type 2 DeficiencyVeiga, NN; Medaets, PAR; Petroli, RJ; Calais, FL; de Mello, MP; Castro, CCTDS; Guaragna, G; Sewaybricker, LE; Marques-de-Faria, AP; Maciel-Guerra, AT; Guerra, G-Artigo de periódico
2008Congenital perineal lipoma presenting as ambiguous genitaliaGuerra, G; Aun, AME; Miranda, ML; Beraldo, LP; Moraes, SG; Baptista, MTM; Marques-de-Faria, AP; Maciel-Guerra, AT-Artigo de periódico
2011Complete gonadal dysgenesis in clinical practice: the 46,XY karyotype accounts for more than one third of casesRocha, VBC; Guerra, G; Marques-de-Faria, AP; de Mello, MP; Maciel-Guerra, AT-Artigo de periódico
2013Two distinct WT1 mutations identified in patients and relatives with isolated nephrotic proteinuriaGuaragna, MS; Lutaif, ACGB; Piveta, CSC; Belangero, VMS; Maciel-Guerra, AT; Guerra, G; De Mello, MP-Artigo de periódico
2000A boy with mental retardation, blepharophimosis and hypothyroidism: a diagnostic dilemma between Young-Simpson and Ohdo syndromeMarques-de-Faria, AP; Maciel-Guerra, AT; Junior, GG; Baptista, MTM-Artigo de periódico
2008An illustrative case of Leri-Weill dyschondrosteosisde Lima, R; Iamada, CF; Silva, LO; de Mello, MP; Maciel-Guerra, AT-Artigo de periódico
2013Screening of Y chromosome microdeletions in 46,XY partial gonadal dysgenesis and in patients with a 45,X/46,XY karyotype or its variantsdos Santos, AP; Andrade, JGR; Piveta, CSC; de Paulo, J; Guerra, G; de Mello, MP; Maciel-Guerra, AT-Artigo de periódico
2011Growth hormone effect on body composition in Turner syndromeBaldin, AD; Fabbri, T; Siviero-Miachon, AA; Spinola-Castro, AM; de Lemos-Marini, SHV; Baptista, MTM; D'Souza-Li, LFR; Maciel-Guerra, AT; Guerra, G-Artigo de periódico
2006A rare case of aniridia and balanced translocation (5;11) (p15.3; q22) arising in the same subject: A challenge for genetic counselingVulcan-Freitas, TM; Maciel-Guerra, AT-Artigo de periódico
2010Complete XY gonadal dysgenesis due to p.D293N homozygous mutation in the NR5A1 gene: a case studySoardi, FC; Coeli, FB; Maciel-Guerra, AT; Guerra, G; de Mello, MP-Artigo de periódico
2006Infertility and marker chromosomes: Application of molecular cytogenetic techniques in a case of inv dup(15)Vulcani-Freitas, TM; Gil-Da-Silva-Lopes, VL; Varella-Garcia, M; Maciel-Guerra, AT-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
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
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
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
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