Browsing by Author de Mello, Maricilda Palandi

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Showing results 1 to 13 of 13
PreviewIssue DateTitleAuthor(s)AdvisorType
2015Hyperprolactinemia In Children And Adolescents With Use Of Risperidone: Clinical And Molecular Genetics Aspects.Dos Santos Júnior, Amilton; Henriques, Taciane Barbosa; de Mello, Maricilda Palandi; Neto, Adriana Perez Ferreira; Paes, Lúcia Arisaka; Torre, Osmar Henrique Della; Sewaybricker, Letícia Esposito; Fontana, Thiago Salum; Celeri, Eloisa Helena Rubello Valler; Júnior, Gil Guerra; Dalgalarrondo, Paulo-Artigo de periódico
2013New Mutation In The Myocilin Gene Segregates With Juvenile-onset Open-angle Glaucoma In A Brazilian Family.Braghini, Carolina Ayumi; Neshich, Izabella Agostinho Pena; Neshich, Goran; Soardi, Fernanda Caroline; de Mello, Maricilda Palandi; Costa, Vital Paulino; de Vasconcellos, José Paulo Cabral; de Melo, Mônica Barbosa-Artigo de periódico
2012Clinical And Laboratorial Features That May Differentiate 46,xy Dsd Due To Partial Androgen Insensitivity And 5α-reductase Type 2 Deficiency.Veiga-Junior, Nélio Neves; Medaets, Pedro Augusto Rodrigues; Petroli, Reginaldo José; Calais, Flávia Leme; de Mello, Maricilda Palandi; Castro, Carla Cristina Telles de Sousa; Guaragna-Filho, Guilherme; Sewaybricker, Letícia Espósito; Marques-de-Faria, Antonia Paula; Maciel-Guerra, Andréa Trevas; Guerra-Junior, Gil-Artigo de periódico
1-Nov-2010Phenotypic variability in a family with x-linked adrenoleukodystrophy caused by the p.Trp132Ter mutationSoardi, Fernanda Caroline; Esquiaveto-Aun, Adriana Mangue; Guerra-Júnior, Gil; Lemos-Marini, Sofia Helena Valente de; de Mello, Maricilda Palandi-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
2011Molecular Diagnosis Of 5α-reductase Type Ii Deficiency In Brazilian Siblings With 46,xy Disorder Of Sex Development.Leme de Calais, Flávia Leme; Soardi, Fernanda Caroline; Petroli, Reginaldo José; Lusa, Ana Letícia Gori; de Paiva E Silva, Roberto Benedito; Maciel-Guerra, Andréa Trevas; Guerra-Júnior, Gil; de Mello, Maricilda Palandi-Artigo de periódico
2010The Novel Wt1 Gene Mutation P.h377n Associated To Denys-drash Syndrome.Guaragna, Mara Sanches; Soardi, Fernanda Caroline; Assumpção, Juliana Godoy; Zambaldi, Lílian de Jesus Girotto; Cardinalli, Izilda Aparecida; Yunes, José Andrés; de Mello, Maricilda Palandi; Brandalise, Silvia Regina; Aguiar, Simone dos Santos-Artigo de periódico
2014Long-term Follow-up Of Patients With 46,xy Partial Gonadal Dysgenesis Reared As Males.Gabriel Ribeiro de Andrade, Juliana; Marques-de-Faria, Antonia Paula; Fabbri, Helena Campos; de Mello, Maricilda Palandi; Guerra-Júnior, Gil; Maciel-Guerra, Andréa Trevas-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 Insufficiency.Fabbri, Helena Campos; de Andrade, Juliana Gabriel Ribeiro; Soardi, Fernanda Caroline; de Calais, Flávia Leme; Petroli, Reginaldo José; Maciel-Guerra, Andréa Trevas; Guerra-Júnior, Gil; de Mello, Maricilda Palandi-Artigo de periódico
2006Q289p Mutation In Fgfr2 Gene Causes Saethre-chotzen Syndrome: Some Considerations About Familial Heterogeneity.Freitas, Erika Cristina Lopes Burrone de; Nascimento, Sandra Regina Dantas; de Mello, Maricilda Palandi; Gil-da-Silva-Lopes, Vera Lúcia-Artigo de periódico
2003Classical Congenital Adrenal Hyperplasia Due To 21-hydroxylase Deficiency: A Cross-sectional Study Of Factors Involved In Bone Mineral Density.de Almeida Freire, Patrícia Oliveira; de Lemos-Marini, Sofia Helena Valente; Maciel-Guerra, Andréa Trevas; Morcillo, André Moreno; Matias Baptista, Maria Tereza; de Mello, Maricilda Palandi; Guerra, Gil-Artigo de periódico
2011Severe Forms Of Partial Androgen Insensitivity Syndrome Due To P.l830f Novel Mutation In Androgen Receptor Gene In A Brazilian Family.Petroli, Reginaldo J; Maciel-Guerra, Andréa T; Soardi, Fernanda C; de Calais, Flávia L; Guerra-Junior, Gil; de Mello, Maricilda Palandi-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 Variants.dos Santos, Ana Paula; Andrade, Juliana Gabriel Ribeiro; Piveta, Cristiane Santos Cruz; de Paulo, Juliana; Guerra, Gil; de Mello, Maricilda Palandi; Maciel-Guerra, Andréa Trevas-Artigo de periódico