Browsing by Author Baptista, Maria Tereza Matias

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Showing results 1 to 19 of 19
PreviewIssue DateTitleAuthor(s)AdvisorType
1-Sep-2012Sexual difference, identification and object choice in individuals with sex differentiation disordersBley, Adriano Morad; Turato, Egberto Ribeiro; Rivorêdo, Carlos Roberto Soares Freire de; Silva, Roberto Benedito de Paiva e; Maciel-Guerra, Andrea Trevas; Marques-de-Faria, Antonia Paula; Guerra-Junior, Gil; Baptista, Maria Tereza Matias-Artigo de periódico
2008Xx Maleness And Xx True Hermaphroditism In Sry-negative Monozygotic Twins: Additional Evidence For A Common Origin.Maciel-Guerra, Andréa Trevas; de Mello, Maricilda Palandi; Coeli, Fernanda Boechers; Ribeiro, Marcelo Lima; Miranda, Márcio Lopes; Marques-de-Faria, Antonia Paula; Baptista, Maria Tereza Matias; Moraes, Suzana Guimarães; Guerra-Júnior, Gil-Artigo de periódico
2011Metabolic Evaluation Of Young Women With Congenital Adrenal Hyperplasia.Schnaider-Rezek, Gabrielle Sormanti; Lemos-Marini, Sofia Helena Valente de; Baptista, Maria Tereza Matias; Guerra-Júnior, Gil; Morcillo, André Moreno; Mello, Maricilda Palandi de; Oliveira, Laurione Cândido de; D'Souza-Li, Lilia-Artigo de periódico
2007Spontaneous Final Height In Turner's Syndrome In Brazil.de Lemos-Marini, Sofia Helena Valente; Morcillo, André Moreno; Baptista, Maria Tereza Matias; Guerra-Jr, Gil; Maciel-Guerra, Andréa Trevas-Artigo de periódico
2007Severe Rhabdomyolysis Due To Adipsic Hypernatremia After Craniopharyngioma Surgery.Zantut-Wittmann, Denise E; Garmes, Heraldo Mendes; Panzan, Anita Denardo; Lima, Marcelo de Oliveira; Baptista, Maria Tereza Matias-Artigo de periódico
2010Novel Dmrt1 3'utr+11inst Mutation Associated To Xy Partial Gonadal Dysgenesis.Mello, Maricilda Palandi de; Coeli, Fernanda Borchers; Assumpção, Juliana Godoy; Castro, Tammy Mazeo; Maciel-Guerra, Andréa Trevas; Marques-de-Faria, Antônia Paula; Baptista, Maria Tereza Matias; Guerra-Júnior, Gil-Artigo de periódico
2012Spontaneous Puberty In Girls With Early Diagnosis Of Turner Syndrome.Carpini, Stela; Carvalho, Annelise Barreto; Guerra-Júnior, Gil; Baptista, Maria Tereza Matias; Lemos-Marini, Sofia Helena Valente; Maciel-Guerra, Andréa Trevas-Artigo de periódico
2011Growth Hormone Effect On Body Composition In Turner Syndrome.Baldin, Alexandre Duarte; Fabbri, Tatiana; Siviero-Miachon, Adriana Aparecida; Spinola-Castro, Angela Maria; de Lemos-Marini, Sofia Helena Valente; Baptista, Maria Tereza Matias; D'Souza-Li, Lilia Freire Rodrigues; Maciel-Guerra, Andrea Trevas; Guerra-Junior, Gil-Artigo de periódico
-Cardiovascular And Renal Anomalies In Turner Syndrome.Carvalho, Annelise Barreto; Guerra Júnior, Gil; Baptista, Maria Tereza Matias; de Faria, Antonia Paula Marques; Marini, Sofia Helena Valente de Lemos; Guerra, Andréa Trevas Maciel-Artigo de periódico
2010Long-term Follow-up Of An 8-year-old Boy With Insulinoma As The First Manifestation Of A Familial Form Of Multiple Endocrine Neoplasia Type 1.Fabbri, Helena Campos; Mello, Maricilda Palandi de; Soardi, Fernanda Caroline; Esquiaveto-Aun, Adriana Mangue; Oliveira, Daniel Minutti de; Denardi, Fernanda Canova; Moura-Neto, Arnaldo; Garmes, Heraldo Mendes; Baptista, Maria Tereza Matias; Matos, Patrícia Sabino de; Lemos-Marini, Sofia Helena Valente de; D'Souza-Li, Lilia Freire Rodrigues; Guerra-Júnior, Gil-Artigo de periódico
2010Six New Cases Confirm The Clinical Molecular Profile Of Complete Combined 17α-hydroxylase/ 17,20-lyase Deficiency In Brazil.Belgini, Daiane Rodrigues Barbosa; Mello, Maricilda Palandi de; Baptista, Maria Tereza Matias; Oliveira, Daniel Minutti de; Denardi, Fernanda Canova; Garmes, Heraldo Mendes; Grassiotto, Oswaldo da Rocha; Benetti Pinto, Cristina Laguna; Marques-de-Faria, Antonia Paula; Maciel-Guerra, Andréa Trevas; Guerra-Júnior, Gil-Artigo de periódico
1-Nov-2011Metabolic evaluation of young women with congenital adrenal hyperplasiaSchnaider-Rezek, Gabrielle Sormanti; Lemos-Marini, Sofia Helena Valente de; Baptista, Maria Tereza Matias; Guerra-Júnior, Gil; Morcillo, André Moreno; Mello, Maricilda Palandi de; Oliveira, Laurione Cândido de; D'Souza-Li, Lilia-Artigo de periódico
1-Nov-2010Long-term follow-up of an 8-year-old boy with insulinoma as the first manifestation of a familial form of multiple endocrine neoplasia type 1Fabbri, Helena Campos; Mello, Maricilda Palandi de; Soardi, Fernanda Caroline; Esquiaveto-Aun, Adriana Mangue; Oliveira, Daniel Minutti de; Denardi, Fernanda Canova; Moura-Neto, Arnaldo; Garmes, Heraldo Mendes; Baptista, Maria Tereza Matias; Matos, Patrícia Sabino de; Lemos-Marini, Sofia Helena Valente de; D'Souza-Li, Lilia Freire Rodrigues; Guerra-Júnior, Gil-Artigo de periódico
1-Nov-2010Six new cases confirm the clinical molecular profile of complete combined 17α-hydroxylase/ 17,20-lyase deficiency in BrazilBelgini, Daiane Rodrigues Barbosa; Mello, Maricilda Palandi de; Baptista, Maria Tereza Matias; Oliveira, Daniel Minutti de; Denardi, Fernanda Canova; Garmes, Heraldo Mendes; Grassiotto, Oswaldo da Rocha; Benetti Pinto, Cristina Laguna; Marques-de-Faria, Antonia Paula; Maciel-Guerra, Andréa Trevas; Guerra-Júnior, Gil-Artigo de periódico
1-Nov-2010Novel DMRT1 3'UTR+11insT mutation associated to XY partial gonadal dysgenesisMello, Maricilda Palandi de; Coeli, Fernanda Borchers; Assumpção, Juliana Godoy; Castro, Tammy Mazeo; Maciel-Guerra, Andréa Trevas; Marques-de-Faria, Antônia Paula; Baptista, Maria Tereza Matias; Guerra-Júnior, Gil-Artigo de periódico
1-Dec-2012Spontaneous puberty in girls with early diagnosis of Turner syndromeCarpini, Stela; Carvalho, Annelise Barreto; Guerra-Júnior, Gil; Baptista, Maria Tereza Matias; Lemos-Marini, Sofia Helena Valente; Maciel-Guerra, Andréa Trevas-Artigo de periódico
1-Jan-2010Cardiovascular and renal anomalies in Turner syndromeCarvalho, Annelise Barreto; Guerra Júnior, Gil; Baptista, Maria Tereza Matias; Faria, Antonia Paula Marques de; Marini, Sofia Helena Valente de Lemos; Guerra, Andréa Trevas Maciel-Artigo de periódico
2010Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1Trarbach, Ericka Barbosa; Teles, Milena Gurgel; Costa, Elaine Maria Frade; Abreu, Ana Paula; Garmes, Heraldo Mendes; Guerra, Gil; Baptista, Maria Tereza Matias; Castro, Margaret de; Mendonca, Berenice Bilharinho; Latronico, Ana Claudia-Artigo
2008Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive kallmann syndromeAbreu, Ana Paula; Trarbach, Ericka Barbosa; Castro, Margaret de; Costa, Elaine Maria Frade; Versiani, Beatriz; Baptista, Maria Tereza Matias; Garmes, Heraldo Mendes; Mendonca, Berenice Bilharinho; Latronico, Ana Claudia-Artigo
Showing results 1 to 19 of 19