Browsing by Author Guerra, G

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

or enter first few letters:  
Showing results 1 to 20 of 64  next >
PreviewIssue DateTitleAuthor(s)AdvisorType
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
2000Beckwith-Wiedemann syndrome and virilizing cortical adrenal tumor in a childSbragia-Neto, L; Melo, AA; Guerra, G; Marini, SHVD; Baptista, MTM; de Matos, PS; de Oliveira, AG; Bustorff-Silva, JM-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
2005Adrenocortical tumors in Brazilian children - Immunohistochemical markers and prognostic factorsSbragia, L; Oliveira, AG; Vassallo, J; Pinto, GA; Guerra, G; Bustorff-Silva, J-Artigo de periódico
1997Female Pseudohermaphroditism Due To Classical 21-hydroxylase Deficiency In A Girl With Turner Syndrome.Maciel-Guerra, A T; Guerra, G; Marini, S H; Matias Baptista, M T; Marques-de-Faria, A P-Artigo de periódico
1998Detection Of Gly-196-ser Mutation In 5alpha-reductase Type Ii Gene In A Brazilian Patient With Female Assignment And Behavior.Caldas Ferraz, L F; Guerra, G; Matias Baptista, M T; Maciel-Guerra, A T; Hackel, C-Artigo de periódico
1996Molecular Analysis Of Cyp21 And C4 Genes In Brazilian Families With The Classical Form Of Steroid 21-hydroxylase Deficiency.de-Araujo, M; Sanches, M R; Suzuki, L A; Guerra, G; Farah, S B; de-Mello, M P-Artigo de periódico
1999Mutation Distribution And Cyp21/c4 Locus Variability In Brazilian Families With The Classical Form Of The 21-hydroxylase Deficiency.Paulino, L C; Araujo, M; Guerra, G; Marini, S H; De Mello, M P-Artigo de periódico
2000Turner's Syndrome And Thyroid Disease: A Transverse Study Of Pediatric Patients In Brazil.Medeiros, C C; Marini, S H; Baptista, M T; Guerra, G; Maciel-Guerra, A T-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 Population.Volpini, W M; Testa, G V; Marques, S B; Alves, L I; Silva, M E; Dib, S A; Guerra, G; Paulino, M F; Marini, S H; Persoli, L B; 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 Sequences.Barros, B A; Moraes, S G; Coeli, F B; Assumpção, J G; De Mello, M P; Maciel-Guerra, A T; Carvalho, A B; Viguetti-Campos, N; Vieira, T A P; Amstalden, E M I; Andrade, J G R; Esquiaveto-Aun, A M; Marques-de-Faria, A P; D'Souza-Li, L F R; Lemos-Marini, S H V; 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 Phenotypes.Assumpção, J G; Benedetti, C E; Maciel-Guerra, A T; Guerra, G; Baptista, M T M; Scolfaro, M R; de Mello, M P-Artigo de periódico
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
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
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
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
2008DIABETIC KETOACIDOSIS IN CHILDREN: TREATMENT PROFILE AT A UNIVERSITY HOSPITALCastro, L; Morcillo, AM; 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
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