Browsing by Author Baptista, MTM

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PreviewIssue DateTitleAuthor(s)AdvisorType
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
2006Novel fibroblast growth factor receptor 1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmiaTrarbach, EB; Costa, EMF; Versiani, B; de Castro, M; Baptista, MTM; Garmes, HM; de Mendonca, BB; Latronico, AC-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
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
2005Molecular analysis of KAL-1, GnRH-R, NELF and EBF2 genes in a series of Kallmann syndrome and normosmic hypogonadotropic hypogonadism patientsTrarbach, EB; Baptista, MTM; Garmes, HM; Hackel, C-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
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
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
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
2009Impairment in Anthropometric Parameters and Body Composition in Females with Classical 21-Hydroxylase DeficiencyGoncalves, EM; de Lemos-Marini, SHV; de Mello, MP; Baptista, MTM; D'Souza-Li, LFR; Baldin, AD; Carvalho, WRG; Farias, ES; Guerra, G-Artigo de periódico
2000Gonadotropin-independent precocious puberty due to luteinizing hormone receptor mutations in Brazilian boys: A novel constitutively activating mutation in the first transmembrane helixLatronico, AC; Shinozaki, H; Guerra, G; Pereira, MAA; Marini, SHVL; Baptista, MTM; Arnhold, IJP; Fanelli, F; Mendonca, BB; Segaloff, DL-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
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
2012Turner syndrome and metabolic derangements: Another example of fetal programmingBaldin, AD; Siviero-Miachon, AA; Fabbri, T; de Lemos-Marini, SHV; Spinola-Castro, AM; Baptista, MTM; D'Souza-Li, LFR; Morcillo, AM; Maciel-Guerra, AT; Guerra, G-Artigo de periódico